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USMLE 2CK - Goljan High-Yield

Quiz yourself by thinking what should be in each of the black spaces below before clicking on it to display the answer.
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Question
Answer
PO2   driving force for diffusion of O2 into tissue  
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SaO2   percent heme groups occupied by O2  
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Cyanosis   decreased O2 saturation (SaO2); O2 content  
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Oxygen   electron acceptor in oxidative pathway  
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Hypoxia   inadequate O2 leads to ATP depletion  
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Ischemia   decreased arterial (or venous) blood flow  
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Respiratory acidosis   retention of CO, always decreases PaO2  
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Ventilation defect   impaired delivery of O2 to alveoli; intrapulmonary shunting of blood (e.g., RDS)  
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Perfusion defect   absent blood flow to alveoli; increased alveolar dead space (e.g., pulmonary embolus)  
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Diffusion defect   O2 cannot cross alveolar-capillary interface; interstitial lung disease (e.g., sarcoidosis)  
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Methemoglobin   ↓ SaO2; heme Fe+3; oxidizing agents (sulfur/nitro drugs); Rx with IV methylene blue  
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Clinical methemoglobinemia   cyanosis not corrected by O2; chocolate colored blood  
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Carbon monoxide   ↓ SaO2; left-shift O2 binding curve; inhibits cytochrome oxidase  
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Causes carbon monoxide poisoning   car exhaust, space heaters, smoke inhalation  
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S/S carbon monoxide poisoning   headache; cherry red color skin  
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Cyanide   inhibits cytochrome oxidase; systemic asphyxiant  
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Carbon monoxide + cyanide poisoning   house fires  
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Left-shifted O2 curve   ↓ 2, 3 BPG, carbon monoxide, alkalosis, HbF, methemoglobin, hypothermia  
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Right-shifted O2 curve   ↑ 2, 3 BPG, high altitude, acidosis, fever  
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High altitude   respiratory alkalosis enhances glycolysis; ↑ synthesis 2,3 BPG  
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Mitochondrial poisons   damages membrane and drains off protons; alcohol, salicylates  
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Uncoupling agents in mitochondria   drain off protons; dinitrophenol, thermogenin (brown fat)  
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Complication mitochondrial poisons/uncoupling agents   hyperthermia  
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Decreased ATP   impaired Na+/K+ ATPase pump (cellular swelling); reversible  
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Anaerobic glycolysis   ATP synthesis in hypoxia; lactate ↓ intracellular pH, denatures proteins  
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Irreversible injury hypoxia   membrane/mitochondrial damage  
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Mitochondrial damage   release cytochrome c activates apoptosis  
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Irreversible injury hypoxia   ↑ cytosolic Ca2+ activates phospholipase, proteases, endonuclease  
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Free radicals   unpaired electron in outer orbit; damage cell membranes and DNA  
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Free radicals   superoxide, hydroxyl, peroxide, drugs (acetaminophen)  
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Superoxide dismutase   neutralizes superoxide  
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Glutathione   neutralizes peroxide, drug FRs  
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Catalase   neutralizes peroxide  
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Lipofuscin   indigestible lipid of lipid peroxidation; brown pigment increased in atrophy and FR damage  
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Reperfusion injury in heart   superoxide FRs + calcium  
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Mitochondrial injury   cytochrome c in cytosol initiates apoptosis  
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SER hyperplasia   alcohol, barbiturates, phenytoin  
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Complications SER hyperplasia   increases drug metabolism (e.g., oral contraceptives); low vitamin D  
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Chediak-Higashi   membrane protein defect in transferring lysosomal enzymes to phagocytic vacuoles  
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Chediak-Higashi   AR; giant lysosomes  
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I cell disease   absent enzyme marker in Golgi apparatus (mannose 6-phosphate); empty lysosomes  
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Rigor mortis   stiff muscles after death due to ATP depletion  
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Fatty change in liver   MCC alcohol (increase in NADH); DHAP → G3P → TG  
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Fatty change in liver   VLDL pushes nucleus to side  
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Causes fatty change   ↑ synthesis TG/FAs, beta-oxidation of FAs, synthesis apoproteins/release VLDL  
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Fatty change in kwashiorkor   ↓ synthesis of apoproteins  
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Ferritin   primary iron storage protein; soluble in blood; serum level reflects marrow storage iron  
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Hemosiderin   insoluble ferritin degradation product visible with Prussian blue stain  
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Atrophy   reduction in cell/tissue mass by either loss or cell shrinkage  
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Brain atrophy   ischemia; Alzheimer's  
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Exocrine gland atrophy in CF   duct obstruction by thick secretions  
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Labile cells   stem cells (skin, marrow, GI tract) →←→⇦  
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Stable cells   in G0 phase (smooth muscle, hepatocytes); can enter cell cycle (growth factors, hormones)  
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Permanent cells   cannot replicate; cardiac/striated muscle; neurons  
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Hypertrophy   increase in cell size (structural components, DNA)  
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LVH   increased preload (valve regurgitation), increased afterload (hypertension, aortic stenosis)  
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RVH   pulmonary hypertension  
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Bladder smooth muscle hypertrophy   prostate hyperplasia constricts urethra  
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Removal of kidney   hypertrophy of remaining kidney  
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Hyperplasia   increase in number of cells  
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Endometrial hyperplasia   unopposed estrogen (obesity, taking estrogen)  
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RBC hyperplasia   increased EPO (blood loss, ectopic secretion, high altitude)  
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Prostate hyperplasia   increased dihydrotestosterone (DHEA)  
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Gynecomastia   hyperplasia male breast tissue; normal in newborn, adolescent, elderly  
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Metaplasia   one adult cell type replaces another cell type  
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Squamous metaplasia in bronchus   smoking  
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Intestinal metaplasia in stomach   Paneth cells, goblet cells; H pylori chronic atrophic gastritis  
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Squamous metaplasia bladder   Schistosoma hematobium infection  
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Barrett's esophagus   glandular metaplasia of distal esophagus; due to GERD  
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Dysplasia   atypical hyperplasia and metaplasia are precursors for cancer  
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Squamous dysplasia in cervix   human papilloma virus  
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Squamous dysplasia in bronchus   smoking  
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Necrosis   death of groups of cells  
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Coagulation necrosis   preservation of structural outline (due to ↑ lactic acid)  
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Infarction   pale (e.g., heart, kidney); hemorrhagic (e.g., lung, small bowel); dry gangrene  
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Liquefactive necrosis   brain infarct, bacterial infections; wet gangrene  
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Caseous necrosis   variant coagulation necrosis; granulomas due to TB/systemic fungi  
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Granulomas   activated macrophages (epithelioid cells); multinucleated giant cells; CD4 TH1 cells  
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Epithelioid cells   γ-interferon released by CD4 T cells activates macrophages  
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Multinucleated giant cells   fusion of epithelioid cells  
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Granulomas   type IV hypersensitivity  
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Enzymatic fat necrosis   associated with pancreatitis; soap formation (Ca2+ + fatty acids)  
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Fibrinoid necrosis   necrosis of immune reactions (immune vasculitis/endocarditis)  
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Postmortem necrosis   autolysis; no inflammatory reaction  
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Dystrophic calcification   calcification of damaged tissue; normal serum calcium  
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Dystrophic calcification   pancreatitis; atherosclerotic plaque  
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Metastatic calcification   calcification of normal tissue; increased serum calcium or phosphorus  
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Nephrocalcinosis   metastatic calcification of collecting tubule basement membranes  
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S/S nephrocalcinosis   polyuria due to nephrogenic diabetes insipidus; renal failure  
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Apoptosis   gene regulated individual cell death  
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Signals activating apoptosis   mullerian inhibitory factor, tumor necrosis factor, hormone withdrawal  
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Signal modulators of apoptosis   TP53 suppressor gene, BCL-2 genes  
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BCL-2 genes   anti-apoptosis gene; prevents cytochrome c from leaving mitochondria  
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Caspases   responsible for enzymatic cell death in apoptosis; proteases and endonucleases  
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Markers of apoptosis   eosinophilic cytoplasm, pyknotic (ink dot) nucleus  
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Apoptosis   loss Mullerian epithelium in male fetus; thymus involution; killing cancer cells  
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Histamine   key chemical in acute inflammation; mast cell; arteriole vasodilation; ↑ venular permeability  
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Rubor acute inflammation   redness; arteriole vasodilation (histamine)  
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Calor acute inflammation   heat; arteriole vasodilation (histamine)  
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Tumor acute inflammation   swelling; ↑ vessel permeability (histamine)  
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Dolor acute inflammation   pain; bradykinin, PGE  
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Acute inflammation   neutrophil dominant; ↑ IgM  
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Initial vessel events   transient vasoconstriction → arteriolar vasodilation → ↑ venular permeability  
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Neutrophil rolling acute inflammation   due to selectins  
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Integrins   neutrophil adhesion molecules; C5a and leukotriene B, activate; neutrophil margination  
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CD11/CD18   markers for integrins  
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Endothelial cell adhesion molecules   activated by IL-1 and TNF  
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ICAM   intercellular adhesion molecule  
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VCAM   vascular cell adhesion molecule Leukocyte adhesion molecule defect  
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Activation neutrophil adhesion molecules   neutrophilic leukocytosis; corticosteroids  
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Activation neutrophil adhesion molecules   neutropenia; endotoxins  
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Chemotaxis   directed movement; C5a and LTB4  
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Opsonizing agents   IgG, C3b; enhance phagocytosis  
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Neutrophils, monocytes, macrophages   receptors for IgG, C3b  
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O2-dependent MPO system   most potent microbicidal system; neutrophils, monocytes  
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ProductionofsuperoxidefromO2   NADPH oxidase with NADPH cofactor; produces respiratory burst  
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Nitro blue tetrazolium (NBT)   test for respiratory burst  
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Superoxide dismutase   converts superoxide to peroxide  
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Myeloperoxidase   lysosomal enzyme that combines peroxide + Cl to form bleach (HOCl)  
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Microbicidal defects   chronic granulomatous disease childhood (XR), myeloperoxidase deficiency (AR)  
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Chronic granulomatous disease   absent NADPH oxidase; no respiratory burst  
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Chronic granulomatous disease   Staphylococcus aureus not killed (catalase positive)  
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Chronic granulomatous disease   Streptococcus killed (catalase negative)  
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Myeloperoxidase deficiency   AR; respiratory burst present; no bleach produced  
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Opsonization defect   Bruton's agammaglobulinemia (XR, decreased IgG)  
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Phagocytosis defect   Chediak-Higashi (see cell injury); also has defect in microtubule polymerization  
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COX inhibitors   non-steroidals (non-selective), selective COX-2 inhibitors  
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PGE2   vasodilation, fever  
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PGI2   vasodilator; prevent platelet aggregation  
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Nitric oxide   vasodilator; FR gas from conversion arginine to citrulline  
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IL-1 and TNF   fever, synthesis acute phase reactants in liver, leukocytosis  
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IL-6   stimulated by IL-1; stimulates synthesis of acute phase reactants  
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Acute phase reactants   fibrinogen, ferritin, C-reactive protein  
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Bradykinin   kinin produced in conversion of factor XII to factor XI  
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Bradykinin   pain, vasodilator, vessel permeability; cough/angioedema, ACE inhibitors  
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Anaphylatoxins   C3a and C5a; directly stimulate mast cell release of histamine  
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Prostaglandin I2   synthesized by endothelial cells; vasodilator, inhibits platelet aggregation  
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Lipoxygenase   hydroxylation of arachidonic acid  
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Zileuton   inhibits lipoxygenase  
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Zafirlukast, montelukast   block lipoxygenase receptor  
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LTC4, -D4, -E4   bronchoconstrictors  
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TXA2   synthesized by platelets; platelet aggregation, vasoconstriction, bronchoconstriction  
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Dipyridamole   inhibits thromboxane synthase  
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Corticosteroids   inhibits phospholipase A2, activation neutrophil adhesion molecules  
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Corticosteroids   neutrophilic leukocytosis, lymphopenia, eosinopenia  
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Fever   right shift OBC; hostile to bacterial/viral replication  
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Chronic inflammation   monocyte/macrophage; ↑ IgG; repair by fibrosis  
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Granuloma   cellular immunity; macrophages interact with TH1 class cells (memory cells)  
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Positive PPD   Langerhan's cells process PPD and interact with TH1 class cells  
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Suppurative inflammation   abscess; Staphylococcus aureus (coagulase)  
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Cellulitis   subcutaneous inflammation; Streptococcus pyogenes (hyaluronidase)  
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Pseudomembranous inflammation   toxins from Corynebacterium diphtheriae, Clostridium difficile  
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Cell cycle   key checkpoint G1 to S phase  
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TP53 and RB suppressor genes   arrests cell in G1 phase for DNA repair or apoptosis  
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BAX gene   stimulates apoptosis; activated by TP53 suppressor gene if too much DNA damage  
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Extracellular matrix   basement membrane, interstitial matrix  
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Complete restoration   cell must be capable of duplication, no damage to basement membrane  
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Scar tissue   end-product of repair by connective tissue  
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Collagen   triple helix of cross-linked α chains  
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Collagen   cross-links at points of hydroxylation (lysyl oxidase) increase tensile strength  
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Type I collagen   bones, tendons  
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Type II collagen   early wound repair  
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Type IV collagen   basement membrane  
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Type X collagen   epiphyseal plate  
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Laminin   key basement membrane glycoprotein  
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Fibronectin   key interstitial matrix glycoprotein  
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Angiogenesis in repair   basic fibroblast growth factor, vascular endothelial growth factor  
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Key event in wound repair   granulation tissue formation; fibronectin responsible  
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Granulation tissue   becomes scar tissue  
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Collagenases   zinc cofactor (metalloprotease); type III collagen replaced by type I collagen  
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Tensile strength of healed wound   80% original strength  
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Inhibition wound healing   infection (MCC S. aureus), zinc deficiency, DM  
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Ehlers-Danlos syndrome   defects in collagen synthesis and structure; hyperelasticity  
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Scurvy   ↓ collagen tensile strength by decreasing cross-links at points of hydroxylation  
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Keloid   excessive type III collagen; common in blacks  
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Pyogenic granuloma   exuberant granulation tissue; bleeds when touched  
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Healing by primary intention   clean wound; appose wound margins with suture  
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Healing by secondary intention   infected wound; leave wound open; myofibroblasts important  
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Liver injury   regenerative nodules; abnormal cytoarchitecture  
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Lung injury   type II pneumocyte repair cell  
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CNS injury   astrocyte and microglial cell repair cells; gliosis  
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WBC alterations in acute inflammation   neutrophilic leukocytosis, left shift, toxic granulation  
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Erythrocyte sedimentation rate   increased fibrinogen enhances rouleaux  
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C-reactive protein   indicator of acute inflammation and inflammatory atheromatous plaque  
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Polyclonal gammopathy   diffuse ↑ of γ-globulins; ↑ IgG; chronic inflammation  
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Total body water   ECF (plasma, interstitial fluid) + ICF (cytosol)  
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Osmosis   H20 shift between ECF and ICF; controlled by serum Na+ and glucose  
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Edema   increased fluid in interstitial space or body cavities; transudate, exudate, lymph  
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Transudate   protein and cell-poor fluid in interstitial space/body cavity; alteration Starling's forces  
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Starling's forces   oncotic pressure (albumin) keeps fluid in vessels, hydrostatic pressure pushes fluid out  
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Pitting edema   decreased oncotic pressure and/or increased hydrostatic pressure  
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↑ Hydrostatic pressure   pulmonary edema in LHF; pitting edema of legs in RHF; portal hypertension  
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Renal retention sodium and water   ↑ hydrostatic pressure and ↓ oncotic pressure  
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Causes of renal retention of sodium/water   ↓ cardiac output (activation RAA system), primary renal disease  
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↓ Oncotic pressure (hypoalbuminemia)   kwashiorkor; nephrotic syndrome; cirrhosis  
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Ascites in cirrhosis   ↓ oncotic pressure, ↑ hydrostatic pressure  
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Exudate   protein and cell rich (pus); acute inflammation with ↑ vessel permeability  
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Lymphedema   radical mastectomy; filariasis; inflammatory carcinoma (lymphatics plugged by tumor)  
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Thrombus   endothelial injury, stasis, hypercoagulability  
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Venous thrombus   fibrin clot with entrapped RBCs, WBCs, platelets; deep veins below knee (stasis)  
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Heparin/warfarin   anticoagulants that prevent venous clot formation  
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Arterial thrombus   endothelial injury; platelets held together by fibrin  
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Aspirin   prevents platelet thrombus in arteries  
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Pulmonary thromboembolism   femoral vein site of origin  
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Systemic thromboembolism   majority from left heart  
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Fat embolus   long bone fractures; delayed symptoms (48 hrs); thrombocytopenia, hypoxemia  
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Amniotic fluid embolism   DIC; lanugo hair in maternal pulmonary arteries  
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Diving   1 atmosphere pressure increase with 33 foot descent into water; N2 gas dissolved in tissue  
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Decompression sickness   release of N2 gas from tissue with rapid ascent; ischemic damage  
