USMLE Step 1 for International clients, Quizzes of Medicine

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2025/2026

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USMLE Step 1
Heterophile ab NEGATIVE Mono-like syndromes
*CMV
HHV-6
HIV
Toxoplasmosis
Wernicke's Aphasia
-word salad: well-articulated, nonsensical speech paired with lack of lang comprehension
-aud association cortex: post part of sup temporal gyrus
- supplied by MCA
Congenital Deficiency of Propionyl CoA Carboxylase
-prevents conversion of propionyl CoA to methylmalonyl CoA
-propionyl CoA derived from= val, ile, met, thr, odd # FA, cholesterol side chains
-Propionic Acidemia: poor feeding, vomiting, hypotonia, lethargy, dehydration, anion gap
acidosis
Down Synd Comorbidities
Neuro: MR, early onset Alzheimer's
Cardio: complete AV septal defect, VSD, ASD
GI: duodenal atresia, hirschprung disease
Endo: hypothyroid, DM1, obesity
Heme: ALL (> 5 yo) and AML (<5 yo)
Rheumatology: atlantoaxial stability
MCC of Hypoglycemia in EtOH-ics
Thiamine def= suppression of GNG (pyruvate DH) and TCA cyle (alpha-KG DH)
MCC of Hypoglycemia in advanced renal insuff
impaired clearance of insulin
Avoid Nitrates in Hypertrophic Cardiomyopathy bc...
Nitrates decrease preload, which will increase the LV outflow tract... BUT since the ventricle
is abnormally shaped, there is an outflow obstruction
Mets through BM
Clonal proliferation of cells can invade/ metastasize*
1. malignant cells to lose their cell-to-cell adhesion molecules (cadherins)
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USMLE Step 1

Heterophile ab NEGATIVE Mono-like syndromes *CMV HHV- 6 HIV Toxoplasmosis Wernicke's Aphasia

  • word salad: well-articulated, nonsensical speech paired with lack of lang comprehension
  • aud association cortex: post part of sup temporal gyrus
  • supplied by MCA Congenital Deficiency of Propionyl CoA Carboxylase
  • prevents conversion of propionyl CoA to methylmalonyl CoA
  • propionyl CoA derived from= val, ile, met, thr, odd # FA, cholesterol side chains
  • Propionic Acidemia: poor feeding, vomiting, hypotonia, lethargy, dehydration, anion gap acidosis Down Synd Comorbidities Neuro: MR, early onset Alzheimer's Cardio: complete AV septal defect, VSD, ASD GI: duodenal atresia, hirschprung disease Endo: hypothyroid, DM1, obesity Heme: ALL (> 5 yo) and AML (<5 yo) Rheumatology: atlantoaxial stability MCC of Hypoglycemia in EtOH-ics Thiamine def= suppression of GNG (pyruvate DH) and TCA cyle (alpha-KG DH) MCC of Hypoglycemia in advanced renal insuff impaired clearance of insulin Avoid Nitrates in Hypertrophic Cardiomyopathy bc... Nitrates decrease preload, which will increase the LV outflow tract... BUT since the ventricle is abnormally shaped, there is an outflow obstruction Mets through BM Clonal proliferation of cells can invade/ metastasize*
  1. malignant cells to lose their cell-to-cell adhesion molecules (cadherins)
  1. cell receptors to attach to laminin (a glycoprotein) in the basement membrane and to release metalloproteinases (e.g., collagenases, stromelysins, gelatinases) to degrade the basement membrane and other enzymes to degrade the interstitial connective tissue- tissue inhibitors of metalloproteinases neutralize these tumor-produced enzymes and limit the degree of invasion
  2. cell receptors to attach to bronectin and other proteins in the extracellular matrix (ECM) and to break it down
  3. malignant cells to produce cytokines that stimulate locomotion, so that they can move through basement membranes and the intracellular and extracellular matrices Bicuspid Aortic Valve Commonly presents in young, asymptomatic patient with soft systolic ejection at right 2nd ICS
  • can cause aortic regurg MCC of Vaginal Candidiasis
  1. Abx use= reduces lactobacilli pop
  2. High estrogen levels- preg
  3. System corticosteroid therapy
  4. Uncontrolled DM
  5. Immunosuppression, including HIV Drug causes of SIADH
  • Carbamazepine
  • Cyclophosphamide
  • SSRI MC Ankle Sprain due to inversion of plantar-flexed foot
  • Ant Talofibular Lig dmg
  • ecchymosis at the ant-lat aspect of the ankle Upper Brachial Plexus Injury
  • Musculocutaneous and Suprascapular N.
  • dystocia mc in neonates; severe trauma mc in adults
  • should adduction, elbow extension, and forearm pronation Patent foramen ovale
  • failure of septum primum and septum secundum to fuse after birth
  • can lead to paradoxical emboli Ventricular Septal Defect

