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USMLE Rapid Review
Term | Definition |
---|---|
Budd-Chiari syndrome | Abdominal pain, ascites, hepatomegaly |
Familial hypercholesterolemia | Achilles tendon xanthoma |
Waterhouse-Friderichsen syndrome | Adrenal hemorrhage, hypotension, DIC |
ACL injury | Anterior “drawer sign” |
Marfan syndrome | Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints |
2° to erythropoietin injection | Athlete with polycythemia |
Pott disease | Back pain, fever, night sweats, weight loss |
Sarcoidosis | Bilateral hilar adenopathy, uveitis |
Osteogenesis imperfecta | Blue sclera |
Burton line | Bluish line on gingiva |
Paget disease of bone | Bone pain, bone enlargement, arthritis |
Aortic regurgitation | Bounding pulses, diastolic heart murmur, head bobbing |
Systemic lupus erythematosus | “Butterfly” facial rash and Raynaud phenomenon in a young female |
Neurofibromatosis type I | Café-au-lait spots, Lisch nodules (iris hamartoma) |
McCune-Albright syndrome | Café-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine abnormalities |
Duchenne muscular dystrophy | Calf pseudohypertrophy |
Tay-Sachs | “Cherry-red spots” on macula |
Angina | Chest pain on exertion |
Dressler syndrome | Chest pain, pericardial effusion/friction rub, persistent fever following MI |
Gowers sign | Child uses arms to stand up from squat |
“Slapped cheeks” | Child with fever later develops red rash on face that spreads to body |
Huntington disease | Chorea, dementia, caudate degeneration |
McArdle disease | Chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria |
Hypothyroidism | Cold intolerance |
Internuclear ophthalmoplegia | Conjugate lateral gaze palsy, horizontal diplopia |
PDA | Continuous “machine-like” heart murmur |
Myxedema | Cutaneous/dermal edema due to connective tissue deposition |
Kaposi sarcoma | Dark purple skin/mouth nodules in a patient with AIDS |
Kussmaul respirations | Deep, labored breathing/hyperventilation |
Pellagra | Dermatitis, dementia, diarrhea |
Wet beriberi | Dilated cardiomyopathy, edema, alcoholism or malnutrition |
Pasteurella multocida | Dog or cat bite resulting in infection |
Sjögren syndrome | Dry eyes, dry mouth, arthritis |
Plummer-Vinson syndrome | Dysphagia (esophageal webs), glossitis, iron deficiency anemia |
Ehlers-Danlos syndrome | Elastic skin, hypermobility of joints |
Virchow node | Enlarged, hard left supraclavicular node |
Mycosis fungoides or Sézary syndrome | Erythroderma, lymphadenopathy, hepatosplenomegaly, atypical T cells |
Chvostek sign | Facial muscle spasm upon tapping |
Cholelithiasis | Fat, female, forty, and fertile |
Jarisch-Herxheimer reaction | Fever, chills, headache, myalgia following antibiotic treatment for syphilis |
Measles | Fever, cough, conjunctivitis, coryza, diffuse rash |
B symptoms of lymphoma | Fever, night sweats, weight loss |
Peyronie disease | Fibrous plaques in soft tissue of penis |
Lesch-Nyhan syndrome | Gout, intellectual disability, self-mutilating behavior in a boy |
Kayser-Fleischer rings | Green-yellow rings around peripheral cornea |
Peutz-Jeghers syndrome | Hamartomatous GI polyps, hyperpigmentation of mouth/feet/hands |
Gaucher disease | Hepatosplenomegaly, osteoporosis, neurologic symptoms |
Alport syndrome | Hereditary nephritis, sensorineural hearing loss, cataracts |
Klüver-Bucy syndrome | Hyperphagia, hypersexuality, hyperorality, hyperdocility |
