Respiratory Flashcards

(100 cards)

1
Q

Lung mass of a nonsmoker genes

A

EGFR and ALK

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2
Q

Lung mass of a nonsmoker

A

Adenocarcinoma

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3
Q

Mass in the lung with a keratin pearl

A

squamous cell carcinoma

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4
Q

This is found in the lung- what type of cancer

A

Small cell lung cancer arises in a blue cells with scant cytoplasma nd indistinct nucleui

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5
Q

Which lung cancers are central

A

Suqamous cell carcinoma and small cell carcinoma

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6
Q

What are klutichsky cells

A

Dark purple neuroendocrine cells found in small cell carcinoma

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7
Q

Small cell lung cancer oncogene

A

L-myc

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8
Q

What are the markers of small cell lung cancer

A

Chromagranin, Synaptophysin, NCAM, CD56,

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9
Q

Small cell lung cancer is associated with what conditions

A

SIADH, Lambert Eaton, Cushing Syndrome

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10
Q

What is a superior sulcus tumor

A

A pancoast tumor

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11
Q

Clubbing of the fingers is most likely associated with

A

Lung cancer

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12
Q

Nail pitting is associated with

A

psoriasis

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13
Q

Koilonychia is associated with

A

theyre spoon nails and iron deficience

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14
Q

Half and Half nails aka Lindsay nails

A

Chronic renal failure

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15
Q

In PE what hppeens to PaO2 and PaCO2 and PH

A

lower PaO2 and PCo2 and higher pH due to hyperventilatio nand normal HCO3

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16
Q

A perfusion defect without ventilation defect

A

PE

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17
Q

Does PCO2 increase or decrease Ph!

A

More PCO2 = decrease Ph

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18
Q

Type I pneumocytes

A

Squamous. 97% of alveolar surfaces. Thinly line
the alveoli (two black arrows in A) for optimal
gas exchange.

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19
Q

Type II pneumocytes

A

Cuboidal and clustered A.
2 functions:
1. Serve as stem cell precursors for 2 cell
types (type I and type II cells); proliferate
during lung damage.
2. Secrete surfactant from lamellar bodies
(arrowheads in B).
Surfactant— alveolar surface tension,
alveolar collapse, lung recoil, and
compliance.
Composed of multiple lecithins, mainly
dipalmitoylphosphatidylcholine (DPPC).
Synthesis begins ~20 weeks’ gestation and
achieves mature levels ~35 weeks of gestation.
Corticosteroids important for fetal surfactant
synthesis and lung development.
2 (surface tension) Collapsing pressure (P) = radius
Law of Laplace—Alveoli have tendency to
collapse on expiration as radius .
Alveolar macrophages Phagocytose foreign materials; release cytokines
and alveolar proteases. Hemosiderin-laden
macrophages (heart failure cells) may be found
in the setting of pulmonary edema or alveolar
hemorrhage.

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20
Q

What are the key physiological changes and adaptations to high altitude?

A
  • At high altitude:

↓ Atmospheric O₂ (↓ PiO₂ → ↓ PaO₂)

↑ Ventilation → ↓ PaCO₂ → Respiratory alkalosis

Acute symptoms: headache, nausea, fatigue, lightheadedness, sleep disturbance

Chronic adaptations:

Sustained ↑ ventilation

↑ Erythropoietin → ↑ Hct & Hb (response to chronic hypoxia)

↑ 2,3-BPG → rightward shift of O₂ dissociation curve → ↑ O₂ release to tissues

Cellular changes: ↑ mitochondria density

Renal compensation: ↑ excretion of HCO₃⁻ (can be augmented with acetazolamide)

Chronic hypoxic pulmonary vasoconstriction → ↑ pulmonary vascular resistance → pulmonary hypertension → right ventricular hypertrophy (RVH)