S. epidermidis

  • coag neg
  • novobiocin sens
  • infective endocarditis and infective arthritis in prosthetic pts Asymptomatic heart defect in turner's synd
  • nonstenotic bicuspid aortic valve
  • early systolic , high frequency click over right second IC space Cardiac Changes w/ Normal Aging
  • decreased left ventricular chamber size
  • shortened base- to- apex dimension
  • ventricular septum becomes sigmoid and shape, with basilar portion bulging into LV outflow tract
  • atrophy of myocardium causes increased interstitial connective tissue, often with concomitant extracellular amyloid deposition
  • lipofucin pigment accumulation within cardiomyocytes ARDS Characterized by the development of hypoxemia and bilateral pulmonary infiltrates in the absence of heart failure
  • begins with initial injury of pul alveoli (smoke inhal) or pul endothelium (sepsis) which leads to the recruitment of neutrophils- this worsens the situation and leads to intraalveolar accumulation and hyaline membrane formation
  • decreased lung compliance, increased work of breathing, worsened V/Q mismatch, and normal PCWP Renal Artery Stenosis (histo) medial fibroplasia, absent internal elastic lamina in areas of aneurysmal dilation Paget's Disease associate Bone Tm OSTEOSARCOMA! arising from tibia, femur, humerus, and other bones
  • pain doesnt resolve with OTC analgesics DNA Laddering (Gel Electrophoresis)
  • DNA fragments in multiples of 180 bp each
  • sensitive indicator of APOPTOSIS
  • laddering done by specific endonucleases during haryorrhexis, cleaving DNA at interucleosomal linker regions
  • this is not seen in cancer cells, since they evade apoptosis

Warburg Effect malignant cells undergo high rates of glycolysis to produce macromolecules necessary to sustain rapid cellular growth Risk Factors of Endometritis

  • C-section delivery
  • chorioamnionitis
  • group B strep colonization
  • intrauterine instrumentation
  • preterm delivery
  • prolonged labor
  • prolonged ruptured membranes
  • retained products of conception SIGNS AND SX OF POSTPARTUM ENDOMETRITIS
  • fever
  • leukocytosis
  • uterine tenderness
  • foul smelling vaginal discharge Metabolic derangements assoc with DKA metabolic acidosis, ketonemia, hyperglycemia, hyperkalemia, hyponatremia
  • hyperammonemia can be observed due to muscle degradation Pulmonary Embolism V/Q Mismatch, causes hypoxemia that increases ventilation and HR via a chemoreceptor reflex
  • hypocapnia b/c hypervent, but unable to compensate for hypoxemia
  • resp alkylosis= increased ph and decreased PaCO Acanthosis Nigracans
  • Obesity/ insulin resistance
  • Malignancy of GI or Lungs Congenital Pyloric Stenosis
  • thickening of stomach wall, hypertrophy of smooth muscle pyloric stenosis
  • palpable olive mass- epigastric region
  • nonbilious projectile vomiting at 2-6 weeks of age
  • assoc w/ Macrolides
  • hypokalemia, hypochloremic, metab alkalosis
  • inhib Ca2+ conductance
  • inhib transmitter release neonatal intravascular hemorrhage
  • mc in fragile germinal matrix
  • inc freq with decreased age and birth wt
  • mc complication would be long term neurodev impairment (alt consciousness, hypotonia, dec spont mvmnt)
  • s/sx of bleed: bulging ant frontanelle, hypotension, decerebrate posturing, tonic-clonic seizures, irreg respirations, coma Acute Rheumatic fever
  • endemic in dev countries
  • molecular mimicry: anti group a strep ab attack host antigens on cardiac and neuronal tissue approx 2-4 weeks post acute pharyngitis (aka cross reactivity of ab against bacterial and host antigens)
  • acute/subacute: migratory arthritis, pancarditis, Sydenham chorea
  • Chr: mitral regurg/ stenosis
  • tx: PCN Spironolactone + HF improve survival of CHF pts with low LV ejection fraction
  • block aldosterone's effect on heart and decrease fibrosis and ventricular remodeling
  • used with ace-inhib and beta-blockers Common S/E of Thiazide Diuretics acute kidney injury, decreased Na+ and K+, hyperuricemia/ acute gout, elevated glu and cholesterol levels Common S/E of ACE-Inhib cough, angioedema, inc K+ CCB (diphenhydropine) S/E periph edema, dizziness/ lightheadedness Beta Blocker S/E bronchospasm, bradycardia, fatigue, sexual dysfunction HTN and at risk for Osteoporosis THIAZIDES! increased bone mineral density b/c increase in Ca2+ abs in DCT Methylmalonyl-CoA mutase Def