UMN damage | Hyperreflexia, hypertonia, Babinski sign present |
LMN damage | Hyporeflexia, hypotonia, atrophy, fasciculations |
“Blue bloater” (chronic bronchitis) | Hypoxemia, polycythemia, hypercapnia |
Patau syndrome (trisomy 13) | Infant with cleft lip/palate, microcephaly or holoprosencephaly, polydactyly, cutis aplasia |
Niemann-Pick disease | Infant with failure to thrive, hepatosplenomegaly, and neurodegeneration |
Cori disease or Von Gierke disease | Infant with hypoglycemia, failure to thrive, and hepatomegaly |
Edwards syndrome (trisomy 18) | Infant with microcephaly, rocker-bottom feet, clenched hands, and structural heart defect |
Courvoisier sign | Jaundice, palpable distended non-tender gallbladder |
Lyme disease: Borrelia | Large rash with bull’s-eye appearance |
Epidural hematoma | Lucid interval after traumatic brain injury |
Bruton disease | Male child, recurrent infections, no mature B cells |
Glanzmann thrombasthenia | Mucosal bleeding and prolonged bleeding time |
Beck triad of cardiac tamponade | Muffled heart sounds, distended neck veins, hypotension |
Gardner syndrome | Multiple colon polyps, osteomas/soft tissue tumors, impacted/supernumerary teeth |
Pompe disease | Myopathy (infantile hypertrophic cardiomyopathy), exercise intolerance |
Erb-Duchenne palsy | Neonate with arm paralysis following difficult birth |
Sheehan syndrome | No lactation postpartum, absent menstruation, cold intolerance |
Multiple sclerosis | Nystagmus, intention tremor, scanning speech, bilateral internuclear ophthalmoplegia |
Cheyne-Stokes respirations | Oscillating slow/fast breathing |
Cold agglutinin disease | Painful blue fingers/toes, hemolytic anemia |
Raynaud phenomenon | Painful, pale, cold fingers/toes |
Osler nodes | Painful, raised red lesions on pad of fingers/toes |
Janeway lesions | Painless erythematous lesions on palms and soles |
Cancer of the pancreatic head obstructing bile duct | Painless jaundice |
Henoch-Schönlein purpura | Palpable purpura on buttocks/legs, joint pain, abdominal pain (child), hematuria |
MEN 1 | Pancreatic, pituitary, parathyroid tumors |
Nephrotic syndrome | Periorbital and/or peripheral edema, proteinuria, hypoalbuminemia, hypercholesterolemia |
“Pink puffer” (emphysema) | Pink complexion, dyspnea, hyperventilation |
Fanconi syndrome | Polyuria, renal tubular acidosis type II, growth failure, electrolyte imbalances, hypophosphatemic rickets |
Lichen planus | Pruritic, purple, polygonal planar papules and plaques (6 P’s) |
Horner syndrome | Ptosis, miosis, anhidrosis |
Argyll Robertson pupil | Pupil accommodates but doesn’t react |
Guillain-Barré syndrome | Rapidly progressive leg weakness that ascends following GI/upper respiratory infection |
Coxsackie A, 2° syphilis, Rocky Mountain spotted fever | Rash on palms and soles |
Hyper-IgE syndrome | Recurrent colds, unusual eczema, high serum IgE |
Klebsiella pneumoniae | Red “currant jelly” sputum in alcoholic or diabetic patients |
Acute mesenteric ischemia (adults), intussusception (infants) | Red “currant jelly” stools |
Paget disease of the breast | Red, itchy, swollen rash of nipple/areola |
Paroxysmal nocturnal hemoglobinuria | Red urine in the morning, fragile RBCs |
von Hippel-Lindau disease | Renal cell carcinoma (bilateral), hemangioblastomas, angiomatosis, pheochromocytoma |
Parkinson disease | Resting tremor, rigidity, akinesia, postural instability |