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21
Q

A 28-year-old previously healthy man comes to the urgent care clinic due to shortness of breath. The patient is on a ski vacation in Breckenridge, Colorado, which is situated at an altitude of 2926 m (9600 ft). On arrival 4 days ago, he experienced mild headache and nausea that resolved spontaneously, but since yesterday, he has had worsening dyspnea and cough. The patient now feels short of breath even with minimal exertion. Temperature is 37.3 C (99.1) F, blood pressure is 134/82 mm Hg, pulse is 98/min, and respirations are 22/min. Oxygen saturation is 86% on ambient air, which rapidly improves to 95% with supplemental oxygen. Physical examination shows pink mucous membranes, flat neck veins, bilateral inspiratory crackles, and no heart murmurs or pedal edema. Chest x-ray reveals patchy alveolar infiltrates. Which of the following is the most likely cause of this patient’s current condition?
A. Alveolar-capillary membrane disruption
B. Embolic pulmonary arterial occlusion
C. Excessive decrease in PaCO2 level
D. Impaired left ventricular function
E. Increased total red blood cell mass

A

A. Alveolar-capillary membrane disruption

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22
Q

AAT deficiency causes early-onset panacinar emphysema, which predominantly affects

A

lower lung lobes.

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23
Q

Interchain cross-links involving _____ give elastin its elastic recoil property.

A

lysine (formed by lysyl oxidase)

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24
Q

What are the classic pulmonary examination findings in pleural effusion regarding breath sounds, tactile fremitus, and percussion?