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Dyspnea, chest pain underwater   pulmonary embolus  
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Dyspnea, chest pain rising to surface   spontaneous pneumothorax  
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Hypovolemic shock (blood loss)   ↓ CO and LVEDP; ↑ PVR  
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Cardiogenic shock   ↓ CO; ↑ LVEDP and PVR  
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Septic shock   ↑ CO (↑ venous return); ↓ PVR (vasodilation)  
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Kidneys   most susceptible organ in shock; straight portion proximal tubule most susceptible  
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Shock complications   ischemic ATN, multiorgan failure, ↑ AG metabolic acidosis  
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Tumors   parenchyma neoplastic component  
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Benign tumors   epithelial (e.g., adenoma) or connective tissue (e.g., lipoma, leiomyoma)  
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Carcinoma   epithelial origin; squamous cell carcinoma, adenocarcinoma, transitional cell carcinoma  
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Basal cell carcinoma   invades but does not metastasize  
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Squamous cell carcinoma   lower lip, oral pharynx, larynx, lung, esophagus, skin, cervix  
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Adenocarcinoma   distal esophagus → colon, kidney, liver, pancreas, prostate, breast, lung, endometrium  
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Transitional cell carcinoma   renal pelvis, ureter, bladder  
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Sarcoma   malignancy of connective tissue origin; e.g., osteogenic sarcoma (bone)  
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Liposarcoma   MC sarcoma in adults  
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Embryonal rhabdomyosarcoma   MC sarcoma in children  
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Teratoma   ectoderm, endoderm, mesoderm derivatives; bone/teeth visible on x-ray  
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Hamartoma   normal tissue, normal site; bronchial hamartoma, Peutz Jeghers polyp  
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Choristoma   normal tissue aberrant tissue location; pancreatic tissue stomach wall  
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Mixed tumor   different morphologic patterns, same germ cell layer; pleomorphic adenoma parotid  
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Leukemia   malignancy of stem cells in bone marrow  
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Lymphoma   malignancy of lymph nodes  
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Extranodal lymphoma sites   stomach (MC), Peyer's patches  
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Malignant tumors   invade and metastasize; benign tumors do not  
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Upregulate telomerase   increases telomere length; found in all neoplastic cells  
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Monoclonality   key finding in neoplastic vs. normal cells  
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E-Cadherin   intercellular adhesion; lose adhesion in malignant cells  
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Malignant cells   receptors for laminin (basement membrane), fibronectin (ECM)  
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Invasion enzyme   type IV collagenase (basement membrane)  
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Angiogenesis   basic fibroblast growth factor, vascular endothelium growth factor  
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Metastasis   lymphatic, hematogenous, seeding; often more common than primary cancer  
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Carcinoma   lymph node -> hematogenous  
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Vessel invading carcinomas   renal cell carcinoma (renal vein, vena cava), hepatocellular carcinoma  
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Sarcoma   hematogenous  
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Seeding   ovarian cancer, periphery lung, CNS via spinal fluid  
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Sites where metastasis more common primary cancer   lung, bone, brain, liver, adrenal  
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Sites where primary cancer more common than metastasis   GI tract, kidney, urogenital  
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Bone metastasis   osteoblastic (radiodense); osteolytic (radiolucent)  
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Bone sites metastasis   vertebra MC (Batson venous plexus)  
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Osteoblastic metastasis   prostate cancer; increased serum AP, hypercalcemia  
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Osteolytic metastasis   breast cancer  
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EM neurosecretory granules   carcinoid tumors, small cell carcinoma, neuroblastoma  
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EM thin and thick myofilaments   rhabdomyosarcoma  
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EM Birbeck granules   histocytic neoplasms (Langerhan's histiocytosis)  
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Primary prevention   stop smoking; sun screen; high fiber diet  
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Cancers in children   leukemia (MC), CNS tumors, Burkitt's, Ewing's, neuroblastoma  
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Cancer vaccine   hepatitis B vaccine; prevents hepatocellular carcinoma  
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Cancer incidence men   prostate → lung → colorectal  
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Cancer incidence women   breast → lung → colorectal  
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Cancer mortality men   lung → prostate → colorectal  
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Cancer mortality women   lung → breast → colorectal  
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Gynecologic cancers   endometrium → ovary → cervix  
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Cervical Pap smear   decreased incidence of cervical cancer; detects cervical dysplasia  
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Malignant melanoma   fastest increasing in world  
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Southeast China   nasopharyngeal carcinoma (EBV)  
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Southeast Asia   hepatocellular carcinoma (HBV + aflatoxin)  
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Japan   stomach cancer  
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Africa   Burkitt's lymphoma, Kaposi sarcoma (HHV-8)  
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Squamous dysplasia oropharynx, larynx, bronchus, cervix   risk for squamous cell carcinoma (SCC)  
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Chronic irritation sinus orifices, third degree burn scars   risk for SCC  
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Actinic (solar) keratosis   risk factor for SCC  
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Glandular metaplasia of esophagus (Barrett's)   risk factor for adenocarcinoma  
🗑
Endometrial hyperplasia   risk factor for adenocarcinoma  
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Glandular (intestinal) metaplasia of stomach (Helicobacter)   risk factor for adenocarcinoma  
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Chronic ulcerative colitis   risk factor for adenocarcinoma  
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Villous adenoma of rectum   risk factor for adenocarcinoma  
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Tubular adenoma of colon   risk factor for adenocarcinoma  
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Scar tissue in lung   risk factor for adenocarcinoma  
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Regenerative nodules in cirrhosis   risk factor for hepatocellular carcinoma  
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Complete hydatidiform mole   risk factor for choriocarcinoma  
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Dysplastic mole   MC risk factor for malignant melanoma  
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UVB light   MC risk factor for BCC, SCC, melanoma  
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HHV-8   MC risk factor for Kaposi's sarcoma  
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EBV   MC risk factor for nasopharyngeal carcinoma  
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Polycyclic hydrocarbons   MC risk factor for larynx (SCC), lung cancers  
🗑
Asbestos   MC risk factor for mesothelioma  
🗑
Polycyclic hydrocarbons   MC risk factor for oral cavity, mid-esophagus SCC  
🗑
Barrett's esophagus   MC risk factor for distal esophagus adenocarcinoma  
🗑
H. pylori   MC risk factor for stomach adenocarcinoma and lymphoma  
🗑
Tubular adenoma, villous adenoma   MC risk factors for colon adenocarcinoma  
🗑
HBV and HCV   MC risk factors for hepatocellular carcinoma  
🗑
Vinyl chloride   MC risk factor for liver angiosarcoma  
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Gallstones, porcelain gallbladder   MC risk factor for gallbladder adenocarcinoma  
🗑
Polycyclic hydrocarbons   MC risk factor for pancreas adenocarcinoma  
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Polycyclic hydrocarbons   MC risk factor for renal cell carcinoma  
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Polycyclic hydrocarbons   MC risk factor for urinary bladder  
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HPV + lack of circumcision   MC risk factor for penis SCC  
🗑
Age   MC risk factor for prostate adenocarcinoma  
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Cryptorchid testis   MC risk factor for seminoma  
🗑
Age >50 with excess estrogen exposure   MC risk factor for breast and endometrial carcinoma  
🗑
HPV 16/18   MC risk factor for vulva, vagina, cervix SCC  
🗑
DES   MC risk factor for vagina/cervix clear cell carcinoma  
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Nulliparity   MC risk factor for surface derived ovarian cancer  
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Complete mole   MC risk factor for choriocarcinoma  
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Turner syndrome (XO)   MC risk factor for dysgerminoma of ovary  
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Turner syndrome (XO/XY)   gonadoblastoma of ovary  
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Ionizing radiation   MC risk factor for papillary cancer of thyroid  
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Family history (MEN IIa/IIb)   MC risk factor for medullary carcinoma thyroid  
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Hashimoto's thyroiditis   MC risk factor for malignant lymphoma thyroid  
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Ionizing radiation   MC risk factor for osteogenic sarcoma  
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EBV   MC risk factor for primary CNS lymphoma in AIDS and Burkitt's lymphoma  
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Ionizing radiation   MC risk factor for acute/chronic myelogenous leukemia  
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EBV   MC risk factor for Burkitt's lymphoma  
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HTLV-1   MC risk factor for T cell leukemia/lymphoma  
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Bacterial causes of cancer   H. pylori (stomach adenocarcinoma and lymphoma)  
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Parasitic causes of cancer   S. hematobium (SCC bladder), C. sinensis (cholangiocarcinoma)  
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Carcinogenesis   mutations involving regulatory genes  
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Regulatory genes   proto-oncogenes, suppressor genes, anti-apoptosis genes  
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Types mutations   point mutation MC, translocation, amplification (↑ copies), overexpression (↑ activity)  
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Translocations   Burkitt's t(8;14); CML t(9;22); follicular lymphoma t(14;18); APL leukemia t(15;17)  
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Key cancer genes   TP53 suppressor gene, RAS protooncogene  
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Point mutation   inactivates suppressor genes (e.g., TP53), activates proto-oncogenes (e.g., RAS)  
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Amplification   activates ERB-B2  
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Overexpression   enhances activity of BCL-2  
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S/S POC   function-growth factor synthesis; mutation-overexpression  
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ERB-B2 POC   function growth factor receptor; activation bad prognostic sign for breast carcinoma  
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RAS POC   function-GTP signal transduction; point mutation; 30% of all human cancer  
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ABL POC   function-non-receptor tyrosine kinase activity; translocation (9;22) causing CML  
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MYC POC   function nuclear transcription; translocation (8; 14) causing Burkitt's lymphoma  
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Inactivation suppressor genes   majority are point mutations; loss of suppression  
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Sporadic retinoblastoma   two hit theory; two separate point mutations of RB suppressor gene on  
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AD retinoblastoma   one hit theory; one already inactivated in germ cells  
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TP53 suppressor gene functions   G,-S phase inhibition, DNA repair, activation BAX apoptosis gene  
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Inactivation TP 53 suppressor gene   inactivation causes majority of human cancers  
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RB suppressor gene function   G1-S phase inhibition  
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Inactivation RB suppressor gene   retinoblastoma, osteogenic sarcoma  
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APC suppressor gene function   prevents nuclear transcription by catenin  
🗑
Inactivation APC suppressor gene   familial polyposis (FAP)  
🗑
BRCA1/2 suppressor genes function   DNA repair inactivation  
🗑
BRCA 1/2 suppressor genes   breast, ovarian cancers  
🗑
BCL-2 function   anti apoptosis gene (keeps cytochrome c in mitochondria)  
🗑
BCL-2 gene   t(14;18) translocation of heavy chain causes overexpression; follicular B cell lymphoma [think t(14;18) = t(l4;lB) for foLLicular B]  
🗑
Xeroderma pigmentosum   AR; defect in DNA repair enzymes; ↑ risk for UVB light cancers  
🗑
Hereditary non-polyposis syndrome (HNPCC)   AD; inactivation DNA mismatch genes; colorectal cancer  
🗑
Chromosome instability syndromes   AR; susceptibility to DNA damage; leukemias, lymphomas  
🗑
Examples chromosome instability   Bloom syndrome, ataxia telangiectasia, Wiskott-Aldrich syndrome  
🗑
Carcinogens   chemicals (MC), viruses, radiation, H. pylori, physical (squamous cancer in bum scar)  
🗑
Polycyclic hydrocarbons   key chemical carcinogen (cigarette smoke)  
🗑
Aflatoxins   produced from Aspergillus; hepatocellular carcinoma  
🗑
Asbestos   lung cancer, mesothelioma  
🗑
Thorium dioxide   hepatocellular carcinoma, cholangiocarcinoma  
🗑
Aniline dyes   transitional cell carcinoma  
🗑
Vinyl chloride   angiosarcoma of liver  
🗑
Benzene   leukemia  
🗑
Cyclophosphamide   transitional cell carcinoma of bladder  
🗑
EBV   Burkitt's; CNS lymphoma (AIDS); Hodgkin's mixed cellularity; nasopharyngeal carcinoma  
🗑
HBV and HCV   hepatocellular carcinoma  
🗑
HPV   cervical, penis, and anorectal squamous cancers  
🗑
HHV-8   Kaposi sarcoma  
🗑
UVB cancers   basal cell carcinoma, squamous cell carcinoma, malignant melanoma  
🗑
Key host defense   cytotoxic CD8 T cells (type IV hypersensitivity)  
🗑
Cachexia   due to tumor necrosis factor-α  
🗑
Most common anemia   anemia chronic disease  
🗑
Most common coagulopathy   hypercoagulability  
🗑
Most common COD in cancer   gram negative infection  
🗑
Clubbing   possible marker for lung cancer  
🗑
Non-bacterial thrombotic endocarditis mitral valve   possible marker for pancreatic cancer  
🗑
TNM staging   metastasis more important than nodal involvement  
🗑
AFP   hepatocellular carcinoma, yolk sac tumors  
🗑
PSA   prostate cancer  
🗑
CEA   recurrence colorectal cancer  
🗑
BJ (Bence-Jones) protein   multiple myeloma  
🗑
β-human chorionic gonadotropin   choriocarcinoma  
🗑
Calcitonin   medullary carcinoma thyroid; hypocalcemia  
🗑
Small cell carcinoma lung   ADH (hyponatremia), ACTH (ectopic Cushing's)  
🗑
Renal cell carcinoma   EPO (polycythemia), PTH-related peptide (hypercalcemia)  
🗑
Hepatocellular carcinoma   EPO (polycythemia), insulin-like factor (hypoglycemia)  
🗑
Medullary carcinoma of thyroid   calcitonin (hypocalcemia), ACTH (ectopic Cushing's)  
🗑
Squamous cell carcinoma of lung   PTH-related peptide (hypercalcemia)  
🗑
Erythropoietin   synthesized in peritubular capillaries  
🗑
Reticulocyte count   measure of effective erythropoiesis; correct for degree of anemia  
🗑
Extramedullary hematopoiesis   hematopoiesis outside bone marrow (e.g., spleen)  
🗑
Newborn physiologic anemia   drop in Hb due to replacement of HbF RBCs with HbA  
🗑
Pregnancy   Hb and Hct decreased; greater increase in plasma volume than RBC mass  
🗑
Anemia   normal O2 saturation and arterial PO2  
🗑
MCV   average volume of RBCs; useful for anemia classification  
🗑
MCHC   average Hb concentration in RBCs  
🗑
MCHC   ↓ in microcytic anemias; ↑ in spherocytosis  
🗑
Thalassemias   ↓ MCV, ↑ RBC count  
🗑
RDW   RBC size variation; ↑ iron deficiency; normal in other microcytic anemias  
🗑
Mature RBC   anaerobic glycolysis; no mitochondria or HLA antigens  
🗑
Total iron binding capacity   ↑ iron deficiency; ↓ anemia chronic disease, sideroblastic anemia  
🗑
% Saturation   ↓ iron deficiency, anemia chronic disease; ↑ sideroblastic anemia  
🗑
Serum ferritin   ↓ iron deficiency; ↑ anemia chronic disease, sideroblastic anemia; normal thalassemia  
🗑
Microcytic anemias   iron deficiency MC, anemic chronic disease, thalassemia, sideroblastic anemia  
🗑
Iron deficiency child   MCC Meckel's diverticulum  
🗑
Iron deficiency woman < 50   MCC menorrhagia  
🗑
Iron deficiency man < 50   MCC peptic ulcer disease  
🗑
Iron deficiency men/woman > 50   MCC colon cancer  
🗑
Stages iron deficiency   ↓ ferritin; ↓ Fe and % saturation, ↑ TIBC; normocytic then microcytic anemia  
🗑
Anemia chronic disease   MC anemia in malignancy and alcoholics  
🗑
α-Thalassemia trait   AR; two α-globin gene deletions; normal Hb electrophoresis  
🗑
HbH disease   three α-globin gene deletions; hemolytic anemia; four β-globin chains  
🗑
Hb Bart's disease   four α-globin gene deletions; four γ-globin chains  
🗑
β-Thalassemia minor   AR; DNA splicing defect; ↑ HbA2 and F; ↓ HbA  
🗑
β-Thalassemia major   nonsense mutation with stop codon; hemolytic anemia; ↑↑ HbF, ↑ HbA2  
🗑
Sideroblastic anemia   defect in mitochondrial heme synthesis producing ringed sideroblasts  
🗑
Causes sideroblastic anemia   alcohol, pyridoxine deficiency (isoniazid Rx of TB), Pb poisoning  
🗑
Pb poisoning   inhibition ferrochelatase, d-aminolevulinic acid dehydrase, ribonuclease  
🗑
S/S Pb poisoning children   growth retardation; Pb in epiphyses (lead lines); abdominal colic; encephalopathy  
🗑
S/S Pb poisoning adult   peripheral neuropathy; proximal renal tubule damage (Fanconi's syndrome)  
🗑
Lab Pb poisoning   coarse basophilic stippling RBCs; ↓ MCV; ↑ blood Pb; ↑ d-aminolevulinic acid  
🗑
Vitamin B12   animal products; requires intrinsic factor for reabsorption in terminal ileum  
🗑
Vitamin B12   transfers methyl group to homocysteine  
🗑
R factor   binds with B12 in mouth, removed by pancreatic enzymes in small intestine  
🗑
Vitamin B12   involved in propionate metabolism; end-product succinyl CoA  
🗑
Causes B12 deficiency   vegan, pernicious anemia MC, fish tapeworm, pancreatitis, bacterial overgrowth, Crohn's disease  
🗑
Pernicious anemia   autoimmune destruction parietal cells; chronic gastritis body/fundus; achlorhydria; ↑ gastrin  
🗑
Causes folate deficiency   alcohol MCC, poor diet, drugs, malabsorption, pregnancy, goat milk  
🗑
Drugs and folate deficiency   alcohol, OC, phenytoin, methotrexate, trimethoprim, 5-fluorouracil  
🗑
Intestinal conjugase in folate metabolism   inhibited by phenytoin  
🗑
Jejunal uptake of monoglutamate form of folate   inhibited by alcohol and OC  
🗑
Dihydrofolate reductase   inhibited by methotrexate, trimethoprim  
🗑
Thymidylate synthetase   inhibited by 5-fluorouracil  
🗑
Folate deficiency   MCC of increased serum homocysteine  
🗑
Lab in B12/folate deficiency   pancytopenia; hypersegmented neutrophils; ↑ homocysteine  
🗑
Lab findings unique to B12 deficiency   ↑ gastrin (pernicious anemia), ↑ methylmalonic acid  
🗑
B12 reabsorbed absorbed after administration of intrinsic factor   PA  
🗑
B12 reabsorbed absorbed after administration of antibiotics   bacterial overgrowth  
🗑
B12 reabsorbed absorbed after administration of pancreatic extract   chronic pancreatitis  
🗑
Acute blood loss   initially normal Hb and Hct; 0.9% saline uncovers RBC deficit  
🗑
Aplastic anemia   drugs (e.g., phenylbutazone); infection (e.g., parvovirus); benzene  
🗑
Lab findings aplastic anemia   pancytopenia; hypocellular bone marrow  
🗑
Anemia in renal disease   normocytic; decreased EPO  
🗑
Extravascular hemolysis   macrophage phagocytosis of RBCs; ↑ unconjugated bilirubin and urine UBG  
🗑
Intravascular hemolysis   ↓ serum haptoglobin; hemoglobinuria; hemosiderinuria  
🗑
Congenital spherocytosis   AD; defect in spectrin; extravascular hemolysis; splenomegaly  
🗑
Blood findings in spherocytosis   normocytic anemia; dense RBCs, ↑ MCHC, ↑ osmotic fragility  
🗑
PNH   missing decay accelerating factor; complement destruction RBCs, neutrophils, platelets  
🗑
S/S PNH   pancytopenia; hemoglobinuria; positive sugar water (Ham's) test and acidified serum test  
🗑
HbSS   AR; missense mutation (valine for glutamic acid 6th positive β-globin chain)  
🗑
Causes of sickling   ↑ deoxyhemoglobin (hypoxemia, acidosis); HbS > 60%  
🗑
HbF   inhibits sickling; hydroxyurea ↑ HbF  
🗑
Pathophysiology HbSS   vasoocclusive crises, hemolytic anemia (extravascular)  
🗑
HbSS children   dactylitis (6-9 months); Streptococcus pneumoniae sepsis (dysfunctional spleen)  
🗑
HbSS osteomyelitis   Salmonella paratyphi  
🗑
HbSS complications   aplastic crisis (parvovirus B-19), acute chest syndrome, autosplenectomy, calcium bilirubinate gallstones, priapism, aseptic necrosis  
🗑
HbAS   microhematuria from sickling in renal medulla; renal papillary necrosis  
🗑
Hb electrophoresis   HbAS-HbA 55-60%, HbS 40-45%; HbSS-HbS 90-95%, HbF 5-10%  
🗑
Blood findings in HbSS   sickle cells; target cells; Howell-Jolly bodies (nuclear remnants)  
🗑
G6PD deficiency   XR; oxidant damage (peroxide) to Hb (e.g., primaquine; dapsone; fava beans)  
🗑
Blood findings G6PD deficiency   Heinz bodies (denatured Hb; special stain); bite cells  
🗑
Pyruvate kinase deficiency   ↓ ATP; RBCs dehydrated; ↑ 2,3-BPG (right-shifted OBC)  
🗑
Warm type AIHA   IgG; extravascular hemolysis; e.g., SLE, drugs  
🗑
Cold type AIHA   IgM intravascular hemolysis; e.g., CLL, Mycoplasma  
🗑
Penicillin   IgG antibody against penicillin attached to RBC (type II hypersensitivity)  
🗑
Methyldopa   drug alters Rh antigens; IgG antibody against Rh antigens (type II hypersensitivity)  
🗑
Quinidine   drug-IgM IC; intravascular hemolysis; type III hypersensitivity  
🗑
Lab findings AIHA   positive direct Coombs'; spherocytes  
🗑
Micro-macroangiopathic hemolysis   mechanical damage causing intravascular hemolysis  
🗑
Causes of micro/macro hemolysis   aortic stenosis (MCC), DIC, TIP, HUS  
🗑
Peripheral blood findings micro/macro hemolysis   schistocytes; iron deficiency from hemoglobinuria  
🗑
Malaria   intravascular hemolysis correlates with fever; falciparum-ring forms and gametocytes  
🗑
Leukemoid reaction   exaggerated WBC response to infection; usually due to infection  
🗑
Leukoerythroblastic reaction   marrow infiltrative disease peripheralizes myeloblasts/nucleated RBCs  
🗑
Causes of leukoerythroblastic reaction   bone metastasis MCC, myelofibrosis  
🗑
Eosinophilia   type I hypersensitivity (e.g., penicillin reaction); invasive helminthic infection  
🗑
Helminthes not producing eosinophilia   pinworms, adult worms in ascariasis  
🗑
Atypical lymphocytes   mononucleosis; CMV; toxoplasmosis; viral hepatitis; phenytoin  
🗑
Mononucleosis   due to EBV; EBV attaches to CD21 receptors on B cells  
🗑
Clinical findings mono   exudative tonsillitis, generalized lymphadenopathy, hepatosplenomegaly  
🗑
Lab findings mono   atypical lymphocytosis; IgM heterophile antibodies against horse RBCs  
🗑
Lymphopenia   T cell deficiencies (HIV); combined B/T deficiency (adenine deaminase deficiency)  
🗑
Lymphocytosis   viral infections, whooping cough  
🗑
Corticosteroids   lymphopenia, eosinopenia, neutrophilia  
🗑
Chronic MPD   neoplastic stem cell disorder; splenomegaly; marrow fibrosis; risk for leukemia  
🗑
Examples of MPD   polycythemia vera, myelofibrosis and myeloid metaplasia  
🗑
Relative polycythemia   ↓ plasma volume; ↑ RBC count; normal RBC mass  
🗑
Absolute polycythemia   ↓ RBC count and RBC mass  
🗑
Appropriate polycythemia   hypoxic stimulus for EPO to generate RBCs  
🗑
Causes of appropriate absolute polycythemia   lung disease, cyanotic heart disease, high altitude  
🗑
Appropriate absolute polycythemia   normal plasma volume; ↑ RBC mass; ↓ SaO2; ↑ EPO  
🗑
Inappropriate absolute polycythemia   no hypoxic stimulus for EPO  
🗑
Causes of inappropriate polycythemia   ectopic secretion EPO, polycythemia vera  
🗑
Polycythemia vera   ↑ plasma volume and RBC mass; normal SaO2; ↓ EPO  
🗑
Ectopic EPO (renal cell carcinoma)   normal plasma volume; ↑ RBC mass; normal SaO2; ↑ EPO  