Roth spots | Retinal hemorrhages with pale centers |
Crigler-Najjar syndrome | Severe jaundice in neonate |
Rovsing sign | Severe RLQ pain with palpation of LLQ |
McBurney sign | Severe RLQ pain with rebound tenderness |
Fanconi anemia | Short stature, incidence of tumors/leukemia, aplastic anemia |
Down syndrome | Single palmar crease |
Kartagener syndrome | Situs inversus, chronic sinusitis, bronchiectasis, infertility |
Addison disease | Skin hyperpigmentation, hypotension, fatigue |
Becker muscular dystrophy | Slow, progressive muscle weakness in boys |
Koplik spots | Small, irregular red spots on buccal/lingual mucosa with blue-white centers |
Condylomata lata (2° syphilis) | Smooth, flat, moist, painless white lesions on genitals |
Bacterial endocarditis | Splinter hemorrhages in fingernails |
Scarlet fever, Kawasaki disease, toxic shock syndrome | “Strawberry tongue” |
Turner syndrome | Streak ovaries, congenital heart disease, horseshoe kidney, cystic hygroma at birth, short stature, webbed neck, lymphedema |
Gout/podagra | Sudden swollen/painful big toe joint, tophi |
Scurvy | Swollen gums, mucosal bleeding, poor wound healing, petechiae |
Osteoarthritis | Swollen, hard, painful finger joints |
Aortic valve stenosis | Systolic ejection murmur (crescendo-decrescendo) |
MEN 2A | Thyroid and parathyroid tumors, pheochromocytoma |
MEN 2B | Thyroid tumors, pheochromocytoma, ganglioneuromatosis |
Babinski sign | Toe extension/fanning upon plantar scrape |
Facial nerve (LMN CN VII palsy/Bell's palsy) | Unilateral facial drooping involving forehead |
Reactive arthritis associated with HLA-B27 | Urethritis, conjunctivitis, arthritis in a male |
Hemangioma | Vascular birthmark (port-wine stain) |
Mallory-Weiss syndrome | Vomiting blood following gastroesophageal lacerations |
Whipple disease | Weight loss, diarrhea, arthritis, fever, adenopathy |
Subarachnoid hemorrhage | “Worst headache of my life” |
Scleroderma (CREST) | Anticentromere antibodies |
Pemphigus vulgaris | Antidesmoglein (epithelial) antibodies |
Goodpasture syndrome | Anti–glomerular basement membrane antibodies |
Drug-induced SLE | Antihistone antibodies |
Rheumatoid arthritis | Anti-IgG antibodies |
1° biliary cirrhosis | Antimitochondrial antibodies (AMAs) |
Microscopic polyangiitis and Churg-Strauss syndrome | Antineutrophil cytoplasmic antibodies (ANCAs) |
SLE (type III hypersensitivity) | Antinuclear antibodies (ANAs: anti-Smith and anti-dsDNA) |
Idiopathic thrombocytopenic purpura | Antiplatelet antibodies |
Diffuse systemic scleroderma | Anti-topoisomerase antibodies |
Celiac disease | Anti-transglutaminase/anti-gliadin/anti-endomysial antibodies |
Colorectal cancer | “Apple core” lesion on abdominal x-ray |
Auer rods | Azurophilic peroxidase granular inclusions in granulocytesand myeloblasts |
Sensitive: Streptococcus pyogenes (group A); resistant: Streptococcus agalactiae (group B) | Bacitracin response |
Ankylosing spondylitis | “Bamboo spine” on x-ray |
Howell-Jolly bodies | Basophilic nuclear remnants in RBCs |
Lead poisoning or sideroblastic anemia | Basophilic stippling of RBCs |
Subarachnoid hemorrhage | Bloody tap on LP |
Tetralogy of Fallot, RVH | “Boot-shaped” heart on x-ray |
Actinomyces israelii | Branching gram-positive rods with sulfur granules |
Pancoast tumor | Bronchogenic apical lung tumor on imaging |
Hyperparathyroidism or osteitis fibrosa cystica | “Brown” tumor of bone |
Chagas disease | Cardiomegaly with apical atrophy |
