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FIRST AID FOR THE USMLE COMPREHENSIVE TEST BANK COMPLETE QUESTIONS AND VERIFIED SOLUTIONS

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FIRST AID FOR THE USMLE COMPREHENSIVE TEST BANK COMPLETE QUESTIONS AND VERIFIED SOLUTIONS

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FIRST AID FOR THE USMLE
COMPREHENSIVE TEST BANK COMPLETE
QUESTIONS AND VERIFIED SOLUTIONS

●● Abdominal pain, diarrhea, leukocytosis, recent antibiotic use
Answer: Clostridium difficile infection


●● Achilles tendon xanthoma
Answer: Familial hypercholesterolemia (decreased LDL receptor
signaling)


●● Adrenal hemorrhage, hypotension, DIC
Answer: Waterhouse-Friderichsen syndrome (menengococcemia)


●● Anaphylaxis following blood transfusion
Answer: IgA deficiency


●● Anterior "drawer sign" ⊕
Answer: Anterior cruciate ligament injury


●● Arachnodactyly, lens dislocation, aortic dissection, hyperflexible
joints

,Answer: Marfan syndrome (fibrillin defect)


●● Athlete with polycythemia
Answer: 2° to erythropoietin injection


●● Back pain, fever, night sweats
Answer: Pott disease (vertebral TB)


●● Bilateral acoustic schwannomas
Answer: Neurofibromatosis type 2


●● Bilateral hilar adenopathy, uveitis
Answer: Sarcoidosis (noncaseating granulomas)


●● Black eschar on face of patient with diabetic ketoacidosis
Answer: Mucor or Rhizopus fungal infection


●● Blue sclera, brittle bones
Answer: Osteogenesis imperfecta (type I collagen defect)


●● Bluish line on gingiva
Answer: Burton line (lead poisoning)

,●● Bone pain, bone enlargement, arthritis
Answer: Paget disease of bone (osteoblastic and osteoclastic activity)


●● Bounding pulses, diastolic heart murmur, head bobbing
Answer: Aortic regurgitation


●● "Butterfly" facial rash and Raynaud phenomenon in a young female
Answer: Systemic lupus erythematosus


●● Café-au-lait spots, Lisch nodules (iris hamartoma), cutaneous
neurofibromas, pheochromocytomas, optic gliomas A
nswer: Neurofibromatosis type I, pheochromocytoma, optic gliomas


●● Café-au-lait spots (unilateral), polyostotic fibrous dysplasia,
precocious puberty, multiple endocrine abnormalities A
nswer: McCune-Albright syndrome (mosaic G-protein signaling
mutation)


●● Calf pseudohypertrophy
Answer: Muscular dystrophy (most commonly Duchenne, due to X-
linked recessive frameshift mutation of dystrophin gene)

, ●● Child with cervical lymphadenopathy, desquamating rash, coronary
aneurysms, red conjunctivae and tongue
Answer: Kawasaki disease (treat with IVIG and aspirin)


●● "Cherry-red spots" on macula
Answer: Tay-Sachs (ganglioside accumulation) or Niemann-Pick
(sphingomyelin accumulation), central retinal artery occlusion


●● Chest pain on exertion
Answer: Angina (stable: with moderate exertion; unstable: with minimal
exertion or at rest)


●● Chest pain, pericardial effusion/friction rub, persistent fever
following MI
Answer: Dressler syndrome (autoimmune-mediated post-MI fibrinous
pericarditis, 2-12 weeks after acute episode


●● Chest pain with ST depressions on EKG
Answer: Unstable angina (troponins −) or NSTEMI (troponins +)


●● Child uses arms to stand up from squat
Answer: Gowers sign (Duchenne muscular dystrophy)

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