🗑
Myelofibrosis myeloid metaplasia   marrow fibrosis; extramedullary hematopoiesis; splenomegaly  
🗑
Lab findings in myelofibrosis   tear drop RBCs; dry bone marrow aspirate (marrow fibrosis)  
🗑
Essential thrombocythemia   MPO with increase in abnormal appearing platelets  
🗑
Myelodysplastic syndrome   severe anemia in elderly; 30% develop leukemia; ringed sideroblasts  
🗑
Benzene   aplastic anemia; acute leukemia  
🗑
Leukemia by age   ALL, newborn-14; AML, 15-60; CML, 40-60; CLL, >60  
🗑
Acute vs. chronic leukemia   acute, blasts >30% in bone marrow; chronic, blasts <10% in bone marrow  
🗑
AML   Auer rods in myeloblasts  
🗑
Acute promyelocytic leukemia   t(15;17); defect in retinoic acid; Rx retinoic acid (↑ maturation); DIC  
🗑
Acute monocytic leukemia   gum infiltration  
🗑
CML   t(9;22) of ABL POC; Philadelphia chromosome 22; ↓ alkaline phosphatase score  
🗑
ALL   early pre-B (80%); CALLA (CD10) and TdT positive; CNS and testicle involvement  
🗑
ALL   t(12;21) offers good prognosis  
🗑
CLL   B cell neoplasm; ↓ γ-globulins; MCC generalized lymphadenopathy patients> 60-yrs-old  
🗑
Adult T cell leukemia   HTLV-1; CD4 T cells; skin infiltration; lytic bone lesions with hypercalcemia  
🗑
Hairy cell leukemia   positive TRAP stain; splenomegaly; Rx with purine nucleosides; (+)CD11c  
🗑
Nodal sites   germinal follicles, B cells; paracortex, T cells; sinuses, histiocytes  
🗑
Testicular cancer   metastasizes to para-aortic nodes  
🗑
Stomach cancer   metastasizes to left supraclavicular nodes (Virchow node)  
🗑
Phenytoin   atypical lymphocytosis  
🗑
Cat scratch disease   Bartonella henselae; granulomatous microabscesses  
🗑
Follicular B-cell lymphoma   t(14;18); overexpression of BCL-2 anti-apoptosis gene  
🗑
Burkitt lymphoma   t(8;14); EBV association; common childhood NHL; "starry sky" appearance  
🗑
Extra nodal lymphomas   risk factors H. pylori (stomach); Sjogren's syndrome  
🗑
Mycosis fungoides   CD4 T cell neoplasm; skin lesions with Pautrier's microabscesses  
🗑
Sezary syndrome   leukemic phase of mycosis fungoides  
🗑
Polyclonal gammopathy   sign of chronic inflammation  
🗑
Monoclonal gammopathy   M component (spike); sign of plasma cell disorder  
🗑
Confirmatory tests   serum and urine immunoelectrophoresis; bone marrow aspirate  
🗑
Bence Jones protein   light chains in urine; predictive of a malignant plasma cell disorder  
🗑
Multiple myeloma   M spike; lytic bone lesions; pathologic fractures; hypercalcemia; renal failure  
🗑
MGUS   MC monoclonal gammopathy; may progress to myeloma  
🗑
Findings in MGUS   elderly patient; no BJ protein; no malignant plasma cells  
🗑
Waldenstrom's macroglobulinemia   lymphoplasmacytic lymphoma; IgM M spike; hyperviscosity  
🗑
Hodgkin's lymphoma   neoplastic component, Reed Stemberg (RS) cell; CD15 & CD30 positive  
🗑
Lymphocyte predominant Hodgkin's   infrequent classic RS cells  
🗑
Nodular sclerosing Hodgkin's   female dominant; supraclavicular nodes + anterior mediastinal nodes  
🗑
Mixed cellularity Hodgkin's   male dominant; numerous RS cells; EBV association  
🗑
Hodgkin's prognosis   stage of disease and type of Hodgkin's most important factors  
🗑
Alkylating agents in Rx of Hodgkins   ↑ risk for second malignancies (leukemia; NHL)  
🗑
Langerhan's histiocytes   CD1 positive; Birbeck granules  
🗑
Letterer-Siwe disease   malignant histiocytosis <2 yrs old; diffuse eczematous rash; organ involvement  
🗑
Hand-Christian-Christian disease   malignant; lytic skull lesions, diabetes insipidus, exophthalmos  
🗑
Eosinophilic granuloma   benign histiocytosis; lytic bone lesions with pathologic fractures  
🗑
Mast cells   release histamine (pruritus; swelling); metachromatic granules positive with toluidine blue  
🗑
Urticaria pigmentosum   localized mastocytosis; skin lesions swell and itch with scratching  
🗑
Amyloid   twisted β-sheet; apple green birefringence with Congo red  
🗑
Primary amyloidosis   AL amyloid derived from light chains; plasma cell disorders  
🗑
Secondary amyloidosis   AA amyloid derived from serum-associated amyloid; chronic infections  
🗑
Alzheimer's disease   amyloid precursor protein gene product chromosome 21; amyloid-β  
🗑
Gaucher's disease   macrophages have fibrillary appearance; deficiency glucocerebrosidase  
🗑
Niemann Pick's disease   macrophages have soap bubble appearance; deficiency sphingomyelinase  
🗑
Hypersplenism   splenomegaly; peripheral blood cytopenias; portal hypertension MCC  
🗑
Splenic dysfunction   Howell Jolly bodies; susceptible to Streptococcus pneumoniae sepsis  
🗑
Anticoagulants   tissue plasminogen activator, heparin, PGI2 ATIII, protein C/S  
🗑
Heparin   enhances ATIII activity (neutralizes all factors except V, VIII, fibrinogen)  
🗑
Protein C/S   neutralize V and VIII  
🗑
Procoagulants   coagulation factors, thromboxane A2 (platelet aggregation, vasoconstrictor)  
🗑
Protein C and S   inactivate factors V and VIII; enhance fibrinolysis  
🗑
von Willebrand factor   complexes with factor VIII to enhance VIII:C activity; platelet adhesion  
🗑
Platelets   receptors for von Willebrand factor and fibrinogen; synthesize thromboxane A2  
🗑
GpIb   platelet receptor for von Willebrand factor  
🗑
GpIIb:IIIa   platelet receptor for fibrinogen  
🗑
Extrinsic system factor   VII  
🗑
Intrinsic system factors   XII, XI, IX, VIII  
🗑
Final common pathway factors   X, V, prothrombin (II), fibrinogen (I)  
🗑
Factor XIII   cross-links insoluble fibrin; strengthens fibrin clots  
🗑
Vitamin K-dependent factors   prothrombin, VII, IX, X, protein C and S  
🗑
Factors consumed in a clot   fibrinogen, prothrombin, V, VIII; fluid is called serum  
🗑
Plasmin   cleaves fibrinogen and insoluble fibrin into degradation products  
🗑
Bleeding time   evaluates platelet function (adhesion, release reaction, aggregation)  
🗑
Aspirin   MCC of a prolonged bleeding time  
🗑
Tests for vWF   ristocetin cofactor assay; vWF antigen assay; agar electrophoresis  
🗑
PT   evaluates extrinsic pathway to fibrin clot  
🗑
PTT   evaluates intrinsic pathway to stable fibrin clot  
🗑
Fibrinolysis tests   fibrin(ogen) degradation products; D-dimers (cross-linked insoluble fibrin)  
🗑
S/S platelet dysfunction   cannot form temporary plug; epistaxis; petechiae; bleeding from scratches  
🗑
Idiopathic thrombocytopenic purpura (ITP)   children; antibodies against GpIIb:IIIa; no splenomegaly  
🗑
Chronic autoimmune thrombocytopenic purpura   SLE; antibodies against GpIIb:IIIa receptors  
🗑
Heparin   thrombocytopenia due to IgG antibody against heparin attached to PF4 on platelets  
🗑
PF4   heparin neutralizing factor  
🗑
HIV   thrombocytopenia MC hematologic abnormality; similar to ITP  
🗑
TTP   platelet thrombi develop in areas of endothelial damage in small vessels; consumption of platelets  
🗑
S/S   fever, thrombocytopenia, renal failure, hemolytic anemia with schistocytes, CNS deficits  
🗑
Lab findings TTP   thrombocytopenia, prolonged bleeding time, normal PT and PTT  
🗑
HUS   similar to TTP; endothelial injury from Shiga-like toxin of 0157:H7 E. coli in undercooked beef  
🗑
S/S factor deficiency   no stable fibrin clot-late rebleeding; menorrhagia; GI bleeding; hemarthroses  
🗑
Hemophilia A   XR; hemarthroses; prolonged PTT, ↓ factor VIII activity, normal VIII antigen  
🗑
von Willebrand's disease   AD; platelet adhesion defect + factor VIII deficiency  
🗑
Lab findings in VWD   ↓ vWF, VIII antigen, and VIII:C; prolonged bleeding time  
🗑
Desmopressin acetate   Rx of choice for mild von Willebrand's disease and hemophilia A  
🗑
Circulating anticoagulants   antibodies destroy coagulation factors  
🗑
Lab finding in circulating anticoagulant   prolonged PT and/or PTT corrected with mixing studies  
🗑
Vitamin K deficiency   ↓ epoxide reductase activity (↓ function vitamin K); hemorrhagic diathesis; ↑ PT  
🗑
Causes vitamin K deficiency   antibiotics MC, newborn, malabsorption, warfarin  
🗑
DIC   activation coagulation system from release of tissue thromboplastin and/or endothelial cell damage  
🗑
DIC   consumption coagulation factors by fibrin clots; patient also anticoagulated  
🗑
Causes   septic shock MCC, rattlesnake bite, massive trauma, amniotic fluid  
🗑
S/S   bleeding from all scratches, holes, needle sites  
🗑
Lab findings DIC   thrombocytopenia, ↑ PT and PTT, D-dimers (best test), anemia  
🗑
Antiphospholipid antibodies   lupus anticoagulant and anticardiolipin antibodies; vessel thrombosis  
🗑
Warfarin   inhibits epoxide reductase; PT best test but PTT also prolonged  
🗑
Warfarin   full anticoagulation in 3 days when -carboxylated prothrombin disappears  
🗑
Warfarin   ingredient in rat poison; danger to children in households with grandparents on warfarin  
🗑
Rx warfarin over anticoagulation   intramuscular vitamin K (6-8 hrs), fresh frozen plasma (immediate)  
🗑
Heparin   enhances ATIII; PTT best test but PT also prolonged  
🗑
OC   estrogen ↑ coagulation factor synthesis and ATIII; predisposes to thrombosis  
🗑
Factor V Leiden   MC hereditary thrombosis; resistant to degradation by protein C/S  
🗑
ATIII deficiency   no prolongation of PTT with administration of heparin  
🗑
Hemorrhagic skin necrosis   post-warfarin therapy in patient with heterozygote protein C deficiency  
🗑
M cells   specialized cells that transfer foreign antigens to lymphocytes in Peyer's patches  
🗑
Blood group O   some patients have anti-AB-IgG antibodies; increased incidence duodenal ulcers  
🗑
Blood group A   increased incidence of gastric carcinoma  
🗑
Newborns   do not have natural blood group antibodies at birth (e.g., anti-A-lgM)  
🗑
Elderly   may lose natural blood group antibodies; no hemolytic reaction to mismatched blood  
🗑
Rh antigens   inherited in autosomal codominant fashion; Rh antigens include D, C, c, E, e  
🗑
Atypical antibodies   antibodies against Rh or non-Rh blood group antigens (e.g., anti-D)  
🗑
Duffy antigen   receptor for Plasmodium vivax; blacks often lack Duffy antigen  
🗑
Antibody screen   indirect Coomb's test; detects atypical antibodies in serum  
🗑
Cytomegalovirus   MC infection transmitted by blood transfusion; MC antibody  
🗑
Hepatitis C   MCC of post-transfusion hepatitis  
🗑
Major crossmatch   patient serum reacted against donor RBCs; does not guarantee RBC survival  
🗑
Universal donor   blood group O; no antigens on the surface of RBCs  
🗑
Universal recipient   blood group AB; no natural blood group antibodies in serum  
🗑
Packed RBC transfusion   raises Hb by 1 gm/dL and Hct by 3%  
🗑
Cryoprecipitate   fibrinogen and factor VIII  
🗑
Fresh frozen plasma   replacement for multiple factor deficiencies (e.g., cirrhosis, DIC)  
🗑
Allergic transfusion reaction   type I IgE-mediated hypersensitivity reaction  
🗑
Febrile transfusion reaction   recipient anti-HLA antibodies react against donor leukocytes  
🗑
Intravascular HTR   transfusion of ABO incompatible blood (e.g., A person receives B blood)  
🗑
Extravascular HTR   antibody attaches to donor RBCs; macrophage phagocytosis and hemolysis  
🗑
Positive direct Coomb's test   present in both types of hemolytic transfusion reactions  
🗑
S/S   jaundice, no increase in Hb, hemoglobinuria  
🗑
ABO HDN   mother O and baby A or B; transplacental passage of maternal anti-AB-IgG  
🗑
ABO HDN   positive direct Coomb's test; spherocytes; MCC unconjugated hyperbilirubinemia first 24 hrs  
🗑
Rh HDN   mother Rh (D antigen) negative and fetus Rh (O antigen) positive  
🗑
Rh HDN   no hemolysis in first Rh incompatible pregnancy  
🗑
Rh HDN   maternal anti-D crosses placenta; potential for hydrops fetalis; high risk for kernicterus  
🗑
Rh immune globulin   anti-D; coats D antigen site on fetal RBCs in maternal circulation  
🗑
Rh HDN lab   positive direct Coomb's; severe anemia and hyperbilirubinemia  
🗑
ABO HDN   protects mother from Rh sensitization (development of anti-D antibodies)  
🗑
O Rh negative mother with A Rh positive baby   A+ cells destroyed by mothers anti A-lgM  
🗑
Blue fluorescent light   converts unconjugated bilirubin in skin into harmless water soluble dipyrrole  
🗑
MV auscultation   apex  
🗑
TV auscultation   left parasternal border  
🗑
AV auscultation   right 2nd intercostal space  
🗑
PV auscultation   left 2nd intercostal space  
🗑
S1   closure MV and TV  
🗑
S2   closure AV and PV  
🗑
Inspiration   split in A2 and P2; due to increased blood in right side of heart  
🗑
S3   abnormal; due to blood entering volume overloaded ventricle in early diastole  
🗑
Causes S3   valve regurgitation; congestive heart failure  
🗑
S4   abnormal; due to blood entering non-compliant ventricle with atrial contraction in late diastole  
🗑
Causes S4   volume overloaded ventricle, hypertrophy  
🗑
Murmurs   stretching valve ring or damage to valve  
🗑
Inspiration   increases right sided abnormal heart sounds and murmurs  
🗑
Expiration   increases left sided abnormal heart sounds and murmurs  
🗑
Stenosis murmurs   problem in opening valve  
🗑
Regurgitation murmurs   problem in closing valve  
🗑
Valves opening in systole   AV and PV  
🗑
Valves opening in diastole   MV and TV  
🗑
Valves closing in systole   MV and TV  
🗑
Valves closing in diastole   AV and PV  
🗑
LDL   primary vehicle for carrying cholesterol  
🗑
VLDL   primary vehicle for carrying liver-synthesized triglyceride  
🗑
Familial hypercholesterolemia (type II)   AD; deficiency of LDL receptors; ↑ LDL  
🗑
Type III hyperlipoproteinemia   deficiency apo E; ↑ remnants (chylomicron, intermediate density)  
🗑
Type IV hyperlipoproteinemia   ↑ VLDL; alcoholics  
🗑
Apo B deficiency   deficiency apo B48 (chylomicrons) and B100 (VLDL); ↓ CH and TG  
🗑
Clinical findings in apo B deficiency   malabsorption; hemolytic anemia  
🗑
Atherosclerosis   reaction to injury of endothelial cells  
🗑
Risk factors   smoking, ↑ LDL, ↑ homocysteine, Chlamydia pneumoniae infection  
🗑
Cells involved   platelets, macrophages, smooth muscle cells, T cells with cytokine release  
🗑
Fibrous plaque   pathognomonic lesion of atherosclerosis  
🗑
C-reactive protein   marker of an inflammatory atheromatous plaque  
🗑
Inflammatory atheromatous plaque   predisposes to platelet thrombosis  
🗑
Increased plasma homocysteine   ↑ vessel thrombosis; folate (MC)/vitamin B12 deficiency  
🗑
Hyaline arteriolosclerosis   small vessel disease of DM and hypertension; excess protein in vessel wall  
🗑
Mechanisms hyaline arteriolosclerosis in DM   non-enzymatic glycosylation  
🗑
Non-enzymatic glycosylation   glucose attaches to amino acids in BM; causes ↑ permeability to protein  
🗑
Mechanisms hyaline arteriolosclerosis in hypertension   pressure pushes proteins into vessel wall  
🗑
Abdominal aortic aneurysm rupture   due to atherosclerosis; flank pain, hypotension, pulsatile mass  
🗑
Syphilitic aneurysm   vasculitis of vasa vasorum of aortic arch; aortic regurgitation  
🗑
Aortic dissection   due to hypertension and collagen tissue disorders (e.g., Marfan)  
🗑
Cystic medial degeneration   elastic tissue degeneration creates spaces filled with mucopolysaccharides  
🗑
Intimal tear in aorta   due to wall stress from hypertension and structural weakness  
🗑
Types of dissection   proximal (MC); distal or combination of both  
🗑
S/S proximal aortic dissection   chest pain radiating to back, lack of pulse; cardiac tamponade MC COD  
🗑
Marfan's   AD; fibrillin defect; aortic regurgitation/dissection; lens dislocation; MVP with sudden death  
🗑
MC COD Marfan's and Ehlers Danlos   aortic dissection  
🗑
Phlebothrombosis   stasis of blood flow; deep veins below knee MC site  
🗑
Pulmonary thromboembolism   emboli originate from femoral veins  
🗑
Superficial migratory thrombophlebitis   sign of carcinoma of head of pancreas  
🗑
Thoracic outlet syndrome   absent radial pulse with positional change  
🗑
Turner's syndrome   lymphedema hands/feet in newborn; preductal coarctation  
🗑
Spider telangiectasia   arteriovenous fistula; due to hyperestrinism (cirrhosis, pregnancy)  
🗑
Capillary hemangioma in newborn   regress with age; do not surgically remove  
🗑
Kaposi's sarcoma   HHV-8; vascular malignancy; MC cancer in AIDS  
🗑
Bacillary angiomatosis   Bartonella henselae; vascular infection in AIDS  
🗑
Small vessel vasculitis   palpable purpura; e.g., Henoch Schonlein purpura  
🗑
Muscular artery vasculitis   vessel thrombosis with infarction; e.g., classical polyarteritis nodosa  
🗑
Elastic artery vasculitis   absent pulse, stroke  
🗑
Takayasu's arteritis   pulseless disease; young Asian woman  
🗑
Giant cell arteritis   temporal artery granulomatous vasculitis; ipsilateral blindness (ophthalmic artery)  
🗑
Classical polyarteritis nodosa   muscular artery vasculitis with vessel thrombosis infarction  
🗑
Path findings   vessel inflammation at different stages; aneurysms from vessel weakness  
🗑
S/S   infarctions in kidneys, skin, GI tract, heart; HBsAg in 30%  
🗑
Diagnosis   angiography identifies aneurysms and thrombosis  
🗑
Kawasaki's disease   coronary artery vasculitis/thrombosis/aneurysms in children  
🗑
Kawasaki's disease|S/S   chest pain; desquamating rash; swelling hands/feet; cervical lymphadenopathy  
🗑
Kawasaki's disease|Rx   IV γ-globulin  
🗑
Buerger's disease (thromboangiitis obliterans)   smoker's digital vasculitis; digital infarction  
🗑
Raynaud's syndrome   digital vasculitis in PSS and CREST syndrome  
🗑
S/S   digital pain; white-blue-red color changes  
🗑
Cryoglobulinemia   protein gels in cold temperature; Raynaud's syndrome; HCV association  
🗑
S/S   acral cyanosis relieved by coming indoors  
🗑
Wegener's granulomatosis   association with c-ANCA; sinusitis, lung infarction, crescentic GN  
🗑
Microscopic polyangiitis   palpable purpura; crescentic GN; association with p-ANCA  
🗑
Henoch-Schönlein purpura   IgA-anti-IgA ICs; palpable purpura buttocks/legs; arthritis; IgA GN  
🗑
Serum sickness vasculitis   e.g., horse antivenin in Rx of rattlesnake envenomation  
🗑
Rocky Mountain spotted fever   tick borne  
🗑
Meningococcemia   sepsis causes petechia/ecchymoses; potential for Waterhouse Friderichsen syndrome  
🗑
Essential HTN blacks   defect in renal excretion of sodium; ↑ plasma volume, ↓ PRA  
🗑
Renovascular HTN   atherosclerosis renal artery in men; fibromuscular hyperplasia renal artery women  
🗑
S/S   epigastric bruit; ↑ PRA affected kidney, ↓ PRA unaffected kidney  
🗑
Endocrine HTN   1º HPTH, Graves/hypothyroidism, Cushing's, 1º aldosteronism, phaeochromocytoma  
🗑
Hypertension   LVH MC complication; AMI MC COD followed by stroke and renal failure  
🗑
Afterload   resistance ventricles contract against  
🗑
Preload   volume ventricles must eject  
🗑
Concentric LVH   increased afterload; e.g., essential HTN, aortic stenosis  
🗑
LVH with dilation/hypertrophy   increased preload; e.g., valve regurgitation; left to right shunts  
🗑
LHF   forward failure; pulmonary edema, pillow orthopnea, paroxysmal nocturnal dyspnea  
🗑
Systolic dysfunction   LHF due to decreased ventricular contractility (ischemia)  
🗑
Diastolic dysfunction   LHF due to decreased ventricular compliance (hypertrophy)  
🗑
RHF   backward failure; ↑ venous hydrostatic pressure; neck vein distention, hepatomegaly, edema  
🗑
ACE inhibitors   decrease afterload and preload in heart failure  
🗑
Diuretics in CHF   reduce preload  
🗑
Non-pharmacologic Rx in CHF   restrict salt and water  
🗑
AMI   MC COD in United States; left anterior descending coronary artery thrombosis MCC  
🗑
Exertional angina   coronary artery atherosclerosis; subendocardial ischemia; ST depression  
🗑
Prinzmetal's angina   coronary artery vasospasm; transmural ischemia; ST elevation  
🗑
Sudden cardiac death   death within 1 hr of symptoms  
🗑
Path findings   severe coronary artery atherosclerosis; absence of occlusive thrombosis  
🗑
LAD coronary artery   anterior portion left ventricle, anterior 2/3rds IVS  
🗑
RCA   posterior portion left ventricle and papillary muscle, inferior 1/3rd IVS, right ventricle  
🗑
AMI   rupture of inflammatory plaque produces platelet thrombus  
🗑
Ventricular fibrillation   MC COD in AMI  
🗑
AMI   no gross changes until 24 hrs  
🗑
S/S AMI   retrosternal pain radiating down arms, diaphoresis  
🗑
AMI ruptures   3rd-7th day  
🗑
Anterior wall rupture   MC type; LAD thrombosis; cardiac tamponade  
🗑
Posteromedial papillary muscle rupture   RCA thrombosis; mitral regurgitation with LHF  
🗑
IVS rupture   LAD thrombosis; left to right shunt; RHF  
🗑
Mural thrombus   anterior AMI; danger embolization  
🗑
Pericarditis   first week in transmural AMI; 6 wks later autoimmune  
🗑
S/S   friction rub; leaning forward relieves pain  
🗑
Ventricular aneurysms   late manifestation of AMI; precordial systolic bulge; CHF MC COD  
🗑
Right ventricular infarction   RCA thrombosis; hypotension, RHF, preserved left ventricular function  
🗑
Diagnosis of AMI   CK-MB and troponins; CK-MB absent by 3 days; troponins last 7-10 days  
🗑
LDH isoenzymes   no longer used; LDH 1/2 flip indicates AMI  
🗑
Reinfarction   reappearance CK-MB after 3 days  
🗑
ECG findings in AMI   inverted T waves; ST elevation; Q waves  
🗑
Ejection fraction   EF = stroke volume/left ventricular end-diastolic volume; 80/120 = 0.66  
🗑
By-pass surgery   use internal mammary artery and saphenous veins ("arterialize" after 10 yrs)  
🗑
Angioplasty complication   localized dissection with thrombosis  
🗑
Umbilical vein   highest O2 saturation  
🗑
Ductus arteriosis in fetus   shunts blood from pulmonary artery to aorta; PGE keeps it open  
🗑
Ductus arteriosus in newborn   closes and becomes ligamentum arteriosum  
🗑
Eisenmenger's syndrome   cyanosis due to reversal of left to right shunt  
🗑
VSD   MC congenital heart disease; ↑ SaO2 right ventricle (RV), pulmonary artery (PA)  
🗑
ASD   patent foramen ovale; ↑ SaO2 right atrium (RA), RV, PA; MC adult congenital heart disease  
🗑
Down syndrome   endocardial cushion defect (combined ASD and VSD)  
🗑
PDA   machinery murmur; close with indomethacin; ↑ SaO2 PA  
🗑
Tetralogy of Fallot   degree of pulmonic stenosis determines if cyanosis is present  
🗑
Tetralogy of Fallot   ↓ left ventricle, aorta  
🗑
Tetralogy of Fallot   ASD and PDA are cardioprotective  
🗑
Complete transposition   cyanosis; aorta empties RV; PA empties left ventricle  
🗑
Complications cyanotic heart disease   2° polycythemia; infective endocarditis; metastatic abscesses  
🗑
Pre-ductal coarctation   Turner's syndrome  
🗑
Post-ductal coarctation   constriction distal to ligamentum arteriosum  
🗑
S/S   upper extremity HTN; claudication; rib-notching; activation RAA also causes HTN  
🗑
Acute rheumatic fever   type II hypersensitivity; group A streptococcus pharyngeal infection  
🗑
Acute rheumatic fever   sterile vegetations mitral valve (regurgitation); myocarditis with Aschoff nodule  
🗑
S/S   polyarthritis (MC), carditis, erythema marginatum, rheumatoid nodules, chorea  
🗑
Mitral stenosis   chronic rheumatic fever; opening snap followed by mid-diastolic rumble  
🗑
Mitral stenosis   left atrial dilation hypertrophy - atrial fibrillation, thrombus, pulmonary edema, RHF  
🗑
MVP   myxomatous degeneration of mitral valve; common in Marfan syndrome, Ehlers Danlos  
🗑
Mitral valve prolapse|S/S   mid-systolic click followed by a murmur; palpitations, chest pain, rupture of chordae  
🗑
MVP click/murmur close to S1   decrease preload (stand, Valsalva, anxiety)  
🗑
MVP click/murmur close to S2   increase preload (supine, squat, clench fist)  
🗑
Mitral regurgitation   pansystolic murmur; S3 and S4 common  
🗑
Causes   LHF, infective endocarditis, acute rheumatic fever  
🗑
Aortic stenosis   systolic ejection murmur; syncope and angina with exercise; hemolytic anemia  
🗑
Aortic stenosis murmur increased preload   worsens obstruction and increases murmur intensity  
🗑
Aortic stenosis murmur decreased preload   decreases obstruction and decreases murmur intensity  
🗑
Causes   bicuspid aortic valve; age-related sclerosis  
🗑
Aortic regurgitation   bounding pulses; early diastolic blowing murmur  
🗑
Austin Flint murmur   diastolic murmur; regurgitant flow on anterior leaflet mitral valve  
🗑
Significance Austin Flint murmur   sign for AV replacement  
🗑
Causes aortic regurgitation   essential HTN, infective endocarditis, acute rheumatic fever, dissection  
🗑
Tricuspid regurgitation   pansystolic murmur ↑ intensity with inspiration  
🗑
Causes   endocarditis IV drug abuse; RHF; carcinoid heart disease  
🗑
Carcinoid heart disease   tricuspid regurgitation, pulmonic stenosis  
🗑
Infective endocarditis (IE)   Streptococcus viridans MCC; Staphylococcus aureus MCC IVDA  
🗑
IE prosthetic heart valve   Staphylococcus epidermidis (coagulase negative)  
🗑
IE ulcerative bowel disease   Streptococcus bovis  
🗑
S/S   IC vasculitis-Roth spot, splinter hemorrhages; regurgitant murmurs; metastatic abscesses  
🗑
Lab findings   positive blood culture Libman Sacks endocarditis  
🗑
Coxsackievirus   MCC of myocarditis (lymphocyte infiltrate in myocardium) and pericarditis  
🗑
Parasitic cause myocarditis   leishmania in Chagas disease  
🗑
Pericardial effusion   all chamber pressures are uniformally increased  
🗑
S/S   muffled heart sounds, pulsus paradoxus, inspiratory neck vein distention  
🗑
Dx and Rx   echocardiogram, pericardiocentesis, respectively  
🗑
Pulsus paradoxus   drop in blood pressure >10 mmHg with inspiration  
🗑
Constrictive pericarditis   TB MCC worldwide; pericardial knock  
🗑
Congestive cardiomyopathy   generalized chamber enlargement; low ejection fraction  
🗑
Causes   postpartum, cardiotoxic drugs, hypothyroidism, alcohol  
🗑
Hypertrophic cardiomyopathy   MCC of sudden death in young person (due to conduction defects)  
🗑
Site of obstruction   anterior leaflet mitral valve drawn against asymmetric thickened IVS  
🗑
Effect decreased preload on systolic murmur   worsens obstruction and increases murmur intensity  
🗑
Effect increased preload on systolic murmur   reduces obstruction and decreases murmur intensity  
🗑
Restrictive cardiomyopathy   decreased compliance  
🗑
Causes   iron, amyloid, glycogen; sarcoidosis; tropical endocardial fibrosis  
🗑
Cardiac myxoma   benign tumor left atrium; embolization; syncope  
🗑
Cardiac rhabdomyoma   childhood tumor; association with tuberous sclerosis  
🗑
U wave   hypokalemia; MCC diuretic therapy (e.g., thiazides; loop diuretics)  
🗑
Peaked T wave   hyperkalemia; MCC renal failure  
🗑
ST depression   subendocardial ischemia (e.g., classical angina pectoris)  
🗑
ST elevation   transmural ischemia (e.g., AMI), pericarditis, ventricular aneurysm  
🗑
Atrial fibrillation   MC chronic arrhythmia; absent P waves; danger for embolization  
🗑
Ventricular premature beats   wide QRS complexes; MC arrhythmia in coronary care unit  
🗑
Ventricular fibrillation   MCC of death in an AMI  
🗑
Anterior AMI   Q waves in I and V1-V4  
🗑
Inferior AMI   Q waves in II, III, and aVF; right coronary artery thrombosis.  