- AR

  • increased urine: methylmalonic acid and propionic acid
  • hyperammonemia, ketotic hypoglycemia, and metab acidosis
  • newborns present with lethargy, vomiting, and tachypnea TCA Effect on Cardiac Na+ Channel BLOCKS cardiac fast Na+ channels= QT and QRS prolongation and arrhythmias
  • treated with Sodium Bicarb MC Complication post Subarachnoid Hemorrhage SAH sx: thunderclap ha, confusion, fever, nuchal rigidity MC Compl: VASOSPASM!
  • vessels surrounding ruptured aneurysm
  • cerebral ischemia and new onset confusion and/or focal neuro deficits (paresthesia, weakness, etc) 4-12 days post SAH
  • mech of vasospasm is related to impaired brain autoreg
  • not seen on CT, need transcranial color doppler
  • Nimodipine prescribed to prevent vasospasm post-SAH Most Serious Compl of SAH REBLEED!
  • sudden dev of severe confusion, HA, N/V, decreased consciousness, focal neuro deficits
  • seen on CT t(8;14) Burkitt lymphoma (c-myc activation)
  • cmyc is an oncogene
  • very aggressive, rapid proliferation of cell growth t(9;22) aka Philadelphia chromosome CML (BCR-ABL hybrid), rarely ALL
  • constitutive expression of tyrosine kinase
  • poor prognosis when expressed in ALL t(11;14) Mantle cell lymphoma (cyclin D1 activation)
  • cyclin D1 is a cell cycle regulator
  • this translocation continuously allows cells to go on in cell cycle without stopping/ apoptosis t(14;18)
  • M spike on serum protein electrophoresis
  • Ig light chains in urine (Bence Jones protein)
  • Activated IgG prod by plasma cells by IL-6, may lead to proteasome inhib
  • Rouleaux formation (RBCs stacked like poker chips in blood smear) CO Poisoning Normal PO2 (dissolved O2) Decreased %sat of Hb Decreased total O2 content = makes Fe2+ into Fe3+(ferric), leading to the formation of methemoglobin which cannot bind to O2- this causes a left shift on the saturation curve- methemoglobin will present with cyanosis causes dusky discoloration in skin Pure Red Cell Aplasia (PRCA)
  • Inhib of erythroid precursors and progenitors by IgG autoantibodies or cytotoxic T cells
  • Marrow failure characterized by hypoplasia of erythroid elements but normal granulopoiesis and thrombopoiesis
  • Assoc with thyoma, lymphocytic leukemias, and parvovirus B19 infection Asthma Dec FEV1/ FVC Exp wheeze Caused by env and genetics Chr Eosinophil Bronch: IL-5 by TH2 cells MPB= bronch epith dmg- mc in exercise induced asthma Cause of LVHF shortness of breath Impaired diastolic return of Pul v. because high end diastolic pressure causes an increase in hydrostatic pressure and transudate leaks out into the interstitium--> causes affected tissue to swell and increased resistance of movement due to decreased lung compliance = the neg pressure generated normally from inspiration isnt enough to distend the lungs, causing poor gas exchange and sob Reduced pulmonary compliance
  • LV Heart Failure + Pul Congestion
  • Pul Fibrosis
  • Insuff Surfactant