Rapidly progressive crescentic glomerulonephritis | Cellular crescents in Bowman capsule |
Endometriosis | “Chocolate cyst” of ovary |
Homer-Wright rosettes | Circular grouping of dark tumor cells surrounding pale neurofibrils |
Cystic fibrosis | Colonies of mucoid Pseudomonas in lungs |
Down syndrome or other chromosomal abnormality | Decrease in AFP in amniotic fluid/maternal serum |
Tabes dorsalis | Degeneration of dorsal column nerves |
Parkinson disease | Depigmentation of neurons in substantia nigra |
Curschmann spirals | Desquamated epithelium casts in sputum |
Call-Exner bodies | Disarrayed granulosa cells in eosinophilic fluid |
Koilocytes | Dysplastic squamous cervical cells with nuclear enlargement and hyperchromasia |
“Owl eye” appearance of CMV | Enlarged cells with intranuclear inclusion bodies |
“Orphan Annie” eyes nuclei | Enlarged thyroid cells with ground-glass nuclei |
Mallory body (alcoholic liver disease) | Eosinophilic cytoplasmic inclusion in liver cell |
Lewy body (Parkinson disease) | Eosinophilic cytoplasmic inclusion in nerve cell |
Councilman body | Eosinophilic globule in liver |
Negri bodies of rabies | Eosinophilic inclusion bodies in cytoplasm of hippocampal and cerebellar nerve cells |
Senile plaques (Alzheimer disease) | Extracellular amyloid deposition in gray matter of brain |
Reed-Sternberg cells (Hodgkin lymphoma) | Giant B cells with bilobed nuclei with prominent inclusions (“owl’s eye”) |
Schiller-Duval bodies (yolk sac tumor) | Glomerulus-like structure surrounding vessel in germ cells |
β-thalassemia, sickle cell anemia | “Hair on end” (crew-cut) appearance on x-ray |
Choriocarcinoma, | hCG elevated |
Aschoff bodies (rheumatic fever) | Heart nodules (granulomatous) |
Infectious mononucleosis (EBV) | Heterophile antibodies |
Bronchial asthma | Hexagonal, double-pointed, needle-like crystals in bronchial secretions |
DVT, PE, DIC | High level of d-dimers |
Ghon complex | Hilar lymphadenopathy, peripheral granulomatous lesion in middle or lower lung lobes (can calcify) |
Interstitial pulmonary fibrosis | “Honeycomb lung” on x-ray or CT |
Trousseau syndrome | Hypercoagulability (leading to migrating DVTs and vasculitis) |
Megaloblastic anemia | Hypersegmented neutrophils |
Conn syndrome | Hypertension, hypokalemia, metabolic alkalosis |
Iron deficiency anemia, lead poisoning, thalassemia | Hypochromic, microcytic anemia |
Dating error, anencephaly, spina bifida (neural tube defects) | Increased AFP in amniotic fluid/maternal serum |
Gout, Lesch-Nyhan syndrome, tumor lysis syndrome, loop and thiazide diuretics | Increased uric acid levels |
Cowdry type A bodies (HSV or CMV) | Intranuclear eosinophilic droplet-like bodies |
Ferruginous bodies | Iron-containing nodules in alveolar septum |
Squamous cell carcinoma | Keratin pearls on a skin biopsy |
Chédiak-Higashi disease | Large lysosomal vesicles in phagocytes, immunodeficiency |
Ulcerative colitis | “Lead pipe” appearance of colon on barium enema x-ray |
Goodpasture syndrome | Linear appearance of IgG deposition on glomerular basement membrane |
Wilson disease | Low serum ceruloplasmin |
Poststreptococcal glomerulonephritis | “Lumpy bumpy” appearance of glomeruli on immunofluorescence |
Multiple myeloma | Lytic (“hole punched”) bone lesions on x-ray |
Fibrocystic change of the breast | Mammary gland (“blue domed”) cyst |