A

Breath sounds: Decreased or absent

Tactile fremitus: Decreased

Percussion: Dullness

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25
According to Light’s criteria, a pleural effusion is exudative if any of the following are true:
Pleural fluid protein / serum protein > 0.5 Pleural fluid LDH / serum LDH > 0.6 Pleural fluid LDH > 2/3 the upper limit of normal serum LDH If none are met → transudative effusion.
26
Sabouraud agar has a pH of ~5.6 and high glucose content. What type of organisms does this favor?
Fungi (yeasts and molds), because acidic pH inhibits bacterial growth.
26
What are typical lab findings in transudative vs exudative pleural effusions?
Feature Transudate Exudate Protein Low (< 3 g/dL, PF/S < 0.5) High (> 3 g/dL, PF/S > 0.5) LDH Low (< 200 U/L, PF/S < 0.6) High (> 200 U/L, PF/S > 0.6) Appearance Clear, straw-colored Cloudy, sometimes bloody or purulent WBCs < 1000, mostly mononuclear Usually higher, often neutrophils if infection
27
Which class of antifungals works by blocking ergosterol synthesis in fungal cell membranes?
Azoles (e.g., fluconazole, itraconazole).
28
A patient with tinea corporis is cultured on Sabouraud agar. Which oral antifungal works by inhibiting ergosterol synthesis?
Terbinafine (inhibits squalene epoxidase) or azoles (inhibit lanosterol demethylase).
29
A 22-year-old woman with a history of anorexia nervosa and intense exercise presents with secondary amenorrhea. She is admitted for nutritional rehabilitation. Within the first 48 hours of refeeding, which electrolyte is most likely to decrease first? A) Sodium B) Potassium C) Phosphate D) Calcium E) Magnesium
Phosphate ✅ Explanation: This patient is at risk for refeeding syndrome. During starvation, insulin levels are low, and intracellular phosphate is depleted. Refeeding (especially carbohydrates) causes a sudden rise in insulin → drives phosphate into cells for ATP production. Result: Rapid hypophosphatemia. Other electrolyte changes: Potassium and magnesium may also fall, but phosphate is the first to decrease. High-yield USMLE tip: Watch for muscle weakness, respiratory failure, arrhythmias, or hemolysis in malnourished patients during initial nutrition.
30
31
Brown discoloration around the ankles with edema and ulceration
venous stasis dermatitis.
32
A 7-year-old presents with sore throat, fever, tonsillar exudates, and a sandpaper-like rash. Gram stain: β-hemolytic cocci in chains. Most likely organism?
Streptococcus pyogenes (GAS) High-Yield Associations: Pharyngitis / Tonsillitis Scarlet fever (erythrogenic toxin) Impetigo, cellulitis, erysipelas Necrotizing fasciitis Post-strep complications: rheumatic fever (pharyngitis only), post-strep glomerulonephritis Lab Clues: Bacitracin sensitive PYR positive
33
A newborn develops sepsis and meningitis on day 2 of life. Blood culture: β-hemolytic, Gram-positive cocci in chains. Most likely organism?
Streptococcus agalactiae (GBS) High-Yield Associations: Neonatal sepsis & meningitis UTIs in adult women Lab Clues: Bacitracin resistant CAMP test positive
34
Chronic alcoholic presents with confusion, ataxia, and horizontal nystagmus. Most likely diagnosis?
Acute Wernicke Encephalopathy Cause: Thiamine (B1) deficiency Eye finding: horizontal gaze palsy / nystagmus Treatment: IV thiamine (before glucose)
35
Which feature distinguishes acute Wernicke from chronic Korsakoff?
Acute Wernicke: confusion, ataxia, ophthalmoplegia / horizontal nystagmus Chronic Korsakoff: memory loss, confabulation, mammillary body atrophy; eye signs absent
36
Why does mammillary body atrophy cause memory deficits?
Mammillary bodies are part of the Papez circuit Damage → impaired hippocampus → mammillary body → anterior thalamus → cingulate gyrus pathway → anterograde amnesia
37
A patient on simvastatin develops muscle pain after starting erythromycin. Mechanism?
Erythromycin inhibits CYP3A4 → ↑ simvastatin levels → rhabdomyolysis Statins metabolized by CYP3A4: simvastatin, atorvastatin, lovastatin Safer alternatives: pravastatin, rosuvastatin
38
Patient receives ketamine for procedural sedation. Mechanism of action?
Noncompetitive NMDA receptor antagonist → blocks glutamate → dissociative anesthesia Effects: analgesia, amnesia, sedation Sympathomimetic: ↑ HR, BP, CO Minimal respiratory depression
39
Pseudopalisading necrosis, nuclear pleomorphism, microvascular proliferation in an adult brain tumor.
