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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 |