🗑
Wolff-Parkinson-White   short PR interval with normal P wave; delta wave on upstroke of R wave  
🗑
Alveolar O2 calculation   % O2 breathing (713) - PCO2/0.8  
🗑
Increased A-a gradient   primary lung disease; left to right shunts in heart  
🗑
Forced vital capacity   total amount of air expelled after a maximal inspiration  
🗑
Forced expiratory volume/1 second (FEV1)   amount of air expelled in 1 second after maximal inspiration  
🗑
Choanal atresia   cyanotic when breast feeding; turns pink when crying  
🗑
Nasal polyps   allergic (MC; adults only), aspirin, cystic fibrosis  
🗑
Nasal polyp in a child   requires sweat test to exclude cystic fibrosis  
🗑
Triad asthma   patient on aspirin (pain syndrome) with nasal polyps, asthma  
🗑
Obstructive sleep apnea (OSA)   snoring with intervals of apnea (respiratory acidosis with hypoxemia)  
🗑
S/S   danger cor pulmonale; requires sleep test; Rx. O2 with continuous positive airway pressure  
🗑
Sinusitis   maxillary sinusitis MC in adults; ethmoiditis MC in children; S. pneumoniae MC  
🗑
Nasopharyngeal carcinoma   association with EBV; metastasize to cervical nodes  
🗑
Laryngeal carcinoma   smoking MCC; hoarseness; squamous cell carcinoma  
🗑
Resorption atelectasis   MCC of fever 24-36 hours after surgery  
🗑
S/S   ↓ percussion; absent fremitus, breath sounds; inspiratory lag; elevated diaphragm  
🗑
RDS   decreased production surfactant; airway collapse; hyaline membranes  
🗑
Type II pneumocytes   synthesize surfactant (lecithin, phosphatidylcholine); stored in lamellar bodies  
🗑
Surfactant   reduces surface tension in airways; ↑ synthesis cortisol, thyroxine; ↓ synthesis insulin  
🗑
Causes RDS   prematurity, maternal diabetes, C-section  
🗑
Maternal diabetes   maternal hyperglycemia → fetal hyperglycemia → fetal insulin which ↓ surfactant  
🗑
Complications RDS   O2 FR injury (blindness, bronchopulmonary dysplasia); necrotizing enterocolitis  
🗑
Typical community acquired pneumonia   Streptococcus pneumoniae MCC  
🗑
Typical pneumonia   bronchopneumonia, lobar pneumonia  
🗑
S/S   productive cough; consolidation - ↓ percussion, ↑ tactile fremitus  
🗑
Atypical community acquired pneumonia   interstitial pneumonia; Mycoplasma pneumoniae MCC  
🗑
S/S   low grade fever, non-productive cough, no signs consolidation  
🗑
Nosocomial pneumonia   Pseudomonas, aeruginosa MCC (respirators); others - S. aureus, E. coli  
🗑
Rhinovirus   MCC common cold; hand to mouth transmission  
🗑
Respiratory syncytial virus   MCC pneumonia and bronchiolitis in child  
🗑
Parainfluenza virus   MCC croup in child; trachea area of obstruction  
🗑
Cytomegalovirus   basophilic intranuclear inclusion surrounded by halo  
🗑
Influenza   superimposed pneumonia with S. aureus increases mortality  
🗑
Rubeola   Warthin-Finkeldey multinucleated giant cells  
🗑
Chlamydia pneumoniae   atypical pneumonia; association with coronary artery disease  
🗑
Chlamydia trachomatis   pneumonia in newborns; staccato cough; wheezing  
🗑
Coxiella burnetii   only rickettsia without a vector  
🗑
Mycoplasma pneumoniae pneumonia   crowded condition; cold agglutinins; azithromycin  
🗑
Streptococcus pneumoniae pneumonia   gram positive diplococcus; azithromycin  
🗑
Staphylococcus aureus pneumonia   tension pneumatocysts in children with cystic fibrosis  
🗑
Corynebacterium diphtheriae   toxin produces ADP ribosylation of elongation factor 2  
🗑
Haemophilus influenzae   exacerbation chronic bronchitis; acute epiglottis in children  
🗑
Inspiratory stridor child   croup, epiglottitis  
🗑
Pseudomonas aeruginosa   MCC of pneumonia and death in cystic fibrosis; green sputum  
🗑
Klebsiella pneumoniae   mucoid sputum in alcoholic  
🗑
Legionella pneumophila   silver stain; water coolers/mist (grocery produce, restaurants, zoo rain forest)  
🗑
Mycobacterium tuberculosis   strict aerobe; MC COD due to infectious disease worldwide  
🗑
Candida albicans   vessel invader; yeasts and pseudohyphae  
🗑
Cryptococcus immitis   pigeon excreta; narrow-based bud  
🗑
Aspergillus fumigatus   septate hyphae with fruiting body; fungus ball, extrinsic asthma, vessel invader  
🗑
Mucor species   non-septate; vessel invader; frontal lobe abscess in diabetic ketoacidosis  
🗑
Coccidioides immitis   Southwest deserts; inhale arthrospores in dust; spherule with endospores  
🗑
S/S   erythema nodosum (painful nodules lower legs)  
🗑
Histoplasma capsulatum   Ohio/central Mississippi river valley; excreta bats (spelunker), chickens  
🗑
H. capsulatum   simulates TB; yeasts phagocytosed by macrophages  
🗑
Blastomyces dermatitidis   overlaps histoplasmosis; broad-based buds; skin lesion simulates cancer  
🗑
Pneumocystis carinii   cysts and trophozoites; pneumonia in HIV; Rx. trimethoprim/sulfamethoxazole  
🗑
Primary TB   upper portion lower lobe, lower portion upper lobe  
🗑
Primary TB   Ghon focus (subpleural caseation); Ghon complex (spread to hilar nodes)  
🗑
Reactivation TB   cavitating lesion in upper lobe; kidney MC extrapulmonary site  
🗑
Mycobacterium avium intracellulare (MAI)   atypical TB; MC TB in AIDS  
🗑
CF   AR; 3 nucleotide deletion chromosome 7; defective CFTR (degraded in Golgi apparatus)  
🗑
S/S   pneumonia, malabsorption, males sterile; + sweat test; P. aeruginosa pneumonia MC COD  
🗑
Lung abscess   MCC aspiration oropharyngeal material (mixed aerobe/anaerobe); x-ray - air/fluid level  
🗑
Aspiration sitting   posterobasal segment right lower lobe  
🗑
Aspiration supine   superior segment right lower lobe  
🗑
Aspiration right side   right middle lobe, posterior segment right upper lobe  
🗑
Pulmonary thromboembolism   most derive from femoral vein  
🗑
Bronchial artery   branch of aorta/intercostal artery; protects against developing pulmonary infarction  
🗑
Saddle embolus   sudden death due to acute right heart strain  
🗑
S/S pulmonary infarction   dyspnea and tachypnea; pleuritic chest pain; pleural effusion  
🗑
Dx   ventilation/perfusion scan; respiratory alkalosis; hypoxemia  
🗑
Pain on inspiration   pleuritic inflammation; pulmonary embolus, pneumonia, pneumothorax  
🗑
Pathogenesis pulmonary hypertension (PH)   hypoxemia and respiratory acidosis  
🗑
Hypoxemia + respiratory acidosis   vasoconstriction pulmonary vessels; vasodilation cerebral vessels  
🗑
Causes PH   1° lung disease (COPD, restrictive), recurrent emboli, mitral stenosis, OSA, left-right shunts  
🗑
Cor pulmonale   PH + RVH  
🗑
S/S   dyspnea; accentuated P2 (PH); parasternal heave (RVH)  
🗑
Restrictive lung disease   ↓ compliance, ↑ elasticity; interstitial fibrosis/edema  
🗑
Restrictive lung disease (RLD)   ↓ all volumes and capacities; ↑ FEV1sec/FVC ratio  
🗑
ARDS   RLD; non-cardiogenic pulmonary edema due to alveolar injury  
🗑
ARDS   neutrophil destruction of type I and II pneumocytes; hyaline membranes  
🗑
Causes   septic shock (MC), aspiration gastric contents, severe trauma  
🗑
Pneumoconiosis   inhalation mineral dust causing interstitial fibrosis; particles <0.5 μm to reach alveoli  
🗑
Caplan syndrome   pneumoconiosis + rheumatoid nodules in lungs  
🗑
Coal worker's   "black lung" disease; progressive massive fibrosis; no increased incidence cancer or TB  
🗑
Silicosis   quartz; nodular opacities; foundry workers; ↑ incidence cancer and TB  
🗑
Sources asbestos   roofing material, old buildings (9/11), pipe-fitter shipyard  
🗑
Ferruginous bodies   asbestos fiber coated by iron  
🗑
Asbestosis   benign pleural plaques (MC); bronchogenic carcinoma (MC cancer); mesothelioma  
🗑
Mesothelioma   malignancy of serosa; no smoking association  
🗑
Sarcoidosis   RLD; MC non-infectious lung and liver granulomatous disease  
🗑
S/S   dyspnea, hilar adenopathy (non-caseating granulomas), uveitis, nodular skin lesions  
🗑
Lab findings   ↑ ACE, hypercalcemia (macrophages synthesize 1-α-hydroxylase)  
🗑
Kveim test   intradermal injection sarcoid antigens causes skin reaction  
🗑
Farmer's lung   RLD; lung reaction against thermophilic bacteria in moldy hay  
🗑
Silo filler's disease   RLD; reaction against nitrogen dioxide in fermenting corn  
🗑
Byssinosis   RLD; reaction against cotton, linen, hemp products in textile industry  
🗑
Goodpasture's syndrome   RLD; anti-BM antibodies; begins in lungs and ends in renal failure  
🗑
Collagen vascular RLD   SLE, rheumatoid arthritis, systemic sclerosis  
🗑
Drugs RLD   amiodarone, bleomycin, busulfan, cyclophosphamide, methotrexate, nitrofurantoin  
🗑
Obstructive lung disease   ↑ compliance, ↓ elasticity  
🗑
Obstructive lung disease   ↑ RV, TLC; ↓ TV, VC; ↓ FEV1sec and FVC; ↓ FEV1sec/FVC ratio  
🗑
Obstructive lung disease   asthma, emphysema, chronic bronchitis, bronchiectasis  
🗑
Asthma   extrinsic (type I hypersensitivity) and intrinsic types  
🗑
S/S   expiratory wheezing (inflamed terminal bronchioles); LTC4,-D4,-E4 bronchoconstrictors  
🗑
Charcot-Leyden crystals   derive from crystalline material in eosinophil granules  
🗑
Lab findings   initial respiratory alkalosis; respiratory acidosis requires intubation  
🗑
Emphysema   destruction elastic tissue respiratory unit; lung hyperinflation; smoking MCC; pink puffer  
🗑
Respiratory unit   respiratory bronchiole, alveolar duct, alveoli  
🗑
Radiograph emphysema   ↑ AP diameter; depressed diaphragms; vertical heart  
🗑
Pathogenesis   ↓ AAT, ↑ neutrophil destruction of elastic tissue  
🗑
Centriacinar emphysema   destruction/distention respiratory bronchioles upper lobe in smokers; THINK  
🗑
Panacinar emphysema   destruction/distention entire respiratory unit lower lobes; AAT deficiency  
🗑
Paraseptal emphysema   upper lobe destruction/distention alveolar ducts, alveoli; pneumothorax  
🗑
Lab findings   normal to decreased PCO2 (respiratory alkalosis)  
🗑
Chronic bronchitis   productive cough 3 months/2 consecutive years; blue bloater (cyanosis)  
🗑
Site of obstruction   terminal bronchioles (proximal to respiratory unit)  
🗑
Lab findings   respiratory acidosis/hypoxemia  
🗑
Bronchiectasis   obstruction/infection key causes; dilated bronchioles extend to periphery  
🗑
Causes   CF MCC, TB, immotile cilia syndrome  
🗑
Immotile cilia syndrome   absent dynein arm in cilia; sinusitis, infertility, bronchiectasis, situs inversus  
🗑
Central lung cancers   squamous cancer and small cell cancer; men > women  
🗑
Peripheral lung cancers   adenocarcinoma; women > men  
🗑
Squamous lung cancer   cavitate; secrete PTH-related protein  
🗑
Small cell carcinoma   neuroendocrine tumor; secrete ACTH and ADH  
🗑
Bronchioloalveolar carcinoma   no smoking relationship; lung consolidation resembling pneumonia  
🗑
Scar carcinoma   usually adenocarcinoma developing in old TB scar  
🗑
Bronchial carcinoid   low grade malignant; hemoptysis; rare cause carcinoid syndrome  
🗑
Metastatic lung cancer   more common than primary cancer; breast cancer MCC  
🗑
Pancoast tumor   squamous carcinoma posterior mediastinum; destruction superior cervical ganglion  
🗑
S/S   Horner's syndrome - lid lag, miosis, anhydrosis; lower brachial plexus injury  
🗑
Solitary coin lesion   granuloma MCC  
🗑
Superior vena caval syndrome   primary lung cancer obstructs vessel; venous congestion  
🗑
Anterior mediastinal masses   thymoma; nodular sclerosing Hodgkin's; teratomas  
🗑
Posterior mediastinal masses   usually neurogenic tumors of ganglia  
🗑
Myasthenia gravis   B cell hyperplasia of thymus MC abnormality; association with thymoma  
🗑
Thymoma   association with hypogammaglobulinemia, autoimmune disease, pure RBC aplasia  
🗑
Pleural effusions   transudates or exudates; CHF MCC  
🗑
Spontaneous pneumothorax   rupture subpleural or intrapleural bleb; air/pleural cavity pressure same  
🗑
S/S   pleuritic chest pain, dyspnea, tracheal shift ipsilateral side, absent breath sounds  
🗑
Tension pneumothorax   flap-like pleural tear; increased pleural cavity pressure; compression atelectasis  
🗑
S/S   as above except tracheal shift to opposite side  
🗑
Cleft lip/palate   failure of fusion of facial processes  
🗑
Herpes labialis   multinucleated giant cell with acidophilic intranuclear inclusions on Tzanck prep  
🗑
Hairy leukoplakia   EBV glossitis; pre-AIDS defining lesion; not precursor to cancer  
🗑
Mumps   bilateral parotitis; unilateral orchitis; ↑ amylase  
🗑
Diphtheria   pseudomembrane pharynx and trachea with cervical lymphadenopathy  
🗑
Congenital syphilis   notched central incisors  
🗑
Actinomycosis   anaerobic gram + filamentous bacteria; complication extracted dental abscess  
🗑
S/S   draining sinuses with sulfur granules  
🗑
Exudative tonsillitis   majority are viral; 20% group A streptococcus  
🗑
Oral thrush   common in newborn; pre-AIDS defining lesion; yeasts and pseudohyphae  
🗑
Dental caries   Streptococcus mutans  
🗑
Peutz-Jegher's syndrome   mucosal pigmentation; hamartomatous polyps  
🗑
Leukoplakia/erythroleukoplakia   biopsy to rule out squamous dysplasia or cancer  
🗑
Squamous cell carcinoma   smoking and alcohol association; lower lip MC site  
🗑
Smokeless tobacco   verrucoid squamous cell carcinoma  
🗑
Gum hyperplasia   phenytoin, pregnancy, scurvy  
🗑
Pleomorphic adenoma   MC benign tumor of salivary glands; parotid MC site  
🗑
Mucoepidermoid carcinoma   MC malignant tumor major and minor salivary glands  
🗑
Dysphagia for solids only   lesion obstructing esophagus; e.g., cancer, web  
🗑
Plummer-Vinson syndrome   iron deficiency anemia causes esophageal web, glossitis, achlorhydria (↓ HCl in gastric acid)  
🗑
Dysphagia for solids and liquids   motor abnormality; e.g., achalasia MCC, PSS or CREST syndrome  
🗑
TE fistula   polyhydramnios; proximal esophagus ends blindly; distal esophagus derives from trachea  
🗑
VATER syndrome   vertebral abnormalities, anal atresia, TE fistula, renal disease/radius abnormality  
🗑
Zenker's diverticulum   MC pulsion diverticulum of esophagus; halitosis (stinky breath, food gets stuck); near UES  
🗑
GERD   relaxation of lower esophageal sphincter (LES) with acid reflux  
🗑
GERD   MCC nocturnal cough and asthma  
🗑
AIDS esophagitis   Candida MC, CMV, HSV  
🗑
Barrett's esophagus   glandular metaplasia distal esophagus in GERD  
🗑
Complications of Barrett's   precursor for adenocarcinoma, stricture  
🗑
Esophageal varices   dilated left gastric vein; sign of portal hypertension due to cirrhosis  
🗑
Mallory Weiss syndrome   tear of distal esophagus from retching in alcoholic or bulimic  
🗑
Boerhaave's syndrome   rupture of distal esophagus from retching; pneumomediastinum  
🗑
Hamman's mediastinal crunch   pneumomediastinum (air in subcutaneous tissue)  
🗑
LES ganglion cells   contain VIP - relaxes LES  
🗑
Achalasia   failure of LES relaxation (no VIP); absent ganglion cells in the myenteric plexus  
🗑
S/S   aperistalsis/dilation of esophagus; regurgitation of undigested food at night  
🗑
X-ray achalasia   bird's beak appearance  
🗑
Acquired achalasia   Chagas' disease; leishmania destroy ganglion cells  
🗑
Distal adenocarcinoma esophagus   MC primary cancer; due to Barrett's esophagus  
🗑
Squamous cell carcinoma of esophagus   smoking MCC; alcohol also causes  
🗑
Melena   sign of upper GI bleed; acid changes Hb to hematin; peptic ulcer disease MCC  
🗑
Hematemesis   vomiting blood; peptic ulcers MCC  
🗑
Congenital pyloric stenosis   hypertrophy pyloric muscle; vomiting non-bile stained fluid in 2-4 weeks  
🗑
Acute hemorrhagic (erosive) gastritis   NSAIDs MCC  
🗑
Mucous barrier stomach   maintained by PGE; misoprostol PGE analog  
🗑
Type A chronic gastritis   due to PA; achlorhydria with ↑ serum gastrin  
🗑
Type B chronic gastritis   due to H. pylori; involves pylorus and antrum  
🗑
H. pylori   curved rod; urease producer; MCC PUD, adenocarcinoma, gastric lymphoma  
🗑
Gastric ulcer   lesser curvature pylorus and antrum; poor defense against acid; food aggravates pain  
🗑
Duodenal ulcer   never malignant; ↑ acid production; food relieves pain  
🗑
Perforated peptic ulcer   air under diaphragm causes pain in left shoulder  
🗑
Menetrier's disease   giant rugal hyperplasia; protein loss from increased mucus  
🗑
Zollinger-Ellison syndrome   malignant islet cell tumor secreting gastrin; part of MEN I syndrome  
🗑
S/S   PUD in usual locations; sometimes multiple ulcers  
🗑
Hypergastrinemia   ZE, achlorhydria, gastric distention, H2 or proton blockers; renal failure  
🗑
Leiomyoma   MC benign tumor of stomach  
🗑
Intestinal type adenocarcinoma   H pylori related; ↓ incidence; lesser curvature pylorus/antrum  
🗑
Diffuse type adenocarcinoma   linitis plastica; signet ring cells; Krukenberg tumors ovaries  
🗑
Gastric lymphoma   stomach MC site for extranodal lymphomas; H. pylori associated  
🗑
Malabsorption   steatorrhea; chronic pancreatitis, bile salt deficiency, small bowel disease  
🗑
Causes bile salt deficiency   liver disease, bile salt resins, cholestasis, bacterial overgrowth, Crohn's  
🗑
D-xylose screen   failure to reabsorb xylose indicates small bowel disease  
🗑
Calcification of pancreas   chronic pancreatitis cause of malabsorption  
🗑
Celiac disease   autoimmune disease; antibodies against gliadin in gluten; flat villi  
🗑
Celiac disease   association with dermatitis herpetiformis  
🗑
Whipple's disease   systemic infection; foamy macrophages with bacteria (PAS+ inclusions) in small bowel submucosa  
🗑
S/S   fever, polyarthritis, skin pigmentation  
🗑
Invasive diarrhea   Campylobacter jejuni MCC; positive fecal smear for leukocytes  
🗑
Secretory diarrhea   loss isotonic fluid; enterotoxins from E. coli and V. cholerae  
🗑
Osmotic diarrhea   hypotonic loss fluid; laxatives, lactase deficiency  
🗑
Rotavirus   MCC diarrhea in children  
🗑
Norwalk virus   MCC diarrhea in adults  
🗑
Cytomegalovirus   common cause diarrhea in AIDS; MCC cholecystitis and pancreatitis in AIDS  
🗑
Staphylococcus aureus   preformed toxin causes food poisoning; culture food  
🗑
Bacillus cereus   preformed toxin in fried rice and tacos; gram positive rods in stool  
🗑
Clostridium botulinum (adult)   preformed neurotoxin (blocks acetylcholine release); paralysis and mydriasis  
🗑
Clostridium botulinum (child)   colonization of bowel with release of neurotoxin; eating honey  
🗑
Clostridium difficile   pseudomembranous colitis; post-antibiotics; toxin assay stool; Rx metronidazole  
🗑
Shigella sonnei   produces dysentery (bloody diarrhea); associated with HUS  
🗑
Salmonella enteritidis   gastroenteritis; animal reservoirs - poultry, turtles  
🗑
Salmonella paratyphi   sepsis; osteomyelitis in HbSS  
🗑
Salmonella typhi   typhoid fever; human transmission; bradycardia, neutropenia, splenomegaly  
🗑
Carrier state site   gallbladder  
🗑
M. tuberculosis   MCC intestinal TB in United States (swallow TB); Peyer's patch site of infection  
🗑
Enterotoxigenic E. coli   secretory diarrhea (traveler's diarrhea); toxin stimulates guanylate cyclase  
🗑
Vibrio cholerae   secretory diarrhea; toxin stimulates adenylate cyclase to produce cAMP  
🗑
Oral Rx cholera   solution must contain glucose to reabsorb Na+ (co-transport)  
🗑
Yersinia enterocolitica   mesenteric lymphadenitis; sepsis in iron overload states  
🗑
Entamoeba histolytica   dysentery; trophozoites phagocytose RBCs; liver abscess; Rx metronidazole  
🗑
Cryptosporidium parvum   MCC diarrhea in AIDS; acid-fast oocysts  
🗑
Giardia lamblia   MC protozoal cause of diarrhea; cause of malabsorption; Rx metronidazole  
🗑
Trichuris trichiura   rectal prolapse in children  
🗑
Enterobius vermicularis   anal pruritus; urethritis in girls; no eosinophilia  
🗑
Ascaris lumbricoides   intestinal obstruction due to adult worms; no eosinophilia  
🗑
Necator americanus   hookworm; iron deficiency anemia  
🗑
Strongyloides stercoralis   rhabditiform larvae in stool not eggs  
🗑
Diphyllobothrium latum   fish tapeworm; vitamin B12 deficiency  
🗑
Signs of small bowel obstruction   colicky pain; constipation and obstipation  
🗑
Radiograph small bowel obstruction   air-fluid levels on x-ray  
🗑
MCC small bowel obstruction   adhesions from previous surgery  
🗑
Duodenal atresia   vomiting bile-stained fluid at birth; double bubble sign; Down syndrome  
🗑
Hirschsprung disease   absent ganglion cells in submucosal/myenteric plexus rectosigmoid  
🗑
S/S   proximal bowel dilated but peristalses; no stool in rectal vault  
🗑
Hirschsprung association   Down syndrome; Chagas disease  
🗑
Intussusception   terminal ileum telescopes into cecum; obstruction plus bloody diarrhea  
🗑
Meconium ileus   complication of cystic fibrosis  
🗑
Indirect inguinal hernia   second MCC of small bowel obstruction; common in weight lifting  
🗑
Gallstone ileus   obstruction of small bowel with gallstone + air in biliary tree  
🗑
Volvulus   MC due to sigmoid colon twisting around mesentery  
🗑
Direct inguinal hernia   protrudes through center of triangle of Hesselbach; no obstruction  
🗑
Umbilical hernia   common in black children; may entrap bowel in adults  
🗑
Sigmoid colon   MC site for polyps, cancer, diverticula  
🗑
Small bowel infarction   diffuse abdominal pain with bloody diarrhea  
🗑
Causes small bowel infarction   embolism (atrial fibrillation), thrombosis SMA or SMV  
🗑
Ischemic colitis   splenic flexure pain with bloody diarrhea  
🗑
Mesenteric angina   pain in splenic flexure 30 minutes after eating  
🗑
Angiodysplasia   submucosal dilation of venules in cecum; cause of hematochezia  
🗑
Hematochezia   massive loss of blood per rectum; diverticulosis MCC  