Glioblastoma multiforme (GBM) WHO Grade IV astrocytoma Most common in adults, usually frontal/temporal lobe Highly malignant, poor prognosis
40
“Fried-egg” cells and “chicken-wire” capillary pattern on histology; usually frontal lobe.
Oligodendroglioma Slow-growing, often frontal lobe Calcifications common Better prognosis than astrocytomas
41
Rosenthal fibers (eosinophilic corkscrew fibers) in a pediatric cerebellar tumor.
Pilocytic astrocytoma (WHO Grade I) Benign, slow-growing Most common in children, cerebellum Good prognosis with surgical resection
42
Homer Wright rosettes in a midline cerebellar tumor in a child.
Medulloblastoma Highly malignant, primitive neuroectodermal tumor (PNET) Common in children, midline cerebellum Can metastasize via CSF
43
Spindle-shaped cells in whorled pattern with psammoma bodies on histology.
Meningioma Extra-axial, slow-growing, often convexities, falx, sphenoid wing Usually benign, can cause mass effect
44
Perivascular pseudorosettes in a tumor lining the ventricles.
Ependymoma Often arises from 4th ventricle in children, spinal cord in adults Can cause hydrocephalus
45
A woman on metoclopramide develops secondary amenorrhea and galactorrhea. Mechanism?
Metoclopramide blocks D2 receptors → ↑ prolactin → inhibits GnRH → ↓ FSH/LH → anovulation → amenorrhea
46
A patient presents with left-sided numbness of the face and extremities, no motor deficits. Most likely lacunar infarct location?
Right thalamus (VPL/VPM) → pure sensory stroke Often due to small vessel disease (hypertension, diabetes)
47
Painless scrotal swelling that transilluminates, anterior to the testis.
Hydrocele Fluid between tunica vaginalis layers Transilluminates brightly Usually congenital in infants or acquired in adults
48
Painless mass superior/posterior to testis that may transilluminate.
Spermatocele Cyst in epididymal head containing sperm Transilluminates slightly opaque Usually asymptomatic
49
“Bag of worms” mass above testis, worse with standing/valsalva.
Varicocele (dilated pampiniform plexus) Does not transilluminate More common on left side (drains into left renal vein) Can cause infertility
50
A postmenopausal woman with osteoporosis and a history of DVT is seeking treatment. Which drug is safest?
Alendronate (bisphosphonate) ✅ Avoid: Estrogen, raloxifene ❌ (VTE risk) Testosterone only if male and hypogonadal
51
postmenopausal woman with osteoporosis has a history of deep vein thrombosis. She is now seeking treatment to reduce fracture risk. Which of the following medications is most appropriate for her? A. Alendronate B. Estrogen C. Lovastatin D. Raloxifene E. Testosterone
Answer: A. Alendronate ✅ Explanation: Alendronate: Safe first-line treatment for osteoporosis; reduces fracture risk. Estrogen & Raloxifene: Increase risk of venous thromboembolism → contraindicated in patients with prior DVT. Lovastatin: Not used for osteoporosis. Testosterone: Only indicated in men with hypogonadism.
52
Patient has thickened, white, flaking nails. Nail scrapings reveal elongated, pencil-shaped macroconidia and no microconidia. Etiologic agent?
Epidermophyton floccosum ✅ Club-shaped macroconidia, smooth-walled, multicellular Causes tinea pedis, tinea cruris, sometimes onychomycosis Unlike Trichophyton → no microconidia
53
A 3-year-old develops acute lower limb weakness after a viral illness. Where does the pathological agent primarily act?
Anterior horn cells ✅ Mechanism: virus infects motor neurons → flaccid paralysis Signs: hypotonia, hyporeflexia, asymmetric weakness Classic agent: poliovirus
54
A 1-month history of severe diarrhea is accompanied by perianal pain, fissures, scarring, sinus tracts, and fistulas. Most likely diagnosis?
Transmural inflammation Can affect any part of GI tract (skip lesions) Perianal disease common Differentiation from UC: UC → continuous mucosal disease, rarely perianal fistulas
55
A patient presents with fatigue, weakness, 8 lb weight loss, hypotension, hyponatremia, hyperkalemia, and elevated creatinine. Most likely diagnosis?
Primary adrenal insufficiency (Addison’s disease) ✅ Labs: ↓ Na⁺, ↑ K⁺, ↑ creatinine Mechanism: ↓ aldosterone → salt wasting; ↓ cortisol → hypotension, fatigue Causes: autoimmune (most common in developed countries), infections (TB in developing countries) Primary adrenal insufficiency (Addison’s disease): Destruction of adrenal cortex → ↓ cortisol & ↓ aldosterone ↓ Aldosterone → Na⁺ loss, K⁺ retention → hyponatremia, hyperkalemia ↓ Cortisol → hypotension, fatigue, weakness Can lead to prerenal acute kidney injury → ↑ creatinine
