USMLE Step 1 Cards Editable Flashcards
Abdominal pain, ascites, and hepatomegaly
Budd-Chiari syndrome (posthepatic venous thrombosis)
Achilles tendon xanthoma
Familial hypercholesterolemia (dec LDL receptor signaling), AutoDom
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichsen Syndrome (meningococcemia)
Anterior Drawer Sign (positive)
Anterior cruciate ligament injury
Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints
Marfan syndrome (fibrillin defect)
Athlete with polycythemia
Secondary to erythropoietin injection
Back pain, fever, night sweats, weight loss
Pott disease (vertebral TB)
Bilateral hilar adenopathy, uveitis
Sarcoidosis (noncaseating granulomas)
Blue sclera
Osteogenesis imperfecta (type I collagen defect)
Bluish line on gingiva
Burton line (lead poisoning)
Bone pain, bone enlargement, arthritis
Paget disease of bone (increased osteoclastic and osteoblastic activity)
Bounding pulses, diastolic heart murmur, head bobbing
Aortic regurgitation
“Butterfly” facial rash and Raynaud phenomenon in young female
Systemic lupus erythematosus
Cafe-au-lait spots, Lisch nodules (iris hamartoma)
Neurofibromatosis Type I (+ pheochromocytoma, optic gliomas), Chromo 17.
Cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine abnormalities
McCune-Albright Syndrome (mosaic G-protein signaling mutation)
Calf pseudohypertrophy
Muscular dystrophy (most commonly Duchenne): X linked recessive DELETION of dystrophin gene. Presents early. Becker’s presents in teens, DECREASED production.
“Cherry-red spots” on macula
Niemann-Pick (sphingomyelin accumulation, HEPATOSPLENOMEGALY) or Tay-Sachs (ganglioside accumulation, NO HSM) or, central retinal artery occlusion.
Chest pain on exertion
Angina (stable: with moderate exertion; unstable: with minimal exertion)
Chest pain, pericardial effusion/friction rub, persistent fever following MI
Dressler syndrome (autoimmune-mediated post-MI fibrinous pericarditis, 1-12 weeks after acute episode)
Child uses arms to stand up from squat
Gowers Sign (Duchenne muscular dystrophy)
Child with fever later develops red rash on face that spreads to body
“Slapped cheeks” (erythemia infectiosum/fifth disease: parvovarius B19. Aplastic Anemia in sickle cell/hereditary spherocytosis)
Chorea, dementia, caudate degeneration
Huntington disease (autosomal dominant CAG repeat expansion). Disease shows “anticipation”.
Chronic exercise intolerance with myalgia, fatigue, painful cramps, and myoglobulinuria
McArdle Disease (muscle glycogen phosphorylase deficiency)
Cold interolerance
Hypothyroid
Conjugate lateral gaze palsy, horizontal diplopia
Internuclear ophthalmoplegia (damage to MLF [medial longitudinal fasciculus]; bilateral [multiple sclerosis] or unilateral [stroked])
Continuous machine-like heart murmur
PDA (close with indomethacin; open or maintain with misoprostol)
Cutaneous/dermal edema due to connective tissue deposition
Myxedema (caused by hypothyroidism, Graves disease [pretibial])
Dark purple skin/mouth nodules in a patient with AIDS
Kaposi sarcoma, associated with HHV-8
Deep, labored breathing/hyperventilation
Kussmaul respirations (diabete ketoacidosis)
Dermatitis, dementia, diarrhea
Pellagra (niacin [Vitamin B3] deficiency)
Dog or cat bite resulting in infection
Pasteurella multocida (cellulitis at inoculation site)
Dilated cardiomyopathy, edema, alcoholism or malnutrition
Wet beriberi (thiamine [Vitamin B1] deficiency)
Dry eyes, dry mouth, arthritis
Sjogren syndrome (autoimmune destruction of exocrine glands)
Dysphagia (esophageal webs), glossitis, iron deficiency anemia
Plummer-Vinson syndrome (may progress to esophageal squamous cell carcinoma)
Elastic skin, hypermobility of joints
Ehlers-Danlos syndrome (Type III collagen defect)
Enlarged, hard left supraclavicular nodes
Virchow’s Node (abdominal metastasis)
Erythroderma, lymphadenopathy, hepatosplenomegaly, atypical T cells
Mycosis fungoides (cutaneous T-cell lymphoma) or Sezary Syndrome (mycosis fungoides + malignant T cells in blood)
Facial muscle spasm during tapping
Chvostek sign (hypocalcemia)
Fat, female, forty, and fertile
Cholelithiasis (gallstones)
Fever, chills, headache, myalgia following antibiotic treatment for Syphilis
Jarisch-Herxheimer reaction (rapid lysis of spirochetes results in toxin release)
Fever, cough, conjunctivitis, coryza, diffuse rash
Measles
Fever, night sweats, weight loss
B symptoms (staging) of lymphoma
Gout, intellectual disability, self-mutilating behavior in boy
Lesch-Nyhan Syndrome (HGPRT deficiency, X-linked recessive)
Fibrous plaques in soft tissue of penis
Peyronie disease (connective tissue disorder)
Green-yellow rings around peripheral cornea
Kayser-Fleischer rings (copper accumulation from Wilson disease); Low Ceruplasmin, low serum, high urinary copper. Treat w/ Penicilliamine
Hamartomatous GI polyps, hyperpigmentation of mouth/feet/hands
Peutz-Jeghers syndrome (inherited, benign polyposis can cause bowel obstruction; inc cancer risk, mainly GI)
Hepatosplenomegaly, osteoporosis, neurologic symptoms
Gaucher disease (glucocerebrosidase deficiency)