🗑
Meckel's diverticulum   persistence omphalomesenteric duct  
🗑
S/S   bleeding MC (iron deficiency in children), diverticulitis  
🗑
Meckel's diverticulitis   mimics acute appendicitis; cannot differentiate without radionuclide scan  
🗑
Sigmoid diverticulum   diverticulitis MC complication; MCC hematochezia and fistula formation  
🗑
Diverticulitis   "left-sided acute appendicitis"  
🗑
Ulcerative colitis   mucosal/submucosal ulceration; starts in rectum; crypt abscess; ↑ risk adenocarcinoma  
🗑
S/S   left lower quadrant crampy pain with bloody diarrhea  
🗑
UC associations   primary sclerosing cholangitis, seronegative HLA B27 + spondyloarthropathy  
🗑
Crohn's disease   transmural inflammation; terminal ileum involved 80%; granulomas; skip lesions  
🗑
S/S   colicky pain and diarrhea; fistulas (anal, bowl to bowel)  
🗑
Carcinoid tumor   appendix MC site; terminal ileum MC site for carcinoid syndrome  
🗑
Carcinoid syndrome   liver metastasis; flushing/diarrhea due to serotonin; increased urine 5-HIAA  
🗑
Tubular adenomas   precursor lesion colon cancer; size and number determine risk of malignancy  
🗑
Villous adenoma   greatest risk for colon cancer (30%); secrete mucus rich in protein and potassium  
🗑
Familial polyposis   AD with 100% penetrance for developing colon cancer  
🗑
Gardner's syndrome   AD, polyposis plus osteomas and desmoid tumors  
🗑
Turcot's syndrome   AD, polyposis plus brain tumors  
🗑
Colorectal cancer   second MC cancer and cancer killer in adults  
🗑
Left-sided colorectal cancer   obstruct; MC location rectosigmoid  
🗑
Right-sided colorectal cancer   bleed  
🗑
Acute appendicitis   due to lymphoid hyperplasia in children and obstruction by fecalith in adults  
🗑
External hemorrhoids   thrombose  
🗑
Internal hemorrhoids   bleed; prolapse out of rectum  
🗑
Urobilinogen (UBG)   breakdown product CB in bowel (color of stool)  
🗑
UBG   enterohepatic circulation to liver and kidney (color of urine)  
🗑
Alcoholic liver disease   serum AST>ALT; ↑ serum GGT  
🗑
Viral hepatitis   serum ALT>AST  
🗑
Cholestasis markers   serum AP and GGT  
🗑
Unconjugated bilirubin   macrophage degradation of heme; lipid soluble; never in urine  
🗑
Conjugated bilirubin (CB)   water soluble; never normal in urine  
🗑
% CB <20% (unconjugated)   Gilberts, spherocytosis, physiologic jaundice newborn, ABO/Rh HDN  
🗑
Gilbert's disease   AD; ↓ uptake and conjugation; bilirubin increases with fasting  
🗑
Physiologic jaundice newborn   unconjugated hyperbilirubinemia; begins on day three  
🗑
% CB 20-50%   viral/alcoholic hepatitis  
🗑
% CB >50%   bile duct obstruction (intra or extrahepatic); carcinoma head of pancreas  
🗑
Negative urine bilirubin + trace urobilinogen   normal urine  
🗑
Positive urine bilirubin, absent urobilinogen   obstructive jaundice  
🗑
Positive urine bilirubin + increased urobilinogen   hepatitis  
🗑
Negative urine bilirubin + increased urobilinogen   extravascular hemolytic anemia  
🗑
Markers of severity of liver disease   albumin, PT  
🗑
Hepatitis A   protective antibodies; day care centers, jails, homosexuals, traveling; not chronic  
🗑
Hepatitis B   protective antibodies; accidental needle stick, IVDA; hepatocellular carcinoma  
🗑
Hepatitis C   no protective antibodies; post-transfusion hepatitis; chronic state; hepatocellular carcinoma  
🗑
Hepatitis D   no protective antibodies; requires HBsAg to replicate  
🗑
Anti-HBs alone   vaccination  
🗑
Anti-HBs + anti-HBc-IgG   recovered from HBV  
🗑
HBsAg + HBeAg + HBVDNA + anti-HBc-IgM   acute HBV/chronic HBV infective carrier if >6 months  
🗑
Anti HBc-IgM alone   serologic gap; not infective  
🗑
HBsAg + anti-HBc-IgM   chronic HBV healthy carrier  
🗑
Fulminant hepatic failure   viral hepatitis and acetaminophen MCCs  
🗑
Spontaneous peritonitis   E. coli in adults; S. pneumoniae in children; complication of ascites  
🗑
Granulomatous hepatitis   TB MC bacteria  
🗑
Amebiasis   Entamoeba histolytica; flask shaped ulcers in cecum; liver abscess; Rx  
🗑
Echinococcosis   Echinococcus granulosis; sheep dog definitive host; man intermediate host  
🗑
Schistosomiasis   Schistosoma mansoni; adult worms in portal vein; "pipe stem cirrhosis"  
🗑
Clonorchiasis   Clonorchis sinensis; ingesting encysted larvae in fish; cholangiocarcinoma  
🗑
Congestive hepatomegaly (centrilobular necrosis)   "nutmeg" liver; RHF MCC  
🗑
Hepatic vein thrombosis   Budd-Chiari syndrome; painful hepatomegaly; ascites; portal hypertension  
🗑
Portal vein thrombosis   ascites, portal hypertension, no hepatomegaly  
🗑
Alcohol related disorders   fatty change; alcoholic hepatitis; cirrhosis  
🗑
Hypertriglyceridemia in alcoholics   ↑ synthesis of glycerol 3P (substrate for TG synthesis)  
🗑
Hypoglycemia in alcoholics   ↓ gluconeogenesis (↑ NADH causes pyruvate to convert to lactate)  
🗑
Ketoacidosis in alcoholics   ↑ lactate, ↑ ßOHB (acetyl CoA converted to AcAc and then ßOHB)  
🗑
Primary biliary cirrhosis   granulomatous destruction triad bile ducts; anti-mitochondrial antibody  
🗑
Primary sclerosing cholangitis   association with ulcerative colitis; MCC of cholangiocarcinoma  
🗑
Extrahepatic biliary atresia   neonatal cholestasis  
🗑
Drugs causing hepatitis   acetaminophen, isoniazid, halothane  
🗑
Anabolic steroids   intrahepatic cholestasis  
🗑
Estrogen/oral contraceptives   intrahepatic cholestasis; hepatic adenoma (intraperitoneal hemorrhage)  
🗑
Methotrexate   liver fibrosis, fatty change  
🗑
Liver angiosarcoma   vinyl chloride  
🗑
Hemochromatosis   AR; increased iron reabsorption; liver target organ  
🗑
S/S   cirrhosis; "bronze diabetes" - skin pigmentation + destruction of islet cells; malabsorption  
🗑
Lab   ↑ serum ferritin, iron, % saturation; ↓ TIBC  
🗑
Wilson's disease   AR disease; defect in copper excretion in bile and synthesis of ceruloplasmin  
🗑
S/S   cirrhosis, movement disorder (necrosis in putamen), Kayser Fleisher ring (Descemet's membrane)  
🗑
Lab   ↓ ceruloplasmin (causes ↓ total copper); ↑ serum/urine free copper  
🗑
HELLP syndrome   pre-eclampsia; Hemolytic anemia, ELevated transaminases, Low Platelets  
🗑
AAT deficiency in child   AR, cannot secrete AAT from liver cell; cirrhosis; hepatocellular carcinoma  
🗑
Reye syndrome   coma and microvesicular fatty change post viral infection; increased ammonia  
🗑
Cirrhosis   irreversible fibrosis; regenerative nodules; portal hypertension  
🗑
Causes cirrhosis   alcohol (MC), HBV/HCV, hemochromatosis, Wilson's, AAT deficiency, 1° biliary  
🗑
Hepatic encephalopathy   mental status changes; ↑ serum ammonia  
🗑
Portal hypertension   ascites; varices; splenomegaly; hemorrhoids; caput medusae  
🗑
Cause of ascites   portal hypertension; hypoalbuminemia; secondary aldosteronism  
🗑
Rx   use aldosterone blocker (acidosis increases loss ammonium in stool)  
🗑
Hyperestrinism in men   gynecomastia; spider angiomas; female hair distribution  
🗑
Lab findings cirrhosis   ↓ BUN, glucose, sodium, potassium, calcium (↓ vitamin D); ↑ PT  
🗑
Liver cell adenoma   estrogen related (steroids, oral contraceptives); intraperitoneal hemorrhage  
🗑
Liver cancer   metastasis MC cancer; lung cancer MC primary site  
🗑
Hepatocellular carcinoma   chronic HBV and HCV MCC; ↑ AFP; hepatic/portal vein invasion  
🗑
Cholangiocarcinoma   primary sclerosing cholangitis MCC, C.C sinensis  
🗑
Pathogenesis of cholesterol stones   bile with too much cholesterol and too little bile salts  
🗑
Black pigment stones   sign of extravascular hemolytic anemia (spherocytosis, HbSS)  
🗑
Acute cholecystitis   stone impacted in cystic duct; right upper quadrant colicky pain with radiation to shoulder  
🗑
Chronic cholecystitis   chemical inflammation  
🗑
Gallbladder cancer   risk factors - cholelithiasis and porcelain gallbladder  
🗑
Acute pancreatitis   causes - alcohol and gallstones; ↑ amylase and lipase (more specific)  
🗑
S/S   epigastric pain with radiation into back  
🗑
Sentinel loop   localized ileus of duodenum due to acute pancreatitis  
🗑
Pancreatic pseudocyst   abdominal mass; persistence of ↑ serum amylase >1 week  
🗑
Chronic pancreatitis   alcohol abuse, CF; malabsorption, pain, type I diabetes  
🗑
Pancreatic cancer   smoking MCC  
🗑
S/S   jaundice/acholic (gray/pale) stools; palpable gallbladder; superficial migratory thrombophlebitis (Trousseau's sign); ↑ CA 19-9  
🗑
First sign tubule cell dysfunction   inability to concentrate urine  
🗑
Fixed specific gravity   chronic renal failure; cannot concentrate or dilute urine  
🗑
Negative urine bilirubin + trace urobilinogen   normal urine  
🗑
Positive urine bilirubin, absent urobilinogen   obstructive jaundice  
🗑
Positive urine bilirubin + increased urobilinogen   hepatitis  
🗑
Negative urine bilirubin + increased urobilinogen   extravascular hemolytic anemia  
🗑
Positive urine nitrite + positive urine leukocyte esterase   urinary tract infection  
🗑
Sterile pyuria   positive urine leukocyte esterase but negative standard culture; TB, C. trachomatis  
🗑
Prerenal azotemia   ↑ BUN and creatinine; ↓ renal blood flow (e.g. heart failure, hypovolemia)  
🗑
Renal azotemia   ↑ BUN and creatinine due to intrinsic renal disease (acute tubular necrosis)  
🗑
Postrenal azotemia   ↑ BUN and creatinine due to obstruction to urine flow  
🗑
Serum BUN:creatinine ratio   <15:1 (renal failure); >15:1 (prerenal or postrenal azotemia)  
🗑
BUN 80 mg/dL:creatinine 8 mg/dL   ratio 10/1 - renal failure  
🗑
BUN 80 mg/dL:creatinine 2 mg/dL   ratio 40/1 - prerenal azotemia or postrenal azotemia  
🗑
Creatinine clearance   measures GFR  
🗑
Proteinuria   important sign of renal dysfunction  
🗑
RBC casts   nephritic type of glomerulonephritis  
🗑
WBC casts   acute pyelonephritis, acute tubulointerstitial nephritis  
🗑
Fatty casts with Maltese crosses   nephrotic syndrome  
🗑
Hyaline casts   normal unless associated with proteinuria  
🗑
Renal tubular cell casts   acute tubular necrosis  
🗑
Waxy or broad casts   chronic renal failure  
🗑
Cystinuria   hexagonal crystals  
🗑
Horseshoe kidney   Turner's syndrome; lower poles fused  
🗑
Renal dysplasia   MC childhood cystic disease; abnormal development; flank mass  
🗑
Maternal oligohydramnios   fetal juvenile polycystic kidney disease; Potter's facies in newborn  
🗑
Adult polycystic kidney disease   AD; hypertension MC sign; cerebral berry aneurysms  
🗑
Visceral epithelial cells   synthesize basement membrane  
🗑
Glomerular BM   negative charge due to heparan sulfate  
🗑
Nephritic syndrome   oliguria; RBC casts; hypertension; mild to moderate proteinuria  
🗑
Nephrotic syndrome   proteinuria >3.5 g/day; ascites and pitting edema; fatty casts; fusion of podocytes  
🗑
Immunofluorescence   linear (anti-glomerular BM antibodies); granular (IC deposition)  
🗑
IgA GN   MC GN; usually nephritic; episodic hematuria; mesangial IC (lgA-anti-IgA) deposits  
🗑
Post-streptococcal GN   nephritic; subepithelial deposits; skin/pharyngeal infections; anti-DNAase B  
🗑
SLE type IV GN   nephritic; subendothelial deposits; anti-DNA antibodies  
🗑
Crescentic GN   crescents from parietal cell proliferation; worst GN; Goodpasture's, Wegener's  
🗑
Goodpasture's   nephritic; anti-BM antibodies (glomerular + pulmonary capillary); crescentic GN  
🗑
S/S   young male with hemoptysis progressing to renal failure  
🗑
Minimal change disease (lipoid nephrosis)   MCC childhood nephrotic syndrome  
🗑
Lipoid nephrosis   podocyte fusion; loss of negative charge in glomerular BM  
🗑
Focal segmental glomerulosclerosis   nephrotic syndrome; AIDS and IV heroin abuse  
🗑
Membranous GN   MCC adult nephrotic syndrome; subepithelial deposits; epimembranous spikes  
🗑
Causes membranous GN   HBV, ACE inhibitors, cancer  
🗑
Type I MPGN   nephrotic; subepithelial deposits; HCV association; tram tracks  
🗑
Type II MPGN   nephrotic; C3 nephritic factor; intramembranous ICs (dense deposit disease)  
🗑
DM nodular glomerulosclerosis   microalbuminuria first sign  
🗑
DM glomerulosclerosis   nodules with collagen in mesangium; hyaline arteriolosclerosis of arterioles  
🗑
ACE inhibitors   inhibit angiotensin II vasoconstriction of efferent arterioles  
🗑
Alport's syndrome   XD hereditary nephritis with sensorineural hearing loss  
🗑
Ischemic ATN   prerenal azotemia MCC; renal tubular cell casts; BUN:creatinine ratio <15:1  
🗑
Ischemic ATN   disruption of BM in proximal tubule and thick ascending limb  
🗑
Nephrotoxic ATN   aminoglycosides, IVP dye, Pb/mercury poisoning  
🗑
Nephrotoxic ATN   proximal tubule dysfunction; intact BM  
🗑
Oliguria   prerenal azotemia, ATN, glomerulonephritis, postrenal azotemia  
🗑
Acute pyelonephritis   vesicoureteral reflux with ascending infection; WBC casts, fever, flank pain  
🗑
Chronic pyelonephritis   U-shaped scars overlying blunt calyces  
🗑
Drug-induced tubulointerstitial nephritis   type I/IV reaction; e.g., penicillin  
🗑
S/S   ARF, fever, rash, eosinophilia, eosinophiluria, WBC casts  
🗑
Analgesic nephropathy   aspirin plus acetaminophen; renal papillary necrosis; IVP with ring defect  
🗑
Myeloma kidney   BJ protein produces foreign body reaction in tubules  
🗑
Urate nephropathy   prevent by giving allopurinol prior to chemotherapy  
🗑
CRF   fixed specific gravity; BUN:creatinine <15:1; waxy and broad casts  
🗑
Renal osteodystrophy CRF   hypovitaminosis D (no 1-α-hydroxylase); produces osteomalacia  
🗑
Renal osteodystrophy CRF   osteoporosis from metabolic acidosis  
🗑
Renal osteodystrophy CRF   secondary HPTH with increased osteoclastic activity  
🗑
S/S CRF   pericarditis, prolonged bleeding time, normocytic anemia, pathologic fractures  
🗑
Benign nephrosclerosis   kidney of hypertension; shrunken kidneys due to hyaline arteriolosclerosis  
🗑
Malignant hypertension   renal failure; encephalopathy; BP >210/120 mm Hg; IV nitroprusside  
🗑
Renal findings   necrotizing arteriolitis; "flea bitten" kidney; hyperplastic arteriolosclerosis  
🗑
Renal infarction   pale infarcts; hematuria; common in polyarteritis nodosa  
🗑
Hydronephrosis   renal stone MCC; atrophy of cortex/medulla; postrenal azotemia  
🗑
Renal stones   most contain calcium (calcium oxalate/phosphate); hypercalciuria MC risk factor  
🗑
S/S   colicky pain radiating into groin, hematuria; x-ray usually shows stone  
🗑
Staghorn calculus   due to urease producing organisms (Proteus); alkaline urine pH; ammonia smell  
🗑
Angiomyolipoma   hamartoma; associated with tuberous sclerosis  
🗑
Renal cell carcinoma   smoking MCC; invasion renal vein/vena cava; lung, bone mets; yellow colored  
🗑
S/S   flank mass, hematuria; ectopic hormones (EPO, PTH related peptide), left-sided varicocele  
🗑
Renal pelvis transitional cell carcinoma   smoking MCC, phenacetin, aniline dyes, cyclophosphamide  
🗑
Wilm's tumor   hypertension, unilateral abdominal mass in child; aniridia/hemihypertrophy in AD types  
🗑
Urine draining from umbilicus   persistent urachus  
🗑
Retroperitoneal fibrosis   produces hydronephrosis  
🗑
Bladder extrophy   abdominal wall defect + epispadias  
🗑
Bladder diverticula   most commonly due to prostatic hyperplasia with urethral obstruction  
🗑
Acute cystitis   E. coli; females > males; no fever, flank pain, or WBC casts  
🗑
Bladder transitional cell carcinoma   smoking MCC, aniline dyes, cyclophosphamide; papillary  
🗑
S/S   hematuria; hydronephrosis  
🗑
Bladder adenocarcinoma   risk factors persistent urachus, extrophy  
🗑
Bladder squamous cell carcinoma   Schistosoma hematobium infection  
🗑
Hypospadias   ventral opening on penis due to failure closure of urethral folds  
🗑
Epispadias   dorsal opening on penis due to defect in genital tubercle  
🗑
Peyronie's disease   painful curvature penis due to fibromatosis  
🗑
Priapism   persistent/painful erection; HbSS  
🗑
Squamous cell carcinoma penis   HPV and lack of circumcision most important risk factors  
🗑
Cryptorchidism   undescended testis; risk for seminoma applies to cryptorchid testis and normal testis  
🗑
Orchitis   mumps usually unilateral (infertility uncommon)  
🗑
Epididymitis   <35 - N. gonorrhoeae, C. trachomatis; >35 - E. coli, P. aeruginosa  
🗑
S/S   scrotal pain relieved by elevation of scrotum (Prehn's sign)  
🗑
Varicocele   left-sided scrotal mass; spermatic vein drains into left renal vein; infertility common  
🗑
Varicocele   may be due to invasion of left renal vein by renal cell carcinoma  
🗑
Hydrocele   persistent tunica vaginalis; scrotum transilluminates  
🗑
Torsion of testicle   testicle high in canal; absent cremasteric reflex  
🗑
Testicular cancer   unilateral painless mass that does not transilluminate  
🗑
Risk factors   cryptorchid testis, Klinefelter's, testicular feminization  
🗑
Seminoma   MC cancer; radiosensitive; large cells with lymphoid infiltrate; small percentage have ↑hCG  
🗑
Spermatocytic variant   >65 yrs of age  
🗑
Embryonal carcinoma   hemorrhage/necrosis; hematogenous spread before lymphatic; ↑AFP, hCG  
🗑
Yolk sac tumor   MC testicular cancer in boys; ↑AFP  
🗑
Choriocarcinoma   most aggressive testicle cancer; ↑hCG  
🗑
Teratoma   more often benign in children than adult  
🗑
Teratocarcinoma   teratoma + embryonal carcinoma  
🗑
Malignant lymphoma   MC type in elderly; metastasis not primary cancer  
🗑
Prostate   DHT derived stimulation embryo; periurethral area - hyperplasia; peripheral area - cancer  
🗑
Prostatitis   perineal pain, fever; WBCs at end of voiding  
🗑
Benign prostatic hyperplasia   DHT/estrogen-mediated; glandular/smooth muscle hyperplasia  
🗑
S/S   all men develop; urethral obstruction MC (hesitancy, dribbling, nocturia), hematuria, dysuria Rx  
🗑
Prostate cancer   DHT-mediated; palpable with rectal exam; osteoblastic metastasis (↑ AP)  
🗑
PSA   sensitive but not specific for prostate cancer; ↑ in hyperplasia  
🗑
Kallmann's syndrome   absent GnRH, anosmia, absence of taste  
🗑
Impotence   failure to sustain an erection; psychogenic in most cases (erections present at night)  
🗑
Erection   parasympathetic response  
🗑
Ejaculation   sympathetic response  
🗑
Leydig cell failure   ↑ LH; ↓ testosterone, sperm count; normal FSH  
🗑
Seminiferous tubule failure   ↑ FSH (↓inhibin); ↓ sperm count; normal LH and testosterone  
🗑
Leydig and seminiferous tubule failure   ↑ FSH and LH; ↓ testosterone and sperm count  
🗑
Y chromosome   determines genetic sex  
🗑
Testosterone   develops seminal vesicles, epididymis, vas deferens  
🗑
Dihydrotestosterone (DHT)   develops prostate and male external genitalia  
🗑
Male pseudohermaphrodite   genetic male; phenotypically female  
🗑
Testicular feminization   XR; deficient androgen receptors; MCC male pseudohermaphrodite  
🗑
Klinefelter's syndrome   XXY; 1 Barr body; female secondary sex characteristics  
🗑
Herpes genitalis   recurrent painful vesicles; multinucleated squamous cells with intranuclear inclusions  
🗑
Human papilloma virus   condyloma acuminata; koilocytosis (wrinkled nuclei surrounded by a halo)  
🗑
Chlamydia trachomatis   metaplastic squamous cells with vacuoles containing elementary bodies  
🗑
S/S   non-specific urethritis, cervicitis, PID, ophthalmia neonatorum  
🗑
Neisseria gonorhoeae   urethritis, cervicitis, PID; ophthalmia neonatorum, gram negative diplococcus  
🗑
Ophthalmia neonatorum first week   N gonorrhoeae  
🗑
Ophthalmia neonatorum second week   C. trachomatis  
🗑
Lymphogranuloma venereum   C. trachomatis subtype  
🗑
S/S   scrotal/vulva lymphedema; granulomatous microabscesses; rectal strictures in females  
🗑
Chancroid   painful ulcer, adenopathy, Hemophilus ducreyi  
🗑
Granuloma inguinale   Calymmatobacterium granulomatis; raised ulceration but no lymphadenopathy  
🗑
Treponema pallidum   spirochete; produces vasculitis of arterioles (plasma cell infiltrate)  
🗑
Primary syphilis   painless chancre  
🗑
Secondary syphilis   rash on palms/soles; condyloma lata; generalized adenopathy  
🗑
Tertiary syphilis   neurosyphilis (e.g., tabes dorsalis), aortic arch aneurysm, gummas  
🗑
RPR/VDRL   reagin antibodies against cardiolipin; ↓ titer with Rx of syphilis  
🗑
RPR/VDRL   false positive with anticardiolipin antibodies (common in SLE)  
🗑
FTA-ABS   confirmatory test for syphilis; not distinguish active from treated disease  
🗑
FTA-ABS   remains positive after Rx  
🗑
Trichomonas vaginalis   flagellate protozoan; cervicitis/vaginitis; Rx metronidazole both partners  
🗑
Gardnerella vaginalis   vaginal pH >5; bacterial vaginosis; clue cells; Rx metronidazole  
🗑
Candida vaginitis   white, curd-like discharge; DM, antibiotics, pregnancy; Rx fluconazole  
🗑
Vulvar squamous cancer   MC vulvar cancer; HPV association  
🗑
Vulvar leukoplakia   biopsy to R/O squamous dysplasia/cancer  
🗑
Lichen sclerosis vulva   epidermal atrophy; slight risk for squamous cancer  
🗑
Squamous hyperplasia vulva   leukoplakia; no cancer risk  
🗑
Paget's disease   intraepithelial adenocarcinoma (mucin production) of vulva  
🗑
Malignant melanoma   vulva location; similar to Paget cells but not mucin positive  
🗑
Gartner's duct cyst   lateral wall vagina; persistent mesonephric duct  
🗑
Embryonal rhabdomyosarcoma   bloody, grape-like vaginal mass young girl  
🗑
Vaginal adenosis   maternal exposure to DES; precursor clear cell adenocarcinoma vagina  
🗑
Vaginal squamous cancer   usually extension of cervical cancer  
🗑
Rokitansky-Kiister-Hauser   absence of vagina and uterus  
🗑