Multiple myeloma (usually IgG or IgA) - Monoclonal gammopathy of undetermined significance - (MGUS consequence of aging) - Waldenström (M protein = IgM) macroglobulinemia - Primary amyloidosis | Monoclonal antibody spike |
“Signet ring” (gastric carcinoma) | Mucin-filled cell with peripheral nucleus |
“String sign” (Crohn disease) | Narrowing of bowel lumen on barium x-ray |
Wegener; PR3-ANCA/c-ANCA and Goodpasture syndrome | Necrotizing vasculitis (lungs) and necrotizing glomerulonephritis |
Gout | Needle-shaped, negatively birefringent crystals |
Kimmelstiel-Wilson nodules | Nodular hyaline deposits in glomeruli |
Sensitive: Staphylococcus epidermidis; resistant: Staphylococcus saprophyticus (No SRES) | Novobiocin response |
Chronic passive congestion of liver due to right heart failure | “Nutmeg” appearance of liver |
Ewing sarcoma | “Onion skin” periosteal reaction |
Sensitive: Streptococcus pneumoniae; resistant: viridans streptococci ( OVRPS) | Optochin response |
Codman triangle on x-ray (osteosarcoma, Ewing sarcoma, pyogenic osteomyelitis) | Periosteum raised from bone, creating triangular area |
Minimal change disease (child with nephrotic syndrome) | Podocyte fusion or “effacement” on electron microscopy |
Eburnation | Polished, “ivory-like” appearance of bone at cartilage erosion |
Neurofibrillary tangles (Alzheimer disease) and Pick bodies (Pick disease) | Protein aggregates in neurons from hyperphosphorylation of tau protein |
Meningiomas, papillary thyroid carcinoma, mesothelioma, papillary serous carcinoma of the endometrium and ovary | Psammoma bodies |
Glioblastoma multiforme | Pseudopalisading tumor cells on brain biopsy |
Acute glomerulonephritis | RBC casts in urine |
Reinke crystals (Leydig cell tumor) | Rectangular, crystal-like, cytoplasmic inclusions in Leydig cells |
Acute toxic/viral renal injury | Renal epithelial casts in urine |
Pseudogout | Rhomboid crystals, positively birefringent |
Coarctation of the aorta | Rib notching |
Toxoplasma gondii, CNS lymphoma | Ring-enhancing brain lesion in AIDS |
Burkitt lymphoma | Sheets of medium-sized lymphoid cells with scattered pale, tingible body–laden macrophages (“starry sky” histology) |
Pick bodies: Pick disease: | Silver-staining spherical aggregation of tau proteins in neurons |
Giant cell tumor of bone | “Soap bubble” in femur or tibia on x-ray |
Membranous glomerulonephritis | “Spikes” on basement membrane, “dome-like” subepithelial deposits |
Rouleaux formation | Stacks of RBCs |
“Clue cells” (Gardnerella vaginalis) | Stippled vaginal epithelial cells |
Birbeck granules (Langerhans cell histiocytosis or histiocytosis X: eosinophilic granuloma) | “Tennis racket”-shaped cytoplasmic organelles (EM) in Langerhans cells |
Lines of Zahn | Thrombi made of white/red layers |
Epiglottitis (Haemophilus influenzae) | “Thumb sign” on lateral x-ray |
Chronic bacterial pyelonephritis | Thyroid-like appearance of kidney |
Membranoproliferative glomerulonephritis | “Tram-track” appearance of capillary loops of glomerular basement membranes on light microscopy |
Fatty liver disease (alcoholic or metabolic syndrome) | Triglyceride accumulation in liver cell vacuoles |
Chronic end-stage renal disease | “Waxy” casts with very low urine flow |
Acute pyelonephritis | WBC casts in urine |
CLL (almost always B cell) | WBCs that look “smudged” |
Lupus nephropathy | “Wire loop” glomerular capillary appearance on light microscopy |
Xanthochromia | Yellowish CSF |