Hereditary nephritis, sensorineural hearing loss, cataracts
Alport syndrome (mutation in collagen IV)
Hyperphagia, hypersexuality, hyperorality, hyperdocility
Kluver-Bucy syndrome (bilateral amygdala lesion)
Hyperreflexia, hypertonia, Babinski sign present
UMN damage
Hyporeflexia, hypotonia, atrophy, fasciculations
LMN damage
Hypoxemia, polycythemia, hypercapnia
Blue Bloater (chronic bronchitis: hyperplasia of mucous cells)
Indurated, ulcerated genital lesion
Nonpainful: chancre (1˚ syphilis, Trepnenma palldium)Painful, with exudate: chancroid (Haemophilus ducreyi)
Infant with cleft lip/palate, micocephaly or holoprosencephaly, polydactyly, cutis aplasia
Patau syndrome (Trisomy 13)
Infant with failure to thrive, hepatosplenomegaly, and neurodegeneration
Niemann-Pick disease (genetic phingomyelinase deficiency)
Infant with hypoglycemia, failure to thrive, and hepatomegaly
Cori disease (debranching enzyme deficiency, alpha- 1,6 glucosidase) or Von Gierke disease (glucose-6-phosphatase deficiency, more severe, lactate)
Infant with microcephaly, rocker-bottom feet, clenched hands, and structural heart defect
Edwards syndrome (trisomy 18)
Jaundice, palpable distended non-tender gallbladder
Courvoisier sign (distal obstruction of biliary tree)
Large rash with bull’s-eye appearance
Erythemia chronicum migrans form Ixodes tick bite (Lyme disease: Borrelia)
Lucid interval after traumatic brain injury
Epidural hematoma (middle meningeal artery rupture)
Male child, recurrent infections, no mature B cells
Bruton disease (X-linked agammaglobulinemia due to bad bruton’s tyrosine kinase)
Mucosal bleeding and prolonged bleeding time
Glanzmann thrombasthenia (defect in platelet aggregation due to lack of GpIIb/IIIa)
Muffled heart sounds, distended neck veins, hypotension
Beck triad of cardiac tamponade (pressure on the heart that occurs when blood or fluid builds up in the space between the heart muscle [myocardium] and the outer covering sac of the heart [pericardium])
Myopathy (infantile hypertrophic cardiomyopathy), exercise intolerance
Pompe Disease (lysosomal alpha-1,4-glucosidase deficiency)
Neonate with arm paralysis following difficult birth
Erb-Duchenne palsy (superior trunk [C5-C6] brachial plexus injury: waiter’s tip)
No lactation postpartum, absent menstruation, cold intolerance
Sheehan syndrome (pituitary infarction)
Nystagmus, intention tremor, scanning speech, bilateral internuclear ophthalmoplegia
Multiple Sclerosis
Oscillating slow/fast breathing
Cheyne-Stokes respirations (central apnea in CHF or increased intracranial pressure)
Painful blue fingers/toes, hemolytic anemia
Cold agglutinin disease (autoimmune hemolytic anemia caused by Mycoplasma penumoniae, infectious mononucleosis)
Painful, pale, cold fingers/toes
Raynaud phenomenon (vasospasm in extremities)
Painful, raised red lesions on pad of fingers/toes
Osler nodes (infective endocarditis, immune complex deposition)
Painless erythematous lesions on palms and soles
Janeway lesions (infective endocarditis, septic emboli/microabscesses)
Painless jaundice
Cancer of the pancreatic head obstructing bile duct
Palpable purpura on buttocks/legs, joint pain (child), hematuria
Henoch-Schonlein purpura (IgA vasculitis affecting skin and kidneys)
Pancreatic, pituitary, parathyroid tumors
MEN I (autosomal dominant)
Pink complexion, dyspnea, hyperventilation
Pink Puffer: emphysema: centriacinar [smoking], panacinar [alpha1-antitrypsin deficiency], PAS + staining)
Polyuria, renal tubular acidosis Type II, growth failure, electrolyte imbalances, hypophosphatemic rickets
Fanconi syndrome (proximal tubular reabsorption defect)
Pruritic, purple, polygonal planar papules and plaques
Lichen planus
Ptosis, miosis, anhidrosis
Horner Syndrome (sympathetic chain lesion)
Pupil accommodates but doesn’t react
Argyll Robertson pupil (neurosyphilis)
Rapidly progressive leg weakness that ascends following GI/upper respiratory infection
Guillian-Barre syndrome (acute autoimmune inflammatory demyelinating polyneuropathy); camplobacter jejuni
Rash on palms and soles
Coxsackie A, 2˚ syphilis, Rocky Mountain Spotted fever
Recurrent colds, unusual eczema, high serum IgE
Hyper-IgE syndrome (Job syndrome: neutrophil chemotaxis abnormality)
Red current jelly sputum in alcoholic or diabetic patient
Klebsiella penumoniae
Red current jelly stools
Acute mesenteric ischemia (adults), intussusception (infants)
Red, itchy, swollen rash of nipple/aerolea
Paget disease of the breast (sign of underlying neoplasm)
Red urine in the morning, fragile RBCs
Paroxysmal nocturnal hemoglobinuria (no PIG therefore cannot attach DAF (CD55) and MIRL (CD59)
Renal cell carcinoma (bilateral), hemagioblastomas, angiomatosis, pheechromocytoma
von Hippel-Lindau disease (dominant tumor suppressor gene mutation)
Resting tremor, rigidity, akinesia, postural instability
Parkinson disease (nigrostriatal dopamine depletion)
Retinal hemorrhages with pale centers
Roth spots (bacterial endocarditis)
Severe jaundice in neonate
Crigler-Najjar syndrome (congenital unconjugated hyperbilirubinemia)