decreased compliance= decreased FRC Surfactant

  • cortisol/ thyroxine ↑synthesis
  • insulin ↓ synthesis Pulmonary infarction
  • Pulmonary infarction: MC site lower lobes
  • Saddle embolus: sudden death
  • dyspnea/tachypnea MC symptom/sign
  • respiratory alkalosis; hypoxemia; ↑D-dimers Caplan syndrome pneumoconiosis + cavitating rheumatoid nodules Perfusion-limited gas exchange
  • diffusion can increase only if blood flow increases
  • examples: N2O and O2 under normal conditions Diffusion-limited gas exchange
  • diffusion continues as long as pressure gradient exists across pulmonary membrane
  • examples: O2 during vigorous exercise at high altitude and CO pathophysiologic mechanisms that reduce diffusing capacity (1) increased thickness of the pulmonary membrane in restrictive diseases (the primary factor in silicosis and idiopathic pulmonary fibrosis) (2) collapse of alveoli and lung segments (atelectasis), which contributes to a decreased surface area available for gas exchange (e.g., with bed rest after surgery) (3) poor lung compliance, resulting in insufficient ventilation (e.g., silicosis) (4) destruction of alveolar units, which also decreases surface area (e.g., emphysema) Physiologic shunt
  • This occurs when blood is appropriately directed to the lungs but is not involved in gas exchange
  • EX bronchial arterial circulation= The bronchial arteries supply the bronchi and supporting lung parenchyma but are not involved in gas exchange at the level of the alveoli Physiological Shunts in Pathological Cases (Disease states)
  • FEV1 is reduced more than is FVC, and the FEV1/FVC ratio is reduced
  • increased TLC Mechanically Ventilated Patients
  • The amount of anatomic dead space increases considerably b/c the volume of space occupied by the respiratory apparatus from the patient's mouth to the ventilator must be considered to be anatomic dead space
  • Alveolar ventilation is altered, and care must be taken to ensure adequate oxygenation Decreased Alv Ventilation
  • falls to a level too low to provide sufficient oxygen to the tissue, patients must compensate by increasing the rate of breathing (tachypnea) or by taking larger-volume tidal breaths
  • taking larger tidal breaths would be better because it minimizes the effect of dead space on alveolar ventilation Elevated Alveolar-Arterial Gradient: V/Q Mismatch
  • Pulmonary embolism
  • Airway obstruction
  • Interstitial lung disease Elevated Alveolar-Arterial Gradient: Shunt
  • Intracardiac Shunt (VSD)
  • Intrapulmonary Shunt (pulmonary AVM, pneumonia, CHF)
  • Atelectasis Elevated Alveolar-Arterial Gradient: Diffusion defects
  • Pulmonary fibrosis
  • Emphysema
  • Asbestosis Ureteric Bud
  • caudal end of mesonephric duct
  • gives rise of ureter, pelvises, calyces, and collecting ducts
  • canalized by 10th week Metanephric Mesenchyme
  • interacts with ureteric bud that induces differentiation and formation of glomerulus through the distal convoluted tubules Renal Artery Stenosis
  • MCC: atherosclerosis or fibromuscular hyperplasia. In unilateral renal artery stenosis, hypertension may occur because decreased perfusion of the affected kidney is incorrectly "interpreted" as intravascular volume depletion, which triggers a neurohormonal cascade response (the RAAS and ADH)--> causing fluid retention and vasoconstriction resulting in hypertension
  • When both renal arteries are affected (bilateral renal artery stenosis), renal blood flow may become so compromised that the kidneys are unable to perform their normal recycling functions, resulting in the toxic accumulation of metabolic byproducts Loop Diuretic effect on Tubuloglomerular Feedback
  • The juxtaglomerular apparatus is informed of NaCl in the tubular lumen by virtue of its transport into the cells of the macula densa by the same Na+-K+-2Cl- cotransporter that is inhibited by loop diuretics
  • One reason for the potency of loop diuretics is their ability to blunt tubuloglomerular feedback and thereby maintain GFR (and urine production) despite increased NaCl traffic past the macula densa Acute Tubular Necrosis
  • MCC: acute renal failure-- which results when hypotension (ischemia, hypoxemia) or tubular toxins damage renal tubular epithelial cells
  • Dysfunction of these cells--> sodium and water reabsorption in the proximal tubule is impaired
  • Large amounts of NaCl and water are therefore presented to the macula densa-- via tubuloglomerular feedback, this decreases renal blood flow and GFR by stimulating vasoconstriction of the afferent arteriole
  • The subsequent decrease in GFR may play a role in limiting potentially life- threatening losses of sodium and water that might otherwise occur in ATN PCT: Isosmotic reabsorption reabsorption of fluid along the proximal tubule in which there is no change in tubular osmolality Glomerulotubular balance balance among GFR, peritubular oncotic pressure, and proximal tubular reabsorption Response to volume- depleted state Decreased RPF --> Increased filtration fraction to maintain GFR --> Increased peritubular oncotic pressure --> Increased proximal tubular reabsorption --> Increased ECF volume Response to volume- expanded state