56
A patient has 3 weeks of lateral elbow pain, worse with tennis, radial head posterior, and pain with wrist extension. Mechanism?
Overuse of wrist extensors → microtears at lateral epicondyle (tennis elbow) ✅ Force transmitted to radial head → posterior pain/displacement Mechanism: repetitive wrist extension, especially backhand stroke
57
Uterus contains sharply circumscribed, discrete, round, firm, gray-white nodules ~5 cm. Most likely diagnosis?
Leiomyoma (uterine fibroid) ✅ Benign smooth muscle tumor of myometrium Usually firm, well-circumscribed, gray-white May cause menorrhagia, infertility, pelvic pressure
58
Woman with dysmenorrhea, menorrhagia, diffusely enlarged boggy uterus. Histology: endometrial glands in myometrium. Diagnosis?
Adenomyosis ✅
59
A patient uses an over-the-counter agent and develops flatulence, abdominal distention, and profuse diarrhea. Mechanism?
lactulose- Osmotic diarrhea due to non-absorbable sugar or magnesium salts ✅ Mechanism: solute in gut lumen draws water → diarrhea; bacterial fermentation → gas Common agents: lactulose, sorbitol, magnesium hydroxide
60
A patient starts prazosin for BPH and experiences dizziness and lightheadedness upon standing. Mechanism?
Alpha-1 blockade → vasodilation → impaired compensatory vasoconstriction → orthostatic hypotension ✅
61
12-year-old girl with heavy periods, purpura, epistaxis, gingival bleeding. Labs: normal platelet count, prolonged bleeding time. Diagnosis?
Glanzmann thrombasthenia (GPIIb/IIIa defect, impaired platelet aggregation) ✅
62
Boy with hemarthroses and muscle hematomas after minor trauma. Labs: prolonged aPTT, normal PT, normal platelets. Diagnosis?
: Hemophilia A (Factor VIII deficiency)
63
Two soldiers with neck scratches from civilian fur collars, develop pruritic papules → necrotic ulcers (black eschar), mild fever and malaise. Gram-positive aerobic rods seen. Most likely pathogen?
Bacillus anthracis (cutaneous anthrax) ✅ Exposure: contaminated animal hides/fur/wool Key features: painless necrotic eschar, mild systemic symptoms Gram stain: aerobic Gram-positive rods
64
Teenager with 2-month history of facial cysts and white papules after starting a new face wash. Histology shows what? A) Comedones filled with sebum and keratin B) Deposits of complements at the dermoepidermal junction C) Epidermal hyperplasia and koilocytes D) Microabscess E) Folliculitis
Classic for acne vulgaris Pathophysiology: follicular hyperkeratinization + sebum accumulation → comedone formation Other options: B → Lupus (dermoepidermal junction complement deposits) C → HPV/warts (koilocytes) D → Pustular bacterial lesions (not classic acne histology) E → Folliculitis (usually bacterial/fungal, not typical acne pattern)
65
23-year-old with memory loss, violent behavior, and hygiene neglect. You start pharmacologic therapy for Alzheimer’s. What is the mechanism of the first-line drugs?
B) Acetylcholinesterase inhibition ✅ Drugs: Donepezil, Rivastigmine, Galantamine Mechanism: increase acetylcholine in synaptic cleft → improve cognition and behavior NMDA blockade (Memantine) is second-line or adjunct Alzheimer’s pathology: Loss of basal forebrain cholinergic neurons, especially in the nucleus basalis of Meynert Leads to decreased acetylcholine (ACh) in the hippocampus and cortex Result: impaired memory, attention, and learning Role of acetylcholine: ACh is critical for cortical activation, memory formation, and attention Enhances synaptic plasticity in the hippocampus → facilitates encoding of new memories
65
Match the following reflexes to their spinal nerve roots: Biceps Brachioradialis Triceps
Biceps: C5 Brachioradialis: C6 Triceps: C7
66
A 75-year-old man presents with fatigue, weight loss, and RUQ tenderness. He previously worked in a plastic pipe factory. Liver biopsy shows pleomorphic spindle cells positive for PECAM-1 (CD31). What is the most likely diagnosis?
Hepatic angiosarcoma Hepatic angiosarcoma is a rare, aggressive vascular tumor of the liver associated with occupational exposure to vinyl chloride, arsenic, and Thorotrast (thorium dioxide). Tumor cells are of endothelial origin and express PECAM-1 (CD31).
67
What occupational and environmental exposures are classically associated with hepatic angiosarcoma?