Nabothian cysts   endocervical glands covered by metaplastic squamous epithelium  
🗑
Pathologic cervicitis   trichomonas, HSV-2, C. trachomatis (follicular cervicitis)  
🗑
Cervical Pap   superficial squamous (estrogen), intermediate (progesterone), parabasal (no hormone)  
🗑
Normal   70% superficial, 30% intermediate  
🗑
Atrophic   100% parabasal cells  
🗑
Hyperestrinism   100% superficial cells  
🗑
Pregnancy   100% intermediate cells  
🗑
Endocervical cells   sign of adequately performed Pap smear  
🗑
Cervical polyp   bleeding after intercourse; non-neoplastic  
🗑
Cervical dysplasia   begins in transformation zone; associated with low and high risk HPV  
🗑
Risk factors cervical dysplasia/cancer   early onset sexual activity; multiple partners; smoking; OC  
🗑
CIN   cervical intraepithelial dysplasia; mild, moderate, severe (in-situ)  
🗑
Cervical cancer   ↓ incidence (Pap smear); 45-yr-old; COD renal failure from obstruction of ureters  
🗑
S/S   cervical discharge; bleeding after intercourse  
🗑
Sequence to menarche   breast budding, growth spurt, pubic hair, axillary hair, menarche  
🗑
Proliferative phase cycle   estrogen-dependent; ↑estrogen inhibits FSH and stimulates LH  
🗑
Ovulation   day 14-I6; LH surge; subnuclear vacuoles; ↑body temperature  
🗑
Secretory phase cycle   progesterone-dependent  
🗑
Menses   drop in estrogen/progesterone stimulates apoptosis; plasmin prevents clotting  
🗑
FSH   stimulates follicle and aromatase synthesis in granulosa cells  
🗑
LH   stimulates androgen synthesis in proliferative phase and progesterone synthesis in secretory phase  
🗑
Day 21   day of implantation of fertilized egg  
🗑
Pregnancy   ↑plasma volume > RBC mass; ↑GFR; ↑thyroxine/cortisol (increased binding proteins)  
🗑
hCG   LH analogue produced by syncytiotrophoblast  
🗑
hCG   stimulates corpus luteum of pregnancy to synthesize progesterone for 8-10 weeks  
🗑
Estrone   estrogen of postmenopausal woman; aromatization of adrenal androstenedione  
🗑
Estradiol   estrogen of non-pregnant woman in reproductive life; aromatization of testosterone  
🗑
Estriol   estrogen of pregnancy  
🗑
Menopause   ↑ FSH (best screen; due to ↓estrogen), ↑LH  
🗑
S/S   secondary amenorrhea, hot flushes  
🗑
Hirsutism   ↑ hair in normal areas  
🗑
Virilization   hirsutism + male secondary sex characteristics (clitoromegaly)  
🗑
Test for hirsutism/virilization   ↑ testosterone - ovarian source; ↑DHEA-sulfate - adrenal source  
🗑
Polycystic ovarian syndrome (POS)   ↑ LH; ↓ FSH; ↑ estrogen and androgens  
🗑
S/S   hirsutism, oligomenorrhea, infertility; enlarged ovaries with subcortical cysts; LH:FSH >2:1  
🗑
Menorrhagia   excess menstrual flow; MCC iron deficiency in women  
🗑
Dysmenorrhea   painful menses; 1° PGF2α, 2° endometriosis  
🗑
DUB   bleeding related to hormone rather than anatomic causes  
🗑
Anovulatory DUB   menarche and perimenopause; estrogen excess without progesterone  
🗑
Ovulatory DUB   irregular shedding, inadequate luteal phase  
🗑
Primary amenorrhea   no menses by 16 years old  
🗑
Secondary amenorrhea   no menses for 3 months  
🗑
Amenorrhea-hypothalamic/pituitary dysfunction   ↓ FSH/LH; e.g., hypopituitarism  
🗑
Amenorrhea-ovarian dysfunction   ↑FSH/LH; e.g., Turner's syndrome  
🗑
Amenorrhea-end-organ disease   normal FSH/LH; e.g., imperforate hymen  
🗑
Asherman syndrome   surgical removal of stratum basalis  
🗑
Primary amenorrhea-normal secondary sex characteristics   constitutional delay MCC  
🗑
Primary amenorrhea-lack secondary sex characteristics   Turner's  
🗑
Turner's syndrome   XO; no Barr bodies; XO/XY types have gonadoblastomas; streak gonads (no eggs)  
🗑
S/S   newborn with lymphedema hands/feet; cystic hygroma in neck (web); short stature; 1° amenorrhea  
🗑
Secondary amenorrhea   pregnancy MCC; prolactinoma; anorexia nervosa; pituitary adenoma  
🗑
Asherman syndrome   removal of stratum basalis causing scarring; secondary amenorrhea  
🗑
Endometritis   group B streptococcus; intrauterine device (Actinomyces); chronic - plasma cells  
🗑
Endometrial polyp   menorrhagia; not a precursor for endometrial cancer  
🗑
Adenomyosis   functioning endometrial glands and stroma in myometrium; enlarged uterus  
🗑
Endometriosis   functioning glands and stroma outside uterus; reverse menses; ovary MC site  
🗑
S/S   dysmenorrhea, painful stooling, bowel obstruction; "powder burn" appearance  
🗑
Endometrial hyperplasia   unopposed estrogen; simple/complex types; precursor endometrial cancer  
🗑
Causes   obesity, estrogen Rx, polycystic ovarian syndrome  
🗑
Endometrial cancer   obesity, nulliparity, estrogen Rx, early menarche/late menopause; OC protective  
🗑
S/S   bleeding in postmenopausal woman  
🗑
Leiomyoma uterus   menorrhagia, obstructive delivery; not a precursor for leiomyosarcoma  
🗑
Leiomyosarcoma   MC sarcoma  
🗑
Ectopic pregnancy   PID MC risk factor; intraperitoneal hemorrhage; screen with ß-hCG  
🗑
Follicular cyst   MC ovarian mass in young woman  
🗑
Risk factors ovarian tumors   nulliparity and genetic factors; OC protective  
🗑
Serous ovarian tumors   surface-derived; ↑ bilaterality; psammoma bodies in malignant type  
🗑
Mucinous ovarian tumors   surface-derived; pseudomyxoma peritonei in malignant type  
🗑
Endometrioid carcinoma   resembles endometrial cancer; association with endometriosis  
🗑
Cystic teratoma   MC benign germ cell tumor (<1% malignant); hair/teeth; calcifications  
🗑
Dysgerminoma   MC malignant germ cell tumor; associated with streak gonads of Turners  
🗑
Yolk sac tumor   MC germ cell tumor young girl; ↑AFP; Schiller-Duval bodies  
🗑
Meigs syndrome   ovarian fibroma, ascites, right-sided pleural effusion  
🗑
Granulosa tumor   low grade malignant; hyperestrinism, Call Exner bodies  
🗑
Thecoma   benign; yellow color; hyperestrinism  
🗑
Leydig cell and Sertoli cell tumors   hyperandrogenism  
🗑
Gonadoblastoma   XY phenotype of Turner's  
🗑
Krukenberg tumors   metastatic stomach cancer; signet ring cells  
🗑
Single umbilical artery   ↑ incidence congenital defects  
🗑
Syncytiotrophoblast   lining of villi; produces hCG and human placental lactogen  
🗑
Human placental lactogen   responsible for mild glucose intolerance in pregnancy  
🗑
Abruptio placenta   retroplacental clot; painful bleeding; hypertension, cocaine, smoking  
🗑
Placenta previa   placenta implanted over cervical os; painless bleeding  
🗑
Placenta accreta   direct implantation into myometrium without intervening decidua; hysterectomy  
🗑
Twin placenta   monochorionic always identical twins; dichorionic may be identical or fraternal  
🗑
Siamese twins   monoamniotic monochorionic twin placenta  
🗑
Enlarged placenta   DM, Rh HDN, syphilis  
🗑
Complete mole   benign neoplasm of chorionic villi; dilated villi; no embryo; 46 XX (both male)  
🗑
S/S   preeclampsia in first trimester; ↑ incidence choriocarcinoma  
🗑
Partial mole   embryo present; 68 XXY; no transformation into choriocarcinoma  
🗑
Choriocarcinoma   malignancy of trophoblastic tissue (syncytiotrophoblast, cytotrophoblast)  
🗑
Risk factors   complete mole (MC), spontaneous abortion, normal pregnancy  
🗑
S/S   ↑hCG; lung metastasis; good prognosis  
🗑
Chorioamnionitis   group B streptococcus (S. agalactiae) infection  
🗑
Preeclampsia   abnormal placentation causing placental ischemia; ↑ in vasoconstrictors (ATII)  
🗑
S/S   hypertension, proteinuria, pitting edema; begins in third trimester  
🗑
Spontaneous abortion   50% have karyotype deformity (trisomy 16)  
🗑
Amniotic fluid   fetal urine  
🗑
Polyhydramnios   TE fistula, duodenal atresia, open neural tube defects  
🗑
Oligohydramnios   infantile polycystic disease  
🗑
↑ Serum AFP   open neural tube defect  
🗑
↓ Serum AFP   Down syndrome  
🗑
Urine estriol   fetal adrenal, placental, maternal liver involved in its production  
🗑
Down syndrome triad   ↑ ß-hCG, ↓ serum AFP, ↓ urine estriol  
🗑
Fibrocystic change   MC breast mass <50-yrs-old; atypical hyperplasia cancer risk; lumpy, painful breasts  
🗑
Sclerosing adenosis   component of FCC; involves terminal lobules often has microcalcifications  
🗑
Fibroadenoma   benign stromal tumor; MC movable mass in women <35-yrs-old  
🗑
Intraductal papilloma   benign tumor lactiferous duct/sinus; MCC bloody nipple discharge <50-yr-old  
🗑
Invasive ductal cancer   MCC breast mass in woman >50-yrs-old  
🗑
Breast cancer risk   unopposed estrogen; family history first-degree relatives  
🗑
Breast cancer   painless mass upper outer quadrant in woman >50-yrs-old  
🗑
Mammography   screening test to detect non-palpable masses  
🗑
Palpable breast mass   order fine needle aspiration (not a mammogram)  
🗑
Ductal carcinoma in situ   necrotic centers (comedo); microcalcifications common  
🗑
Paget's disease of breast   invasive ductal cancer into nipple; Paget's cells similar to vulvar Paget's  
🗑
Medullary carcinoma   bulky tumor with large cells and lymphoid infiltrate; more common in Pt with BRCA 1 mutation  
🗑
Inflammatory carcinoma   orange peel appearance; lymphatics blocked by tumor (lymphedema)  
🗑
Lobular cancer   MC cancer of terminal lobule; ↑ bilaterality  
🗑
Phyllodes tumor   low grade malignant tumor of stroma  
🗑
ER-PR positive tumors   tumors responding to hormones; candidate for tamoxifen (anti-estrogen)  
🗑
ERB-B2 oncogene positive breast cancer   aggressive breast cancer  
🗑
Gynecomastia   estrogen stimulation of male breast  
🗑
Gynecomastia   normal in newborn, puberty (no surgery), old age; (micronodular) cirrhosis MC pathologic cause  
🗑
Overactive endocrine syndrome   most often adenomas; use suppression tests (most do not suppress)  
🗑
Tumors that suppress   prolactinoma (bromocriptine), pituitary Cushings (high dose dexamethasone)  
🗑
Underactive endocrine syndrome   autoimmune destruction MCC; stimulation tests  
🗑
Hypopituitarism adults   non-functioning adenoma MCC, Sheehan's postpartum necrosis (stop lactation)  
🗑
Hypopituitarism in children   craniopharyngioma (Rathke's pouch remnant) MCC; visual field defects  
🗑
S/S ↓ FSH and LH   amenorrhea, ↓ testosterone in male  
🗑
Growth hormone functions   muscle growth, gluconeogenesis; release of insulin growth factor (IGF)  
🗑
IGF   synthesized in liver; bone and cartilage growth  
🗑
S/S ↓ GH/IGF in children   growth retardation; ↓ height and weight  
🗑
Sleep and arginine infusion   stimulation tests for GH and IGF  
🗑
S/S ↓ GH/IGF in adults   hypoglycemia  
🗑
S/S ↓ TSH   secondary hypothyroidism; ↓ T4, ↓ TSH; muscle weakness, dry skin  
🗑
S/S ↓ ACTH   secondary hypocortisolism; ↓ cortisol, ↓ ACTH; fatigue; hypoglycemia  
🗑
Metyrapone   stimulation test for ACTH reserve  
🗑
Metyrapone   blocks adrenal 11-hydroxylase → ↑ ACTH and 11-deoxycortisol (proximal to block)  
🗑
Metyrapone test ↓ ACTH and 11-deoxycortisol   pituitary/hypothalamic dysfunction  
🗑
Metyrapone test ↑ ACTH and 11-deoxycortisol   Addison's disease  
🗑
Diabetes insipidus   loss ADH (central), refractory to ADH (nephrogenic); always diluting urine  
🗑
Central diabetes insipidus (CDI)   ↓ UOsm and ↑ POsm with water deprivation; vasopressin causes ↑ UOsm > 50%  
🗑
Causes CDI   pituitary stalk transection, hypothalamic lesion (site for ADH synthesis)  
🗑
Nephrogenic diabetes insipidus (NDI)   ↓ UOsm and ↑ POsm with water deprivation; vasopressin causes ↑ UOsm < 50%  
🗑
Causes NDI   lithium, demeclocycline, nephrocalcinosis, severe hypokalemia  
🗑
Gigantism   GH secreting pituitary adenoma before epiphyses have fused  
🗑
Acromegaly   GH secreting pituitary adenoma after epiphyses have fused  
🗑
S/S acromegaly   cardiomyopathy; large hands, feet, jaw; hyperglycemia  
🗑
Prolactin   inhibited by dopamine  
🗑
Prolactinoma   MC pituitary tumor; secondary amenorrhea and galactorrhea; prolactin inhibits GnRH  
🗑
Rx   surgery or bromocriptine (dopamine analog)  
🗑
Other causes hyperprolactinemia   primary hypothyroidism, drugs  
🗑
Inappropriate ADH syndrome   hyponatremia <120 mEq/L; ↑ UOsm (always concentrating urine)  
🗑
Causes   small cell carcinoma lung, CNS injury, chlorpropamide  
🗑
Rx   restrict water; demeclocycline in small cell carcinoma  
🗑
Serum T4   ↑ or ↓ in free hormone or thyroid binding globulin (TBG)  
🗑
↑ Serum T4 and normal TSH   ↑ TBG; due to ↑ in estrogen  
🗑
↑ Serum T4 and ↓ TSH   thyrotoxicosis  
🗑
↓ Serum T4 and normal TSH   ↓ TBG; due to anabolic steroids  
🗑
↓ Serum T4 and ↑ TSH   primary hypothyroidism  
🗑
↓ Serum T4 and ↓ TSH   secondary hypothyroidism  
🗑
TSH   negative feedback with T4 and T3; best screening test  
🗑
I131 uptake   ↑ in Graves; ↓ in thyroiditis, patient taking excess thyroid, hypothyroidism  
🗑
Cold nodule   non-functioning nodule; no uptake I131  
🗑
Hot nodule   functioning nodule; ↑ uptake I131  
🗑
Thyroglossal duct cyst   midline cystic mass  
🗑
Branchial cleft cyst   cyst in anterolateral neck  
🗑
Acute/subacute thyroiditis   painful thyroid; early thyrotoxicosis; ↓ I131 uptake  
🗑
Hashimoto's thyroiditis   MCC hypothyroidism; HLA Dr3/Dr5; inhibitory IgG TSH receptor antibody  
🗑
Hashimoto's thyroiditis   ↑ anti microsomal and thyroglobulin antibodies  
🗑
S/S   muscle weakness, periorbital puffiness, ↓ reflexes, diastolic hypertension, constipation, dry skin  
🗑
Lab   ↓ T4, ↑ TSH  
🗑
Cretinism   maternal hypothyroidism before fetal thyroid developed, genetic disorder  
🗑
S/S   mental retardation; short stature and increased weight; coarse skin  
🗑
Thyrotoxicosis   any cause ↑ thyroid hormone activity; Graves disease, excess hormone, thyroiditis  
🗑
Hyperthyroidism   ↑ synthesis thyroid hormone; Graves disease and toxic nodular goiter  
🗑
Graves disease   autoantibody against TSH receptor (type II reaction); HLA Dr3  
🗑
S/S unique to Graves   exophthalmos, pretibial myxedema  
🗑
S/S thyrotoxicosis   tachycardia/atrial fibrillation, systolic hypertension, diarrhea, brisk reflexes  
🗑
Lab thyrotoxicosis   ↑ T4, ↓ TSH, ↑ glucose, ↑ calcium  
🗑
I131 uptake   ↑ Graves, toxic nodular goiter; ↓ thyroiditis, excess hormone, hypothyroidism  
🗑
Rx Graves disease   ß-blocker; drug to decrease hormone synthesis (propylthiouracil)  
🗑
Toxic nodular goiter   hyperthyroidism; develops out of a multinodular goiter; no exophthalmos  
🗑
Goiter   enlarged thyroid; iodine deficiency MCC; relative thyroid hormone deficiency  
🗑
S/S   rapid enlargement due to hemorrhage into cyst; Rx thyroxine  
🗑
Solitary thyroid nodule woman   most often benign (cyst)  
🗑
Solitary thyroid nodule man or child   often malignant  
🗑
Papillary carcinoma thyroid   MC thyroid cancer; radiation exposure; psammoma bodies  
🗑
Follicular carcinoma thyroid   invades blood vessels  
🗑
Medullary carcinoma thyroid   parafollicular cells; calcitonin; amyloid (calcitonin conversion)  
🗑
MEN I syndrome   3 P's; pituitary tumor, parathyroid adenoma, pancreatic tumor (ZE or ß-islet cell tumor)  
🗑
MEN IIa syndrome   2 P's; medullary carcinoma thyroid, pheochromocytoma, parathyroid adenoma  
🗑
MEN IIb syndrome   1 P; medullary carcinoma thyroid, pheochromocytoma, mucosal neuromas  
🗑
Alkalotic pH   tetany with normal total calcium, ↓ ionized calcium and ↑ PTH  
🗑
Hypoalbuminemia   ↓ total calcium, normal ionized calcium and PTH  
🗑
Tetany   ↓ ionized calcium level; threshold potential comes closer to resting potential  
🗑
S/S   thumb adducts into palm, twitching after tapping of facial nerve  
🗑
PTH   maintains ionized Ca2+; ↑ Ca2+ renal reabsorption; ↓ phosphate/bicarbonate reabsorption in kidneys  
🗑
Primary HPTH   ↑ Ca2+, hypophosphatemia, ↑ PTH  
🗑
Cause   adenoma MCC, hyperplasia, cancer  
🗑
S/S   renal stone, peptic ulcers, pancreatitis, hypertension, metastatic calcification  
🗑
Secondary HPTH   ↓ Ca2+, ↑ PTH; hypovitaminosis D from renal failure MCC  
🗑
Malignancy-induced hypercalcemia   ↑ Ca2+, ↓ PTH; all other non-parathyroid causes same results  
🗑
Causes hypercalcemia   osteolytic lesions, sarcoidosis, ↑ vitamin D, PTH-related peptide, myeloma  
🗑
Tertiary HPTH   hypercalcemia developing from secondary HPTH  
🗑
Primary hypoparathyroidism   ↓ Ca2+ and ↓ PTH  
🗑
Causes   previous thyroid surgery, autoimmune, DiGeorge syndrome  
🗑
S/S   tetany; calcification basal ganglia  
🗑
Pseudohypoparathyroidism   ↓ Ca2+ with normal to ↑ PTH; end-organ resistance to PTH  
🗑
Other causes ↓ Ca2+   hypomagnesemia (↓ PTH), ↓ vitamin D, DiGeorge  
🗑
↓ Ca2+ and ↓ PTH   primary hypoparathyroidism  
🗑
↓ Ca2+ and ↑ PTH   secondary hyperparathyroidism  
🗑
↑ Ca2+ and ↑ PTH   primary hyperparathyroidism  
🗑
↑ Ca2+ and ↓ PTH   malignancy induced hypercalcemia; other causes hypercalcemia  
🗑
Waterhouse-Friderichsen syndrome   meningococcemia with bilateral adrenal hemorrhage due to DIC  
🗑
Addison's disease   autoimmune destruction adrenal cortex MCC, adrenogenital syndrome, metastasis  
🗑
S/S   hypotension (salt loss), hyperpigmentation (ACTH), hypoglycemia  
🗑
Lab   ↓ sodium, ↓ cortisol, ↑ potassium, ↑ ACTH  
🗑
Adrenogenital syndrome   AR; enzyme deficiency; hypocortisolism; hyperpigmentation from ↑ ACTH  
🗑
21-Hydroxylase deficiency   ↑ 17 KS, ↓ 17 OH, lose salt, hypotension; female pseudohermaphrodite  
🗑
11-Hydroxylase deficiency   ↑ 17 KS, ↑ 17 OH, retain salt, hypertension; female pseudohermaphrodite  
🗑
17-Hydroxylase deficiency   ↓ 17 KS, ↓ 17 OH, retain salt, hypertension; male pseudohermaphrodite  
🗑
MCC Cushings   long-term corticosteroid therapy  
🗑
Tests Cushings syndrome   low/high dose dexamethasone suppression; urine free cortisol (best test)  
🗑
Normal dexamethasone suppression   cortisol analogue; ↓ ACTH and ↑ cortisol  
🗑
Pituitary Cushings   MCC Cushing's; ACTH secreting pituitary tumor  
🗑
Lab   low dose dexamethasone not suppress cortisol; high dose suppresses  
🗑
Adrenal Cushings   adrenal adenoma secreting cortisol; suppressed ACTH  
🗑
Lab   no suppression with low/high dose dexamethasone  
🗑
Ectopic Cushings   ACTH secreting small cell carcinoma of lung; high ACTH and cortisol levels  
🗑
Lab   no suppression with low/high dose dexamethasone  
🗑
S/S Cushings   purple stria, truncal obesity, hypertension, DM  
🗑
Primary aldosteronism   benign adenoma in zona glomerulosa  
🗑
S/S   hypertension and muscle weakness (hypokalemia), no pitting edema  
🗑
Lab   hypernatremia, hypokalemia, metabolic alkalosis, ↑ urine K+ and Na+  
🗑
Pheochromocytoma   benign tumor in adrenal medulla in adults  
🗑
Associations   von Hippel Lindau, neurofibromatosis, MEN IIa and IIb  
🗑
S/S   labile hypertension, anxiety, sweating, headache  
🗑
Lab   ↑ 24 hr urine for VMA and metanephrines  
🗑
Neuroblastoma   malignant tumor adrenal medulla child; widespread metastasis; hypertension  
🗑
ß-islet cell tumor (insulinoma)   benign tumor; hypoglycemia, ↑ insulin and C-peptide  
🗑
Patient taking excess insulin   hypoglycemia, ↑ insulin, ↓ C-peptide  
🗑
Glucagonoma   malignant α-islet cell tumor; hyperglycemia and rash  
🗑
Zollinger Ellison syndrome   malignant islet cell tumor secreting gastrin; peptic ulcers  
🗑
Somatostatinoma   malignant δ islet cell tumor; DM, malabsorption, cholelithiasis, achlorhydria  
🗑
VIPoma   malignant islet cell tumor; diarrhea, hypokalemia, achlorhydria  
🗑
DM   organ damage correlates with glycemic control  
🗑
Type 1   young, thin person; no insulin; HLA DR3/4; insulitis; islet cell antibodies; ketoacidosis  
🗑
Type 2   older person; obese; relative insulin deficiency (↓ insulin receptors, postreceptor problems)  
🗑
Type 2   family history; fibrotic islet cells with amyloid; hyperosmolar nonketotic coma  
🗑
↑ Non-enzymatic glycosylation   glucose attaches to amino acids in basement membranes  
🗑
Non-enzymatic glycosylation   ↑ vessel permeability producing hyaline arteriolosclerosis  
🗑
Osmotic damage   glucose converted into sorbitol by aldose reductase  
🗑
Osmotic damage   lens (cataracts), Schwann cell (neuropathy), pericytes retinal vessels (microaneurysms)  
🗑
Pathogenesis hyperglycemia   ↑ gluconeogenesis (most important), glycogenolysis  
🗑
Pathogenesis hyperlipidemia   no insulin to stimulate capillary lipoprotein lipase; ↑ chylomicrons/VLDL  
🗑
Pathogenesis ketoacidosis   ↑ oxidation fatty acids with excess acetyl CoA; liver synthesis ketone bodies  
🗑
Most commons due to DM   neuropathy, blindness, CRF, hyperglycemia, non-traumatic amputation  
🗑
Glycosylated HbA1c   measure of long term glycemic control (8-12 weeks)  
🗑
Gestational DM   ↑ placental size, human placental lactogen  
🗑
Complications   macrosomia (↑ muscle/fat from insulin), RDS, newborn hypoglycemia (↑ insulin)  
🗑
Hypoglycemia   insulin/oral hypoglycemics MCC, liver disease; carnitine deficiency  
🗑
Carnitine deficiency   no ß-oxidation of fatty acids; all cells compete for glucose  
🗑
Monosodium urate crystals (MSU)   yellow when parallel to slow ray of compensator  
🗑
Calcium pyrophosphate crystals (pseudogout)   blue when parallel to slow ray of compensator  
🗑
Osteoarthritis   degeneration articular cartilage; subchondral cysts; eburnation; osteophytes at margins  
🗑
Joints   weight bearing (femoral head); DIP joint (Heberden's nodes), PIP joints (Bouchard nodes)  
🗑
Neuropathic joint   2° to neurologic disease; DM, syringomyelia, tabes dorsalis  
🗑
Rheumatoid arthritis (RA)   female dominant; HLA Dr4  
🗑
RF   IgM antibody against Fc portion IgG; causes inflammation of synovial tissue  
🗑
Pannus   inflamed hyperplastic synovial tissue destroys articular cartilage; joint fusion  
🗑
Joints   MCP and PIP joints  