  • These occur because the resting membrane potentials of nerves and muscle are directly related to the ratio of intracellular and extracellular potassium concentrations Drugs that cause hyperkalemia = inability of potassium to be moved intracellularly
  • digitalis
  • insulin
  • abuterol Patient with HTN and Hypokalemia = increased renin and increased aldosterone SECONDARY HYPERALDOSTERONISM
  • renovasc htn ( renal a. stenosis)
  • malignant HTN
  • renin secreting tm (JG cell tm)
  • diuretic use Patient with HTN and Hypokalemia = decreased renin and increased aldosterone PRIMARY HYPERALDOSTERONISM
  • Aldosterone prod Tm
  • Bilateral adrenal hyperplasia Patient with HTN and Hypokalemia = decreased renin and decreased aldosterone
  • CAH
  • Adrenal tumor
  • Cushing Synd
  • Exogenous mineralocorticoid MM Symptoms
  • fatigue= d/t anemia
  • constipation= d/t hypercalcemia
  • bone pain, mostly in the back and ribs= d/t osteoclast activating factor prod by myeloma cells
  • elevated serum protein= monoclonal protein
  • renal failure
  • "myeloma kidney"= excess excretion of free light chains (bj proteins), and when the levels exceed the reabs capacity they will precipitate with Tamm Horsfall protein and form casts that cause tubular obstruction and epithelial injury --> tubular dysfxn
  • glassy casts stain eosinophillic Leukocyte adhesion defciency (LAD)
  • due to selectin or CD11a/ CD18 deficiency aka and integrin defect
  • Delayed separation of the umbilical cord (usually separates and sloughs by the end of the second postnatal week)-- Neutrophil enzymes are important in cord separation; therefore in a histologic section of the surgically removed umbilical cord, no neutrophils would be seen adhering to venular endothelium or be seen in the interstitial tissue
  • Additional clinical findings include severe gingivitis, poor wound healing, and peripheral blood neutrophilic leukocytosis (loss of the marginating pool)
  • Recurrent bact infections without pus Lupus related thrombosis
  • DVT
  • hepatic v. thrombosis
  • placental thrombosis (recurrent preg loss)
  • stroke TX: lifelong anticoag Bone Marrow Stem Cells CD Opioids cause biliary colic
  • act on mu rec to constrict sphincter of oddi= increased pressure of common bile duct and gallbladder
  • need to discontinue drug and treat pain with other NSAIDS: ketorolac and diclofenac P-Glycoprotein
  • Also known as multidrug resistance protein 1 (MDR1)--transmembrane ATP-dep efflux pump protein with broad specificity for hydrophobic compounds
  • Classically seen in adrenal cell carcinoma but also expressed by other cancer cells (eg, colon, liver)
  • Used to pump out toxins, including chemotherapeutic agents (one mechanism of responsiveness or resistance to chemotherapy over time) Hereditary Orotic Aciduria defect in UMP Synthase physical and mental retardation megaloblastic anemia elev urinary orotic acid benefit from uridine supplement Spontaneous Intracranial Hemorrhage
  • Decreased CO
  • LVH and dilation
  • Austin Flint murmur= blood hits the anterior leaflet of of aortic valve
  • Aortic valve is incompetent= high-pitched diastolic blowing murmur --early diastole; decreases in intensity throughout diastole (decrescendo)
  • Turbulent flow back into left ventricle from the high-pressure aorta
  • Can cause Pul HTN
  • Causes: Syphillis (3) induced aortic aneurysm, CT disorders, endocarditis
  • sx: fatigue, syncope, SOB, palpitations Mitral Stenosis
  • Associated with large diastolic pressure difference between left atrium and ventricle
  • Increased left atrial pressures --> increased hydrostatic pressures in pulmonary circulation -
  • > pulmonary edema --> RVH and decreased CO
  • Sx of pulmonary edema: dyspnea, reduced exercise capacity
  • Opening snap + diastolic rumble (diastolic murmur)
  • Turbulent flow across stenotic mitral valve during ventricular filling
  • LA pushes on esoph
  • LA hypertrophy and dilation Mitral Regurg
  • mitral valve does not form good seal--> blood flows into left atrium during early systole
  • Precise symptoms of mitral regurgitation depend on temporal course of the mitral regurgitation
  • acute onset--> severe symptoms
  • chronic onset--> typically asymptomatic or minor symptoms
  • MVP: classically gives rise to a midsystolic "click" on auscultation
  • Turbulent flow into left atrium during ventricular systole
  • Murmur lasts throughout systole Systolic heart failure pump failure (impaired contractility, increased afterload) Diastolic heart failure impaired ventricular filling during diastole due to stiff ventricle or obstruction to ventricular filling (e.g., mitral stenosis) Estrogen-containing oral contraceptives
  • Inhibiting the LH surge that is responsible for ovulation
  • Estrogen-containing contraceptives provide a constant level of estrogen that maintains a