Vinyl chloride (PVC industry, plastics) Arsenic (pesticides, contaminated water) Thorotrast (historical radiographic contrast) Explanation: These agents are potent carcinogens that induce endothelial mutations in hepatic sinusoids, leading to malignant vascular proliferation.
68
A rare, vascular, malignant tumor of the liver that is associated with exposure to ___
vinyl chloride, arsenic, and thorium dioxide.
69
An 84-year-old woman with an indwelling catheter and recurrent nephrolithiasis presents with confusion, fever, and alkaline urine (pH 8.5) that smells like ammonia. What organism is most likely responsible?
A: Proteus mirabilis Explanation: Gram-negative, oxidase-negative rod Urease-positive → splits urea into ammonia and CO₂ → alkalinizes urine (↑ pH) Ammonia odor in urine Promotes formation of struvite (magnesium ammonium phosphate) stones
70
How does Proteus mirabilis cause stone formation and alkaline urine?
Urease enzyme converts urea → ammonia + CO₂ Ammonia raises urinary pH Promotes precipitation of magnesium ammonium phosphate → struvite stones
71
What type of stones are associated with Proteus UTIs, and what are their characteristic features?
Struvite stones (magnesium ammonium phosphate) Radiopaque May form staghorn calculi Often require surgical removal due to recurrent infection and obstruction
72
11-year-old boy from Nigeria → Jaw mass + cervical lymphadenopathy → Biopsy: sheets of lymphocytes with tingible body macrophages (“starry sky” pattern) → EBV serology positive
✅ Answer: t(8;14) Diagnosis: Endemic (African) Burkitt lymphoma
73
Q: An 11-year-old boy from Nigeria presents with a jaw mass and EBV positivity. Biopsy shows a “starry sky” pattern. What is the diagnosis and associated translocation?
A: Diagnosis: Endemic Burkitt lymphoma Translocation: t(8;14) Gene: c-MYC (chromosome 8) translocated to Ig heavy chain locus (chromosome 14)
74
Q: What is the molecular consequence of the t(8;14) translocation in Burkitt lymphoma?
c-MYC oncogene on chromosome 8 becomes overexpressed due to its placement next to the immunoglobulin heavy-chain promoter on chromosome 14 Leads to uncontrolled cellular proliferation
75
A 72-year-old man has progressive lower extremity weakness, urinary incontinence, and back pain. Imaging shows multiple sclerotic (osteoblastic) lesions in the spine. What is the most likely underlying malignancy?
Metastatic prostate adenocarcinoma
76
A pregnant woman from South Asia presents with acute liver failure (jaundice, elevated transaminases, coagulopathy, encephalopathy). Which viral marker is most likely elevated?
A: Anti-HEV IgM Diagnosis: Acute Hepatitis E infection
77
What is the typical epidemiology of Hepatitis E virus (HEV)?
Transmission: Fecal–oral (contaminated water) Regions: Developing countries in Asia, Africa, Mexico Outbreaks: After heavy rains or poor sanitation
78
What type of virus is Hepatitis E?
Hepevirus family Non-enveloped, single-stranded, positive-sense RNA virus Replicates in the cytoplasm
79
A newborn with jaundice, anemia, splenomegaly, and echinocytes on blood smear most likely has a deficiency in what enzyme?
Pyruvate kinase deficiency → ↓ ATP production → membrane rigidity → extravascular hemolysis. Mnemonic: 💡 “PK = Power (ATP) Keeper” — without PK, RBCs lose power → rigid → splenic destruction. LDH leaks During Hemolysis” → L for Lactate, L for Leak, D for Destruction, H for Hemolysis.
80
What happens to LDH in hemolysis
LDH leaks During Hemolysis” → L for Lactate, L for Leak, D for Destruction, H for Hemolysis.
81
34-year-old archaeologist is concerned about premature skin aging from sun exposure. Which sunscreen ingredient provides broad-spectrum protection against both UVA and UVB radiation?
Zinc oxide (mineral-based sunscreen) Key points: UVA: penetrates deeper, causes photoaging and DNA damage UVB: causes sunburn and contributes to skin cancer Broad-spectrum sunscreens: zinc oxide, titanium dioxide → block both UVA & UVB Chemical UVB-only blockers: PABA, trolamine salicylate, cinnamates → do not prevent photoaging Mnemonic: 💡 “Zinc = Zenith of broad protection” → protects skin from both UVA and UVB.
82
: A 17-year-old presents with fever, sore throat, cervical lymphadenopathy, tonsillar exudates, palatal petechiae, and splenomegaly. Labs show lymphocytosis with atypical lymphocytes and a positive heterophile antibody test. Which condition is she at increased risk for?