🗑
S/S   morning stiffness; ulnar deviation of hands; carpal tunnel (entrapped median nerve)  
🗑
Rx   methotrexate often used as initial therapy, aspirin  
🗑
Sjogren's syndrome   destruction lacrimal and minor salivary glands; RA; anti-SS-Ro/SS-La (SSa and SSb)  
🗑
S/S   dry eyes and dry mouth  
🗑
Caplan syndrome   pneumoconiosis + rheumatoid nodules in lungs  
🗑
Felty's syndrome   RA + splenomegaly with hypersplenism  
🗑
Gouty arthritis   underexcretion of uric acid; big toe first affected; tophus in soft tissue sign chronic gout  
🗑
Gout associations   alcohol, Pb poisoning  
🗑
Tophus   MSU crystals produce foreign body giant cell reaction next to joint  
🗑
Uricosuric agents   probenecid and sulfinpyrazone  
🗑
Allopurinol   ↓ synthesis uric acid; xanthine oxidase inhibitor  
🗑
Pseudogout   involves knee; linear calcification in articular cartilage  
🗑
Ankylosing spondylitis   HLA-B27 seronegative (RF negative) spondyloarthropathy; male dominant  
🗑
S/S   sacroiliitis; bamboo spine causing kyphosis; aortitis; uveitis  
🗑
Associations   C. trachomatis MC, psoriasis, ulcerative colitis, Shigella, Campylobacter, Yersinia  
🗑
Reiter's syndrome   HLA-B27; Chlamydia urethritis; arthritis; conjunctivitis; Achilles tendon periostitis  
🗑
Osteomyelitis children   hematogenous spread of Staphylococcus aureus to metaphysis  
🗑
Osteomyelitis in HbSS   Salmonella paratyphi  
🗑
Pseudomonas aeruginosa osteomyelitis   puncture of foot when wearing rubber foot wear  
🗑
Tuberculous osteomyelitis   usually involves vertebra (Pott's disease)  
🗑
Disseminated gonococcemia   female dominant; C6-C9 deficiency  
🗑
Disseminated gonococcemia   septic arthritis (knee); tendinitis/synovitis and skin pustules in feet/wrists  
🗑
Lyme disease   bite Ixodes tick; Borrelia burgdorjeri; reservoirs white footed mouse, white tailed deer  
🗑
Early S/S   erythematous concentric rash (erythema chronicum migrans), Rx doxycycline  
🗑
Late S/S   arthritis, Bell's palsy (often bilateral), myocarditis, Rx doxycycline  
🗑
Babesiosis   carried by Ixodes tick; Babesia are intraerythrocytic parasites; hemolytic anemia  
🗑
Cat bite   potential for Pasteurella multocida septic arthritis  
🗑
Osgood Schlatter's   inflammation proximal tibial apophysis at patellar tendon insertion; knobby knee  
🗑
Osteogenesis imperfecta   AD; ↓ synthesis type I collagen; pathologic fractures; blue sclera  
🗑
Blue sclera   reflection choroidal veins  
🗑
Achondroplasia   AD; impaired enchondral calcification and premature closure of epiphyses  
🗑
S/S   normal head/vertebral column, short extremities  
🗑
Osteopetrosis   AD/AR; osteoclast defect; too much bone; pathologic fractures  
🗑
Osteoporosis   ↓ bone mass and density; pathologic fractures  
🗑
Postmenopausal osteoporosis   estrogen deficiency - ↑ osteoclastic activity, ↓ osteoblastic activity  
🗑
S/S   vertebral compression fractures, Colles fracture  
🗑
Colles fracture   fractured distal radius with dinner fork appearance  
🗑
Prevention   estrogen (under investigation), calcium, vitamin D, stress exercises (walking, weight lifting)  
🗑
Aseptic necrosis femoral head   femoral head fracture, corticosteroids, sickle cell disease; MRI best test  
🗑
Scaphoid bone fracture   aseptic necrosis in wrist bone  
🗑
Volkmann's ischemic contracture   fracture of distal radius; damage to brachial artery and median nerve  
🗑
Legg-Perthe's disease   aseptic necrosis of ossification center (femoral head) in children  
🗑
Paget's disease   elderly males; lytic/blastic bone lesions produce thick, weak bone  
🗑
S/S   pathologic fractures; ↑ serum AP; ↑ risk for osteogenic sarcoma  
🗑
Osteoid osteoma   radiolucent lesion in cortex proximal femur; nocturnal pain relieved by aspirin  
🗑
Osteogenic sarcoma   adolescent male; RB suppressor gene association; distal femur; ↑ AP  
🗑
Radiograph   "sunburst" appearance, Codman's triangle  
🗑
Ewing's sarcoma   primitive neuroectodermal tumor; round cell tumor  
🗑
Radiograph   "onion skinning"  
🗑
Osteochondroma   MC benign bone tumor; exophytic growth off metaphysis of distal femur  
🗑
Chondrosarcoma   MC malignant cartilaginous tumor; pelvic bones, proximal femur  
🗑
Giant cell tumor   epiphysis distal femur/proximal tibia; giant cells + neoplastic mononuclear cells  
🗑
Muscle weakness   primary muscle disease, neurosynapse disease, neurogenic disease  
🗑
Duchenne's muscular dystrophy   XR; deficiency dystrophin; ↑ serum CK at birth; waddling gait  
🗑
Dystrophin   attaches portions of cell membrane to sarcomere; important in contraction  
🗑
Becker's dystrophy   XR, defective dystrophin  
🗑
Myotonic dystrophy   AD; trinucleotide repeat disorder; cannot release grip  
🗑
Myasthenia gravis   autoantibody against acetylcholine receptors (type II); thymic hyperplasia B cells  
🗑
S/S   diplopia at end of day first sign; dysphagia solids/liquids upper esophagus; thymoma  
🗑
Dupuytren's contracture   fibromatosis palmar fascia  
🗑
Lipoma   MC soft tissue tumor  
🗑
Liposarcoma   MC adult sarcoma  
🗑
Embryonal rhabdomyosarcoma   MC childhood sarcoma  
🗑
Autoimmune disease   loss of self-tolerance  
🗑
Serum ANA   greatest sensitivity for detecting SLE  
🗑
SLE   type III reaction; confirm with anti-dsDNA, anti-Sm  
🗑
S/S   malar rash, photophobia, joint pain, fibrinous pericarditis, nephritic GN  
🗑
Drug-induced lupus   procainamide, hydralazine; anti-histone antibodies  
🗑
Antiphospholipid antibodies   lupus anticoagulant, anti-cardiolipin antibodies; vessel thrombosis  
🗑
PSS   excess collagen; anti-topoisomerase antibodies  
🗑
S/S   dysphagia solids/liquids, Raynaud's, interstitial lung disease, renal failure  
🗑
CREST   centromere antibody/calcinosis; Raynaud; esophageal dysmotility; sclerodactyly; telangiectasia  
🗑
Dermatomyositis/polymyositis   ↑ serum CK; risk of malignancy  
🗑
Mixed connective tissue disease   anti-ribonucleoprotein antibody  
🗑
Antibody against acetylcholine receptor   myasthenia gravis  
🗑
Antibody against basement membrane   Goodpasture's syndrome  
🗑
Antibody against endomysium and gliadin   celiac disease  
🗑
Antibody against insulin and islet cell   type I diabetes  
🗑
Antibody against intrinsic factor and parietal cell   pernicious anemia  
🗑
Antibody against microsome and thyroglobulin   Hashimoto's thyroiditis  
🗑
Antibody against mitochondria   primary biliary cirrhosis  
🗑
Antibody against proteinase 3 of neutrophil (cANCA)   Wegener's granulomatosis  
🗑
Antibody against myeloperoxidase of neutrophils (pANCA)   microscopic polyangiitis  
🗑
Antibody against TSH receptor   Graves disease  
🗑
Ichthyosis vulgaris   ↑ thickness of stratum corneum; absent granular layer  
🗑
Solar lentigo   "liver spot" in elderly; increased melanocytes  
🗑
Senile purpura   trauma to fragile vessels on dorsum of hands; normal finding in elderly  
🗑
Acute eczema   weeping rash with vesicles  
🗑
Chronic eczema   dry, thickened, pruritic skin  
🗑
Atopic dermatitis   dry skin, eczema (type I reaction); children - face, intertriginous areas  
🗑
Allergic contact dermatitis   type IV hypersensitivity; poison ivy, nickel rash  
🗑
Contact photodermatitis   tetracycline; rash in sun exposed areas  
🗑
Superficial dermatophytoses   KOH preparation shows fungi located in stratum corneum  
🗑
Tinea capitis   Trichophyton tonsurans MCC (negative Wood's lamp)  
🗑
Tinea capitis child with dog   Microsporum canis (positive Wood's lamp)  
🗑
Tinea versicolor   hypopigmentation; Malassezia furfur; "spaghetti" (hyphae)/"meatball" KOH  
🗑
Seborrheic dermatitis   dandruff; Malassezia furfur  
🗑
Molluscum contagiosum   poxvirus; bowl-shaped with central depression filled with keratin  
🗑
Rubeola   Koplik's spots; Warthin-Finkeldey giant cells  
🗑
Rubella   teratogenic; rash; postauricular adenopathy; arthritis in adults  
🗑
Parvovirus   "slapped face"; RBC aplasia, aplastic anemia (HbSS), spontaneous abortions, arthritis  
🗑
Roseola   HSV-6; high fever and then rash  
🗑
Toxic shock syndrome   toxin-producing S. aureus; tampon wearing; hypotension, desquamating rash  
🗑
Scarlet fever   group A streptococcus with erythrogenic toxin; strawberry tongue  
🗑
Actinic (solar) keratosis   precursor for squamous cell carcinoma; recur when scrapped off  
🗑
Psoriasis   elevated salmon-colored plaques covered by silver-colored scales; nail pitting  
🗑
Pityriasis rosea   herald patch followed by rash in lines of cleavage  
🗑
Varicella   chickenpox; rash at different stages; Reye syndrome association  
🗑
Herpes zoster   vesicular rash following a sensory dermatome  
🗑
HSV and Varicella-zoster virus   remain latent in sensory ganglia  
🗑
Impetigo   group A streptococcus; honey crusted lesions on face  
🗑
Pemphigus vulgaris   autoimmune disease; IgG antibodies against intercellular attachment sites  
🗑
Pemphigus vulgaris   intraepidermal bullae; acantholytic cells; row of tombstones  
🗑
Bullous pemphigoid   autoimmune disease; IgG antibodies against basement membrane  
🗑
Bullous pemphigoid   subepidermal bullae  
🗑
Pemphigus vulgaris/bullous pemphigoid   type II hypersensitivity  
🗑
Dermatitis herpetiformis   autoimmune disease; IgA ICs; subepidermal bullae with neutrophils  
🗑
Dermatitis herpetiformis   association with celiac disease  
🗑
Erythema multiforme   vesicles and bullae; bullseye appearance  
🗑
Risk factors   drugs, M. pneumoniae infection  
🗑
Stevens Johnson syndrome   erythema multiforme involving mouth  
🗑
Acne vulgaris   androgen dependent (receptor on sebaceous glands)  
🗑
Acne vulgaris   Propionibacterium acnes lipases produce fatty acids causing inflammation  
🗑
Acne rosacea   pustular, erythematous lesion on face resembling malar rash  
🗑
Urticaria   type I and III reactions; type I due to mast cell release of histamine (drugs, fire ant bites)  
🗑
Angioedema   subcutaneous swelling  
🗑
Causes   ACE inhibitor (bradykinin); C1 esterase inhibitor deficiency (C2 and C4 decreased)  
🗑
Sporotrichosis   traumatic implantation of Sporothrix fungus into subcutaneous tissue  
🗑
Causes   rose gardener, lobster fisherman (sphagnum moss)  
🗑
S/S   chain of subcutaneous nodules  
🗑
Tuberculoid leprosy   intact cellular immunity (positive lepromin skin test); granulomas; no organisms  
🗑
S/S   autoamputation of digits; skin depigmentation and anesthesia  
🗑
Lepromatous leprosy   defective cellular immunity (negative lepromin skin test); no granulomas  
🗑
S/S   leonine face, erythema nodosum during treatment  
🗑
Histology   Grenz zone (zone free organisms) foamy macrophages with organisms  
🗑
Rx   dapsone  
🗑
Erythema nodosum   painful nodule on shins; subcutaneous fat inflammation  
🗑
Associations   coccidioidomycosis, TB, leprosy  
🗑
Keratoacanthoma   benign neoplasm; mimics squamous cancer; spontaneously resolves  
🗑
UVB light cancers   basal cell carcinoma, squamous cell carcinoma, malignant melanoma  
🗑
Vitiligo   autoimmune destruction melanocytes producing skin depigmentation  
🗑
Seborrheic keratosis   pigmented, wart-like lesion; "stuck on" appearance  
🗑
Leser-Trelat sign   multiple outcroppings seborrheic keratosis; consider stomach cancer  
🗑
Acanthosis nigricans   verrucoid pigmented lesion usually in axilla; associated with gastric cancer  
🗑
Chloasma   pregnancy mask due to increased melanocytes  
🗑
Nevocellular nevus   benign pigmented tumor modified melanocytes  
🗑
Histology   nevus cells proliferate along basal cell area, dermis, or both  
🗑
Dysplastic nevus   precursor for malignant melanoma  
🗑
Malignant melanoma   malignant tumor of melanocytes; most rapidly increasing cancer worldwide  
🗑
ABCD for melanoma   A, asymmetry; B, irregular border; C, color change; D, increased diameter  
🗑
Risk factors   severe sunburn at early age (MC), dysplastic nevi  
🗑
Radial growth phase   spreads laterally in epidermis/superficial dermis but does not result in metastasis  
🗑
Vertical growth   malignant cells penetrate into dermis; potential for metastasis  
🗑
Lentigo malignant melanoma   face of elderly  
🗑
Superficial spreading melanoma   lower extremities, back  
🗑
Nodular melanoma   aggressive tumor with no radial growth phase  
🗑
Acral lentiginous melanoma   palms, soles, under nails; may occur in blacks  
🗑
Prognosis   depends most on depth of invasion  
🗑
Prevention   sunscreen >15  
🗑
Porphyria cutanea tarda   photosensitive bullous disease; deficiency uroporphyrinogen decarboxylase  
🗑
S/S   hypertrichosis, fragile skin, port wine colored urine (uroporphyrins)  
🗑
Black widow (Latrodectus) envenomation   neurotoxin; abdominal muscle cramps  
🗑
Brown recluse (Loxosceles) envenomation   necrotoxin; skin ulcer  
🗑
CSF   choroid plexus in ventricles; enters subarachnoid space; removed by arachnoid granulations  
🗑
CSF   less protein and glucose than serum; scant number of cells; ↑ chloride  
🗑
Xanthochromia   yellow colored CSF due to bilirubin pigment; indicates subarachnoid hemorrhage  
🗑
Papilledema of optic nerve   sign of cerebral edema (intracranial hypertension)  
🗑
Uncal herniation   intracranial hypertension; medial portion temporal lobe through tentorium cerebelli  
🗑
S/S   midbrain hemorrhage; CN III palsy (pupil down/out); mydriasis  
🗑
Mydriasis in uncal herniation   compression of parasympathetic system  
🗑
Cerebellar tonsils herniate into foramen magnum   intracranial hypertension  
🗑
Hydrocephalus   ↑ CSF volume with distention of ventricles  
🗑
Non-communicating   blockage aqueduct Sylvius MCC newborn  
🗑
Communicating   choroid plexus papilloma; scarring of arachnoid granulations  
🗑
Adults with hydrocephalus   progressive dementia, wide-based gait, urinary incontinence; THINK  
🗑
Open neural tube defects   folate must be adequate before pregnancy; ↑ AFP  
🗑
Spina bifida occulta   dimple overlying skin L5-S1; vertebral arch not completely closed  
🗑
Meningocele   vertebral defect with meninges  
🗑
Meningomyelocele   vertebral defect with meninges and spinal cord  
🗑
Arnold Chiari syndrome   elongation medulla/cerebellar tonsils through foramen magnum  
🗑
S/S   hydrocephalus, syringomyelia, meningomyelocele  
🗑
Dandy Walker syndrome   hypoplasia of cerebellar vermis; hydrocephalus  
🗑
Syringomyelia   enlarged cervical cord; fluid filled cyst in cervical spinal cord  
🗑
S/S   loss pain/temperature upper extremities (spinothalamic); motor loss in hands (anterior horn cells)  
🗑
Tuberous sclerosis   AD; mental retardation; hamartomas CNS/kidney; shagreen patches skin  
🗑
Tuberous sclerosis   angiomyolipomas kidneys; rhabdomyoma of heart  
🗑
Neurofibromatosis   AD; pigmented neurofibromas; cafe au lait spots  
🗑
Associations   pheochromocytoma, brain tumors, acoustic neuromas  
🗑
Meningitis   nuchal rigidity  
🗑
CSF findings viral meningitis   ↑ CSF protein, normal CSF glucose, ↑ lymphocytes  
🗑
CSF findings bacterial meningitis   ↑ CSF protein, ↓ CSF glucose, ↑ neutrophils  
🗑
Encephalitis   inflammation of brain; mental status abnormalities; coma  
🗑
Coxsackievirus   MCC viral meningitis  
🗑
HSV-1   hemorrhagic necrosis in temporal lobes  
🗑
Rabies   skunk and bat common vectors; Negri bodies in neurons; hydrophobia; flaccid paralysis  
🗑
CMV   intranuclear inclusions; periventricular calcification in congenital infection  
🗑
Polio virus   destruction of anterior horn cells; flaccid paralysis  
🗑
Subacute sclerosing panencephalitis   slow virus disease due to rubeola (measles virus)  
🗑
Progressive multifocal leukoencephalopathy   slow virus disease due to JC virus; common in AIDS  
🗑
Creutzfeldt-Jakob disease   prions; spongiform encephalopathy  
🗑
Risk factors   contact with human brain or contaminated beef (bovine disease)  
🗑
Meningitis newborn   Streptococcus agalactiae (group B) MCC; E. coli, 2nd MCC  
🗑
Listeria monocytogenes   newborn meningitis; gram + rods; pregnant mother should avoid soft cheeses  
🗑
Neisseria meningitidis   MCC meningitis 1 month - 18-yrs-old; petechia and DIC characteristic  
🗑
Streptococcus pneumoniae   MCC meningitis >18-yrs-old  
🗑
Mycobacterium tuberculosis   complication primary TB; base of brain meningitis with vasculitis  
🗑
Neurosyphilis   CSF with positive VDRL  
🗑
Meningovascular syphilis   vasculitis causing strokes  
🗑
General paresis   syphilis with dementia and brain atrophy  
🗑
Tabes dorsalis   posterior root ganglia/posterior column; ataxia; absent deep tendon reflexes; Argyll-Robertson pupil  
🗑
Argyll-Robertson pupil   pupil accommodates but does not react to direct light; THINK  
🗑
Cryptococcus neoformans   MC opportunistic CNS fungal disease; positive India ink  
🗑
Mucor species   frontal lobe abscess in diabetic ketoacidosis  
🗑
Toxoplasma gondii   MCC space occupying lesion in AIDS; avoid cat litter and raw meat in pregnancy  
🗑
Congenital toxoplasmosis   calcification basal ganglia; blindness; mental retardation  
🗑
Naegleria and Acanthamoeba   amoeba in fresh water; meningoencephalitis  
🗑
Taenia solium   pork tapeworm; adult with worms definitive host; adult with larva intermediate host  
🗑
Cysticercosis   larval form of T. solium; produces blindness and calcified cysts in CNS (seizures)  
🗑
Coup injuries   contusions at site of injury  
🗑
Contrecoup injuries   contusion on opposite side of injury; frontal and temporal lobes  
🗑
Epidural hematoma   temporoparietal skull fracture; tear middle meningeal artery  
🗑
Subdural hematoma   tear bridging veins; venous blood clot; fluctuating levels of consciousness  
🗑
Hypoxic injury   neurons more susceptible to damage than neuroglial cells  
🗑
Laminar necrosis   liquefactive necrosis at watershed areas in cortex  
🗑
Atherosclerotic stroke   pale infarction (liquefactive necrosis) extending to periphery of cerebral cortex  
🗑
Causes atherosclerotic stroke   thrombosis of middle cerebral artery or carotid artery  
🗑
MCA stroke   contralateral weakness/sensory loss; expressive aphasia if left hemisphere stroke  
🗑
Amaurosis fugax   loss vision described as curtain going down and then up  
🗑
Cause   embolus atherosclerotic plaque to branch of retinal artery (Hollenhorst plaque)  
🗑
Vertebrobasilar stroke   vertigo, ataxia, ipsilateral sensory loss face/contralateral hemiparesis/sensory  
🗑
Embolic stroke   hemorrhagic infarction extending to periphery cerebral cortex due to embolization  
🗑
Intracerebral hemorrhage   complication hypertension  
🗑
Cause of intracerebral hemorrhage   rupture of aneurysm of lenticulostriate vessels  
🗑
Location of intracerebral hemorrhage   basal ganglia MC site  
🗑
Subarachnoid hemorrhage   rupture of congenital berry aneurysm; severe occipital headache  
🗑
Lacunar stroke   microinfarctions; due to hyaline arteriolosclerosis (hypertension, diabetes)  
🗑
Pure motor stroke   posterior limb internal capsule  
🗑
Pure sensory stroke   thalamus  
🗑
Multiple sclerosis   autoimmune destruction myelin sheath/oligodendrocytes; plaques in white matter  
🗑
S/S   scanning speech, intention tremor, nystagmus, paresthesias, weakness  
🗑
Bilateral internuclear ophthalmoplegia   multiple sclerosis; demyelination MLF  
🗑
CSF with oligoclonal bands   sign of demyelination  
🗑
Central pontine myelinolysis   rapid intravenous correction of hyponatremia in alcoholic  
🗑
Alzheimer's disease   MCC dementia Alzheimer's disease  
🗑
Alzheimer's disease   ↑ amyloid-ß destroys neurons; occipital lobe spared  
🗑
Alzheimer's disease   ↑ density of neurofibrillary tangles and senile plaques  
🗑
Down syndrome   develop Alzheimer's disease at early age; 3 functioning chromosome 21s  
🗑
Apo E gene allele ε4   gene product has high affinity for amyloid-ß  
🗑
Parkinson's disease   depigmentation substantia nigra neurons; Lewy bodies; ↓ dopamine  
🗑
S/S   extrapyramidal (muscle rigidity), resting tremor, festinating (shuffling) gait  
🗑
Causes   CO poisoning, Wilson's, MPTP (meperidine derivative), drugs  
🗑
Huntington's disease   AD; atrophy of the head of the caudate nucleus; trinucleotide repeat disorder (anticipation)  
🗑
S/S   movement disorder; dementia  
🗑
Amyotrophic lateral sclerosis (ALS)   degeneration of lower/upper motor neurons; no sensory changes  
🗑
Werdnig Hoffman disease   childhood type of ALS  
🗑
Wilson's disease   AR; excess copper; cystic degeneration of putamen/globus pallidus  
🗑
Vitamin B12 deficiency   posterior column (↓ proprioception, vibration); lateral corticospinal tract (UMN)  
🗑
Alcohol   Wernicke-Korsakoff syndrome, cerebellar atrophy, central pontine myelinolysis  
🗑
Wernicke encephalopathy   thiamine deficiency; IV with glucose can prompt acute attack  
🗑
Wernicke encephalopathy   mammillary body hemorrhage (ring hemorrhages)  
🗑
S/S   confusion, ataxia, nystagmus, ophthalmoplegia  
🗑
Korsakoff's psychosis   limbic system; antegrade and retrograde memory deficits  
🗑
Acute intermittent porphyria (AIP)   AD; deficiency uroporphyrinogen synthase; ↑ porphobilinogen  
🗑
S/S   drug induced (alcohol, barbiturates); abdominal pain ("bellyful of scars"); dementia  
🗑
Window sill test   urine in AIP colorless; turns port wine color with exposure to light (porphobilin)  
🗑
Rx   heme infusions (inhibits δ-aminolevulinic acid synthetase)  
🗑
Adult brain tumors   70% supratentorial; frontal lobe MC site  
🗑
Childhood brain tumors   70% infratentorial; cerebellum MC site  
🗑
Adult brain tumors (descending order)   GBM, meningioma, acoustic neuroma  
🗑