continual negative feedback on pituitary gonadotropin secretion, thereby stabilizing FSH and LH secretion Progesterone-only OCPs

  • 50% effective in inhibiting ovulation
  • work primarily by thickening the cervical mucus and altering the motility and secretions of the fallopian tubes, as well as thinning the endometrium
  • All these changes make the uterus a less hospitable environment for implantation of a fertilized embryo
  • Inhibits implantation and therefore pregnancy, it does not prevent fertilization Precocious puberty
  • Normal karyotype
  • Premature maturation of arcuate nucleus in hypothalamus
  • Treat with GnRH agonists (e.g., leuprolide) 5a-Reductase deficiency
  • Normal karyotype
  • Insufficient conversion of testosterone to active dihydrotestosterone form
  • Female develops internal male genitalia
  • Ambiguous external then male external during puberty Klinefelter syndrome
  • 47,XXY karyotype
  • Meiotic nondisjunction of X chroms
  • Male with eunuchoid body, gynecomastia, testicular atrophy, tall, long extremities, female hair distribution, dev delay, infertility, some psychosocial abnorm (lack of insight or judgment)
  • Testicular atrophy; fibrosis seminiferous tubules/Sertoli cells; Leydig cells prominent
  • Dysgenesis of seminiferous tubules --> decreased inhibin---> increased FSH
  • Abnormal Leydig cell function--> decreased testosterone --> increased LH--> increased estrogen Androgen insensitivity syndrome (male pseudohermaphroditism)
  • XY karyotype
  • Androgen receptor defect
  • Male internal genitalia but incompletely virilized, ambiguous, or female external genitalia
  • These individuals do not have male internal genitalia (no epididymis, seminal vesicles, vas deferens, prostate), and most have normal female-looking external genitalia with a blind- ending vaginal pouch