Key points: Primary infection: Epstein-Barr virus (EBV) → infectious mononucleosis Symptoms: fever, pharyngitis, lymphadenopathy, splenomegaly, fatigue Labs: lymphocytosis, atypical lymphocytes, positive heterophile antibody Complications: Hematologic malignancies: Hodgkin lymphoma, Burkitt lymphoma, diffuse large B-cell lymphoma Nasopharyngeal carcinoma Mechanism: EBV latent infection → LMP1 activates NF-κB, driving B-cell proliferation Mnemonic: 💡 “EBV = Epstein’s Big Virus → Big risk for Hodgkin lymphoma”
83
Teardrop red blood cells
dacrocytes
84
A 65-year-old man presents with 6 months of fatigue and abdominal pain. Physical exam shows pallor and splenomegaly. Labs reveal Hb 9.1 g/dL, WBC 3,400/mm³. Peripheral smear shows teardrop cells and nucleated RBCs. Genetic testing is positive for a JAK2 mutation. Question: What is the most likely underlying mechanism of this patient’s condition?
Answer: Fibrosis in the bone marrow Explanation: This patient has primary myelofibrosis (PMF), a myeloproliferative neoplasm. Key features: Teardrop RBCs (from extramedullary hematopoiesis) Cytopenias (anemia, leukopenia) Splenomegaly (extramedullary hematopoiesis) JAK2 mutation → constitutive JAK-STAT activation Pathophysiology: Abnormal megakaryocytes release TGF-β and PDGF → marrow fibrosis Fibrosis disrupts normal hematopoiesis → blood cells produced in spleen/liver Other features: Fatigue, abdominal discomfort, risk of transformation to acute leukemia
85
2-month history of a cough productive of clear mucoid sputum. smoked one pack of cigarettes daily for 33 years. Chest x-ray shows a 2-cm solid nodule in the periphery of the lower left lobe. biopsy shows numerous mucin-filled epithelial cells lining the alveolar basement membrane. The cells have prominent nucleoli, coarse chromatin, and some cells have multiple nuclei. Which of the following is the most likely diagnosis?
adenocarcinoma of the lung Key USMLE points: Peripheral lung nodule in a smoker often adenocarcinoma Mucin-producing tumor with lepidic growth pattern Can present with clear sputum due to mucin production Prognosis better than small cell, worse if invasive features are present
86
_______ is a complication of untreated group A streptococcal (GAS) infections such as scarlet fever and tonsillopharyngitis. MR is the result of rheumatic heart disease, which can cause early mitral regurgitation or prolapse and later evolves into mitral stenosis.
Mitral valve regurgitation (MR)
87
A 23-year-old woman with asthma presents with severe shortness of breath and wheezing. She is unable to speak in full sentences. Vital signs: pulse 116/min, respirations 28/min, O₂ sat 92% on room air. Lung exam shows decreased breath sounds with scattered end-expiratory wheezing. She is started on high-dose continuous inhaled albuterol. Question: Which of the following adverse effects is she at increased risk for?
Hypokalemia Explanation: Mechanism: Albuterol is a β2-adrenergic agonist → stimulates Na⁺/K⁺-ATPase → shifts K⁺ into cells, causing hypokalemia. β2 stimulation also increases glycogenolysis → ↑ insulin → further drives K⁺ into cells. Other effects of high-dose β2-agonists: Tachycardia (β1 effect + reflex from vasodilation) Tremor Hypomagnesemia, hypophosphatemia Clinical importance: Hypokalemia can cause EKG changes: flattened T waves, ST depression, U waves Severe hypokalemia can precipitate arrhythmias Key USMLE Tip: Continuous or high-dose β2-agonist therapy increases risk for electrolyte disturbances, especially hypokalemia, even in otherwise healthy patients.
88
A 28-year-old woman comes to the emergency department because of a 2-day history of dark urine, increasing abdominal pain, and a tingling sensation in her arms and legs. She has a history of epilepsy. Her current medication is phenytoin. She is nauseated and confused. Following the administration of hemin and glucose, her symptoms improve. The beneficial effect of this treatment is most likely due to inhibition of which of the following enzymes? Aminolevulinate dehydratase Aminolevulinate acid synthase Ferrochelatase Porphobilinogen deaminase Uroporphyrinogen decarboxylase
ALA synthase Acute intermittent porphyria is treated with hemin + glucose, which inhibit ALA synthase, reducing the production of neurotoxic heme precursors ALA and PBG.
89
A 29-year-old woman, gravida 1, para 0 at 11 weeks' gestation comes to the physician because of a 2-day history of left lower extremity pain and swelling. Her temperature is 37.9°C (100.2°F). Physical examination shows a tender, palpable cord on the lateral aspect of the left lower leg. The overlying skin is erythematous and indurated. Duplex ultrasound shows vascular wall thickening and subcutaneous edema. Which of the following is the most likely diagnosis?