GBM   high grade astrocytoma; hemorrhage and necrosis; may cross corpus callosum  
🗑
Meningioma   female dominant; arise from arachnoid granulations; psammoma bodies; seizures  
🗑
Acoustic neuroma   schwannoma of the VIIIth nerve; tinnitus; sensorineural hearing loss; neurofibromatosis  
🗑
Childhood brain tumors   astrocytoma cerebellum (MC), medulloblastoma  
🗑
Astrocytoma   MC primary brain tumor; frontal lobe MC site in adult; cerebellum MC site in child  
🗑
Medulloblastoma   malignant tumor cerebellum; invades fourth ventricle  
🗑
Ependymoma   arises in 4th ventricle in children and cauda equina in adults  
🗑
Oligodendroglioma   frontal lobe tumor with dystrophic calcification  
🗑
CNS lymphomas   metastasis MCC; primary CNS lymphoma associated with EBV in AIDS  
🗑
Metastasis   MC brain malignancy; lung cancer MC site of origin; junction gray and white matter  
🗑
Schwannoma   benign tumor Schwann cell; MC peripheral nerve tumor; alternating dark and light areas  
🗑
AIDS dementia   due to HIV; multinucleated microglial cells  
🗑
CMV retinitis   MCC of blindness in AIDS; Rx. ganciclovir (foscarnet if unsuccessful)  
🗑
Peripheral neuropathy   myelin destruction (sensory; paresthesias); axon destruction (muscle atrophy)  
🗑
Peripheral neuropathy   DM MCC; thiamine/pyridoxine deficiency; vinca alkaloids (vincristine)  
🗑
Guillain-Barre syndrome   MCC autoimmune demyelination of peripheral and spinal nerves  
🗑
Risk factors   M. pneumoniae, influenza vaccine, Campylobacter jejuni  
🗑
S/S   ascending paralysis; CSF increased protein, lymphocytes; Rx. plasmapheresis  
🗑
Charcot-Marie-Tooth   AD; common peroneal nerve palsy; inverted bottle appearance  
🗑
Idiopathic Bell's palsy   facial muscle paralysis due to inflammation of cranial nerve VII  
🗑
Lyme disease   facial nerve MC cranial nerve involved; bilateral Bell's palsy  
🗑
Bacterial conjunctivitis   Staphylococcus aureus  
🗑
Viral conjunctivitis   adenovirus MC; HSV-1 (dendritic ulcers)  
🗑
Sudden loss of vision   amaurosis fugax, central retinal artery or vein occlusion  
🗑
Uveitis   inflammation of iris, choroid, ciliary body; blurry vision; ankylosing spondylitis, sarcoidosis  
🗑
Optic neuritis   multiple sclerosis MCC; methyl alcohol poisoning  
🗑
Glaucoma   increased intraocular pressure; fluid cannot exit canal of Schlemm; causes optic atrophy  
🗑
Optic atrophy   blindness; pale disc; glaucoma, optic neuritis  
🗑
Macular degeneration   MCC permanent visual loss in elderly  
🗑
Meniere's disease   increased endolymph; tinnitus, vertigo, sensorineural hearing loss  
🗑
Presbycusis   MCC sensorineural hearing loss in elderly  
🗑
Otosclerosis   MCC conductive hearing loss in elderly; fusion of ear ossicles  
🗑
Impacted wax in outer ear canal   conduction hearing loss  
🗑
Weber test lateralizes to left ear, bone>air conduction (Rinne test)   conduction loss left ear  
🗑
Weber test lateralizes to left ear, air>bone conduction both ears   sensorineural hearing loss right ear  
🗑
Otitis media   MCC conduction hearing loss in children; S. pneumoniae MCC  
🗑
Malignant external otitis in diabetic   Pseudomonas aeruginosa  
🗑
T cells   60-70% total lymphocyte count; ↓ AIDS, DiGeorge, adenine deaminase deficiency  
🗑
B cells   10-20% total lymphocyte count; ↓ Bruton's, adenine deaminase deficiency  
🗑
Antigen presenting cells   B cells, macrophages, dendritic cells  
🗑
Langerhan's cells   antigen presenting cell in skin  
🗑
Major histocompatibility complex   chromosome 6; HLA genes for self-identity  
🗑
Class I proteins   recognized by CD8 T cells and NK cells  
🗑
Class II proteins   recognized by CD4 TH cells  
🗑
Type I reactions   IgE antibodies; mast cells; wheal and flare with bee sting  
🗑
Type II reactions   antibody-mediated; Goodpasture's syndrome, rheumatic fever  
🗑
Type III reactions   immune complex-mediated; SLE glomerulonephritis  
🗑
Type IV reactions   cellular immunity; granuloma, positive PPD  
🗑
Delayed reaction hypersensitivity reactions   CD4 TH cells and macrophages  
🗑
Cytotoxic reactions   CD8 T cells; killing viral infected cells and neoplastic cells  
🗑
Graft viability   ABO compatibility most important; HLA match  
🗑
Fetus   allograft that is not rejected  
🗑
Hyperacute rejection   type II hypersensitivity; ABO incompatibility or anti-HLA antibodies  
🗑
Acute rejection   predominately cell-mediated reaction; MC rejection  
🗑
Graft vs. host reaction   jaundice, rash, bloody diarrhea  
🗑
IgA immunodeficiency   MC hereditary immunodeficiency; giardiasis, allergies  
🗑
Bruton's agammaglobulinemia   XR; pre B cannot develop into B cells; S. pneumoniae infections  
🗑
DiGeorge syndrome   failure 3rd/4th pharyngeal pouches to develop; T cell deficiency; absent thymus  
🗑
S/S DiGeorge syndrome   absent thymic shadow; Candida, Pneumocystis infections; hypoparathyroidism  
🗑
Adenine deaminase deficiency   AR; combined B and T cell deficiency; gene therapy  
🗑
Wiskott Aldrich syndrome   XR; combined B and T cell deficiency; eczema, thrombocytopenia  
🗑
AIDS   MC acquired immunodeficiency HIV  
🗑
HIV transmission   MC sexually-transmitted; anal intercourse in homosexuals MCC  
🗑
HIV transmission in health care workers   accidental needle stick from HIV positive patient  
🗑
Follicular dendritic cell   reservoir for HIV in lymph nodes in latent phase  
🗑
AIDS   HIV positive plus CD4, TH cell ≤200 cells/μL or AIDS-defining condition  
🗑
Pneumocystis carinii pneumonia   MC AIDS-defining disorder  
🗑
Screening test for HIV   ELISA test; detects anti-gp120  
🗑
Confirmatory test for HIV   Western blot  
🗑
HIV test with two peaks   p24 antigen; positive prior to seroconversion and when AIDS is diagnosed  
🗑
MC cancer in AIDS   Kaposi sarcoma  
🗑
MC infections CD4 TH <100 cells/μL   CMV, toxoplasmosis, M. avium-intracellulare  
🗑
Hereditary angioedema   deficiency C1 esterase inhibitor; ↓ C2, C4, normal C3  
🗑
Osmosis   H2O shift between ECF and ICF; controlled by serum Na+ and glucose  
🗑
Serum Na+ ~ TBNa+/TBW   decreased TBNa+ dehydration; increased TBNa+ pitting edema  
🗑
Isotonic loss   serum Na+ normal; adult diarrhea, loss whole blood; Rx with 0.9% saline  
🗑
Isotonic gain   serum Na+ normal; Rx with salt and H2O restriction  
🗑
Hyponatremia   ICF expanded; central pontine myelinolysis with rapid IV correction  
🗑
Hyponatremia hypotonic gain pure water   inappropriate ADH syndrome  
🗑
Hyponatremia hypotonic gain TBNa+ and TBW   pitting edema; cirrhosis, RHF  
🗑
Hyponatremia hypertonic loss TBNa+   dehydration; loop diuretic, Addison's, 11-hydroxylase deficiency  
🗑
Hypertonic state   hypernatremia or hyperglycemia; ICF contraction  
🗑
Hypernatremia hypertonic gain TBNa+   pitting edema; sodium bicarbonate  
🗑
Hypernatremia hypotonic loss water   diabetes insipidus  
🗑
Hypernatremia hypotonic loss TBNa+ and TBW   osmotic diuresis, sweat, baby diarrhea  
🗑
Acidosis   potential for hyperkalemia (shift out of ICF)  
🗑
Alkalosis   potential for hypokalemia (shift into ICF)  
🗑
Hypokalemia   loop and thiazide diuretics MCC; alkalosis, albuterol/insulin; U wave  
🗑
Hyperkalemia   renal failure MCC; acidosis, ß-blocker, digitalis toxicity; peaked T wave  
🗑
Rx hyperkalemia   calcium gluconate → insulin with glucose → loop diuretic  
🗑
Respiratory acidosis   PaCO2 >45 mm Hg; compensation metabolic alkalosis  
🗑
Respiratory acidosis   chronic bronchitis, ARDS, barbiturate poisoning, paralysis diaphragms  
🗑
Respiratory alkalosis   PaCO2 <33 mm Hg; compensation metabolic acidosis  
🗑
Respiratory alkalosis   pulmonary embolus, anxiety, early bronchial asthma, restrictive lung disease  
🗑
Metabolic alkalosis   HCO3- >28 mEq/L; compensation respiratory acidosis  
🗑
Metabolic alkalosis   loop/thiazide diuretics, vomiting, primary aldosteronism  
🗑
Metabolic acidosis   HCO3- <2 mEq/L; compensation respiratory alkalosis  
🗑
↑ AG metabolic acidosis   add anions of acid to extracellular fluid  
🗑
↑ AG metabolic acidosis   lactate, AcAc, ß-OHB, salicylate, oxalate (ethylene glycol), formate (methyl alcohol), phosphate/sulfate (renal failure)  
🗑
Ethylene glycol, methyl alcohol   compete with alcohol for alcohol dehydrogenase  
🗑
Ethylene glycol poisoning   antifreeze; converted to oxalic acid; renal failure  
🗑
Methyl alcohol poisoning   window wiper fluid; converted to formic acid; blindness  
🗑
Normal AG metabolic acidosis   lose HCO3-; e.g., diarrhea, proximal/distal renal tubular acidosis  
🗑
AFP   increased in open neural tube defects; decreased in Down syndrome  
🗑
PCR   uses DNA polymerase  
🗑
Barr body   inactive X chromosome on nuclear membrane; 1 Barr body in females  
🗑
Missense mutation   point mutation with different amino acid; sickle cell trait/disease, Marfan  
🗑
Nonsense mutation   point mutation producing stop codon; ß-thalassemia major  
🗑
Frameshift mutation   insertion or deletion nucleotides alters reading frame; Tay-Sachs  
🗑
Trinucleotide repeat   disease worse in future generations (anticipation)  
🗑
Trinucleotide repeat disorders   fragile X (XR), Huntington's (AD), myotonic dystrophy (AD)  
🗑
Nondisjunction   meiosis; unequal numbers of chromosomes  
🗑
Robertsonian translocation   Down syndrome with 46 chromosomes  
🗑
Microdeletion syndrome   genomic imprinting; chromosome 15  
🗑
Paternal microdeletion   Prader-Willi; obese, mental retardation  
🗑
Maternal microdeletion   Angelman's syndrome; happy puppy syndrome, mental retardation  
🗑
Advanced maternal age   increased risk for trisomies  
🗑
Down syndrome   trisomy 21; leading cause mental retardation  
🗑
S/S   slanted eyes; simian crease; endocardial cushion defect; Alzheimer's  
🗑
Turner's syndrome   XO; no Barr bodies; short stature and primary amenorrhea; streak ovaries  
🗑
Klinefelter's syndrome   XXY; 1 Barr body; female secondary sex characteristics  
🗑
AR   homozygous (aa) for disease; heterozygotes (Aa) asymptomatic  
🗑
AR   most inborn errors metabolism, sickle cell, cystic fibrosis, hemochromatosis, Wilson's  
🗑
AD   homozygote (aa) or heterozygote (Aa) express disease  
🗑
AD   spherocytosis, Marfan's syndrome, neurofibromatosis, von Willebrand, familial polyposis, polycystic kidney  
🗑
AD   delayed manifestation; penetrance; variable expressivity  
🗑
XR   male transmits to all daughters; female carrier transmits to 50% of sons  
🗑
XR   G6PD deficiency, Bruton, Lesch-Nyhan, testicular feminization, fragile X, hemophilia A/B  
🗑
Fragile X   mental retardation; macroorchidism at puberty; trinucleotide repeat  
🗑
Lesch Nyhan   XR; deficiency HGPRT; hyperuricemia; mental retardation  
🗑
Multifactorial inheritance   gout, type 2 diabetes, essential hypertension  
🗑
Mitochondrial DNA disorder   maternal transmission to all children; no paternal transmission  
🗑
Y chromosome   determines genetic sex  
🗑
Testosterone   develops seminal vesicles, epididymis, vas deferens  
🗑
Dihydrotestosterone   develops prostate and male external genitalia  
🗑
Male pseudohermaphrodite   genetic male; phenotypically female  
🗑
Female pseudohermaphrodite   genetic female; phenotypically male  
🗑
Testicular feminization   XR; deficient androgen receptors; MCC male pseudohermaphrodite  
🗑
21-Hydroxylase deficiency   ↑ 17 KS, ↓ 17 OH, lose salt, hypotension; female pseudohermaphrodite  
🗑
11-Hydroxylase deficiency   ↑ 17 KS, ↑ 17 OH, retain salt, hypertension; female pseudohermaphrodite  
🗑
17-Hydroxylase deficiency   ↓ 17 KS, ↓ 17 OH, retain salt, hypertension; male pseudohermaphrodite  
🗑
Calculate prevalence   carrier rate 1:30; couples at risk  
🗑
Calculate carrier rate   1:3600; 3600 /4 = 900; √900) = 1:30  
🗑
Malformation   intrinsic problem with morphogenesis  
🗑
HOX gene   involved in embryogenesis  
🗑
Alcohol   MCC of malformations; mental retardation; atrial septal defect  
🗑
Isotretinoin acid   craniofacial and cardiac defects  
🗑
Female with cystic acne needs Rx with retinoic acid   do pregnancy test before placing female on drug  
🗑
DES   problem with mullerian development; clear cell carcinoma of vagina  
🗑
Thalidomide   limb abnormalities  
🗑
Vertical transmission   transplacental (MC), delivery, breast feeding  
🗑
Congenital CMV   MC congenital infection; periventricular calcification; culture urine  
🗑
Congenital toxoplasmosis   basal ganglia calcification; blindness; avoid cat litter in pregnancy  
🗑
Congenital rubella   sensorineural hearing loss (MC); cataracts  
🗑
Congenital syphilis   transplacental after 5-6 months; saddle nose, rhagades, blindness, deformed teeth  
🗑
Congenital herpes   contracted during delivery; encephalitis  
🗑
Deformation   extrinsic problem in fetal development; oligohydramnios causing Potter's facies  
🗑
Tobacco   leading cause premature death and cancer in United States  
🗑
Nicotine   most addictive substance; attaches to nicotinic cholinergic receptors  
🗑
Tobacco induced cancers   lung, oropharynx, larynx, pancreas, kidney, bladder  
🗑
Alcohol   CNS depressant (cortex, limbic system); legally drunk 80-100 mg/dL  
🗑
Alcohol   induces SER hyperplasia; increases alcohol metabolism  
🗑
Alcohol MCC of   folate/thiamine deficiency; sideroblastic anemia; liver fatty change; pancreatitis  
🗑
Alcohol   hypoglycemia; lactic/ketoacidosis; ↑ triglyceride; AST>ALT; ↑ GGT  
🗑
Ketoacidosis in alcoholic   ß-hydroxybutyric acid  
🗑
Heroin   poppy plant; non-cardiogenic pulmonary edema; focal segmental glomerulosclerosis  
🗑
MPTP   meperidine derivative; produces parkinsonism  
🗑
Cocaine   blocks uptake of dopamine/norepinephrine; mydriasis; AMI, CNS infarction  
🗑
Marijuana   tetrahydrocannabinol (THC) binds basal ganglia receptors; delayed reaction time; red conjunctiva  
🗑
Intravenous drug abuse   HBV hepatitis MC systemic disease  
🗑
Acetaminophen toxicity   damage by FR acetaminophen; liver cell necrosis; renal papillary necrosis  
🗑
Rx acetaminophen toxicity   N-acetylcysteine (increases synthesis of glutathione)  
🗑
Salicylate toxicity   metabolic acidosis + respiratory alkalosis; hyperthermia; tinnitus, vertigo  
🗑
Estrogen risks   thromboembolism; cholestasis; endometrial/breast cancer  
🗑
Oral contraceptives   cholestasis, thrombosis, folate deficiency, hypertension, hepatic adenoma  
🗑
Hemolytic anemia   penicillin, methyldopa, quinidine  
🗑
Aplastic anemia   benzene, chloramphenicol  
🗑
Qualitative platelet dysfunction   NSAIDs  
🗑
Thrombocytopenia   heparin, quinidine  
🗑
Macrocytic anemia   methotrexate, 5-fluorouracil, phenytoin, OC, alcohol  
🗑
Congestive cardiomyopathy   doxorubicin, daunorubicin  
🗑
Interstitial fibrosis   bleomycin, methotrexate  
🗑
Hemorrhagic gastritis   iron toxicity, NSAIDs  
🗑
Liver necrosis   acetaminophen, isoniazid, salicylates, halothane, isotretinoin acid  
🗑
Cholestasis   anabolic steroids, OC  
🗑
Fatty change in liver   amiodarone, tetracycline, alcohol  
🗑
Photosensitive rash   tetracycline  
🗑
SLE   procainamide, hydralazine  
🗑
Isopropyl alcohol   ↑ acetone; CNS dysfunction  
🗑
Lead   microcytic anemia, nephrotoxic ATN (proximal tubule), gout, encephalopathy, neuropathy  
🗑
Mercury   fish (tuna, salmon); nephrotoxic ATN; constricted visual fields  
🗑
Organophosphates   blocks acetylcholine esterase; miosis; paralysis; Rx. atropine, pralidoxime  
🗑
Polyvinyl chloride   plastic pipes; angiosarcoma of liver  
🗑
Scorpion sting   paralysis, hypertension, pancreatitis  
🗑
Crotaline bite   rattlesnakes, water moccasin, copperhead; DIC; serum sickness  
🗑
Coral snake bite   neurotoxin; binds to presynaptic nerve terminals and acetylcholine receptors  
🗑
Contact gunshot wound   soot + gunpowder (fouling)  
🗑
Intermediate gunshot wound   powder tattooing  
🗑
Distant gunshot wound   no powder tattooing; exit wound larger than entrance  
🗑
Motor vehicle accidents   leading cause accidental death between 1-39 yrs of age  
🗑
Burns   Pseudomonas aeruginosa sepsis MC COD  
🗑
First degree burn   painful; complete healing  
🗑
Second degree burn   painful; blister; complete healing  
🗑
Third degree burn   painless; scarring  
🗑
Frostbite   painless; ice crystallization in cells  
🗑
Electrical injury   AC worse than DC; decreasing resistance (wet skin) increases current  
🗑
House fires   carbon monoxide and cyanide poisoning  
🗑
Heat exhaustion   fever and sweating  
🗑
Heat stroke   fever and anhydrosis  
🗑
Near drowning   survival following asphyxia due to submersion  
🗑
Wet drowning   initial laryngospasm then relaxation and water into lungs  
🗑
Dry drowning   intense laryngospasm without aspiration  
🗑
Cold water drowning   shunts blood from periphery to central core  
🗑
Drowning   hypoxemia key COD  
🗑
Acute mountain sickness   headache MC; non-cardiogenic pulmonary edema (immediate descent)  
🗑
High altitude   normal %O2; decreased barometric pressure; respiratory alkalosis; ↑ 2, 3 BPG  
🗑
Ionizing radiation   DNA most susceptible protein  
🗑
Ionizing radiation   lymphoid tissue most radiosensitive; bone least radiosensitive  
🗑
Ionizing radiation cancers   leukemia (most common); thyroid cancer; osteogenic sarcoma  
🗑
UVB-related cancers   basal cell carcinoma (most common); squamous cancer; melanoma  
🗑
Carbohydrates   digestion begins in mouth  
🗑
Fats   digestion begins in small intestine  
🗑
Essential fatty acid deficiency   dermatitis, hair loss, poor wound healing  
🗑
Proteins   digestion begins in stomach  
🗑
Kwashiorkor   ↓ protein intake; ↓ visceral protein; ↓ albumin (pitting edema); fatty liver  
🗑
Marasmus   total calorie deprivation; ↓ somatic protein; broomstick extremities  
🗑
Anorexia nervosa   starvation; secondary amenorrhea (↓ GnRH); osteoporosis; ventricular MC COD  
🗑
Bulimia nervosa   binging with vomiting; hypokalemic metabolic alkalosis; ventricular MC COD  
🗑
Body mass index (BMI)   weight in kg/height in m2  
🗑
Obesity   hypertension (MC), cholecystitis, osteoarthritis, type 2 DM, endometrial/breast cancer  
🗑
Leptin   obesity gene product released from adipose; maintains energy balance  
🗑
All-trans retinoic acid   Rx acute promyelocytic leukemia; matures blasts to neutrophils  
🗑
Vitamin A   maintain visual purple, prevent squamous metaplasia, growth  
🗑
Vitamin A deficiency   night blindness; blindness; squamous metaplasia  
🗑
Vitamin A toxicity   ↑ intracerebral pressure; papilledema; hepatic necrosis  
🗑
Vitamin D   maintain ionized Ca2+; mineralization of bone  
🗑
Vitamin D metabolism   skin photoconversion or reabsorb in gut → 1st hydroxylation liver → 2nd hydroxylation proximal tubule (1-α-hydroxylase) Vitamin D deficiency  
🗑
Causes   renal failure MCC; malabsorption; liver disease; ↓ sunlight  
🗑
Lab   ↓ Ca2+, ↓ phosphate (malabsorption), ↑ phosphate renal failure, ↑ PTH  
🗑
Hypervitaminosis D   ↑ Ca2+, renal stones  
🗑
Vitamin E   prevents FR damage of cell membrane  
🗑
Vitamin E deficiency   hemolytic anemia; posterior column/spinocerebellar tract degeneration  
🗑
Vitamin E toxicity   ↓ synthesis vitamin K-dependent procoagulation factors; anticoagulated  
🗑
Vitamin K   γ-carboxylates vitamin K-dependent factors  
🗑
Vitamin K deficiency   ↓ epoxide reductase activity (↓ function vitamin K); hemorrhagic diathesis; ↑ PT  
🗑
Warfarin   inhibits epoxide reductase  
🗑
Causes vitamin K deficiency   antibiotics MC, newborn, malabsorption, warfarin  
🗑
Thiamine functions   transketolase; dehydrogenase reactions (NADH for ATP synthesis)  
🗑
Example of dehydrogenase reaction   pyruvate → acetyl CoA; pyruvate dehydrogenase  
🗑
Thiamine deficiency   alcohol MCC; ↓ ATP synthesis  
🗑
S/S   dry beriberi - Wernicke's, Korsakoff's, peripheral neuropathy; wet beriberi - cardiomyopathy  
🗑
Niacin   oxidation-reduction reactions; NAD; NADP  
🗑
Niacin deficiency   pellagra; dermatitis, diarrhea, dementia  
🗑
Tryptophan   synthesis niacin, serotonin  
🗑
Tryptophan deficiency   Hartnup's disease (↓ reabsorption neutral amino acids); carcinoid syndrome  
🗑
S/S niacin deficiency   diarrhea, dermatitis, dementia  
🗑
Corn   deficient in niacin and tryptophan  
🗑
Pyridoxine   heme synthesis, transamination, neurotransmitter synthesis  
🗑
Cause   taking isoniazid  
🗑
Pyridoxine (B6) deficiency   sideroblastic anemia; convulsions; peripheral neuropathy  
🗑
Vitamin B12/folate   DNA maturation, odd chain fatty acid metabolism (propionyl CoA)  
🗑
Vitamin B12/folate deficiency   macrocytic anemia  
🗑
Biotin   carboxylase reactions (pyruvate → oxaloacetate)  
🗑
Cause   eating raw eggs (avidin binds vitamin)  
🗑
S/S   alopecia, dermatitis  
🗑
Vitamin C   antioxidant, reduce ferric iron, hydroxylation proline/lysine, dopamine → norepinephrine  
🗑
Vitamin C deficiency   scurvy; hemorrhagic diathesis; poor wound healing  
🗑
Alkalotic state   lowers ionized Ca2+ producing tetany; total Ca2+ normal  
🗑
Hypoalbuminemia   lowers total Ca2+; no tetany  
🗑
Hypophosphatemia   decreased ATP; myoglobinuria  
🗑
Hypomagnesemia   causes hypocalcemia by inhibiting PTH synthesis/release  
🗑
Zinc deficiency   poor wound healing; dysgeusia (cannot taste); anosmia; perioral rash  
🗑
Copper deficiency   iron deficiency; poor wound healing (cofactor lysyl oxidase); aortic dissection  
🗑
Iodine deficiency   produces goiter and hypothyroidism  
🗑
Chromium deficiency   glucose intolerance  
🗑
Selenium   antioxidant that neutralizes peroxide  
🗑
Fluoride deficiency   dental caries  
🗑


   

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