Superficial thrombophlebitis
90
A 35-year-old woman presents with acute right flank pain and gross hematuria. She has had similar episodes in the past. Urinalysis shows blood, and 24-hour urine collection reveals wedge-shaped crystals. Serum uric acid is mildly elevated. Which of the following is most likely to prevent recurrence? A. Low-potassium diet B. High-protein diet C. Amoxicillin/clavulanate D. Dietary calcium restriction E. Allopurinol F. Chlorthalidone
F. Chlorthalidone for te wedge shapes stones of the calcium phosphate
91
wedge shapes stones
calcium phosphate
92
A 60-year-old man comes to the physician because his wife has noticed that his left eye looks smaller than his right. He has had worsening left shoulder and arm pain for 3 months. He has smoked two packs of cigarettes daily for 35 years. Examination shows left-sided ptosis. The pupils are unequal but reactive to light; when measured in dim light, the left pupil is 3 mm and the right pupil is 5 mm. Which of the following is the most likely cause of this patient's ophthalmologic symptoms? Thrombosis of the cavernous sinus Aneurysm of the posterior cerebral artery Infarction of the hypothalamus Dissection of the carotid artery Compression of the stellate ganglion Infiltration of the cervical plexus
Compression of the stellate ganglion Compression of the stellate ganglion by a Pancoast tumor can lead to Horner syndrome via injury of preganglionic sympathetic fibers. Superior sulcus tumors can infiltrate neighboring structures and cause additional symptoms, which is known as Pancoast syndrome. This patient's shoulder and arm pain are likely symptoms of Pancoast syndrome, which also includes atrophy of the arm and hand muscles, and possibly superior vena cava syndrome and hoarseness due to compression of the recurrent laryngeal nerve. The most common cause of Pancoast syndrome is NSCLC, for which this patient is at risk because of his history of smoking.
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Compression of the Stellate ganglion
Horner syndrome (ipsilateral ptosis, miosis, anhidrosis)
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A 60-year-old woman comes to the physician because of palpitations and a 5.4-kg (11.9-lb) weight loss over the past 3 months. She appears anxious. Her pulse is 104/min and blood pressure is 148/101 mm Hg. Physical examination shows warm skin, mild tremor, and an enlarged thyroid gland. A thyroid scintigraphy scan shows several focal areas with increased uptake. A biopsy of one of these areas of affected thyroid tissue is most likely to show which of the following? A. Sheets of parafollicular cells with amyloid stroma B. Inflammatory infiltrate with multinucleated giant cells and granulomas C. Follicle destruction with lymphocytic infiltrate and germinal centers D. Patches of enlarged follicular cells distended with colloid E. Crowded follicular cells with scalloped colloid
D. Patches of enlarged follicular cells distended with colloid However, thyroid scintigraphy would show a diffuse uptake of radioactive iodine rather than the focal areas of increased uptake seen here. Furthermore, this patient is missing other classic signs of Graves disease such as ophthalmopathy and pretibial myxedema.
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A 12-year-old boy presents after a motor vehicle accident with acute left-sided chest pain, dyspnea, hypotension, tachycardia, distended neck veins, tracheal deviation to the right, hyperresonant left chest, and decreased breath sounds. Emergency needle decompression is indicated. What is the preferred site for needle insertion in a pediatric patient? A. 2nd intercostal space, midclavicular line B. 5th intercostal space, midaxillary line C. 8th intercostal space, posterior axillary line D. Subxiphoid space E. 5th intercostal space, midclavicular line
A. 2nd intercostal space, midclavicular line The 2nd left intercostal space along the midclavicular line is the recommended needle insertion site for emergency decompression of a tension pneumothorax in a child. The patient here is unstable with hypotension and tachycardia, so the pneumothorax should be decompressed as quickly as possible. Since the neurovascular bundle runs below each rib, the upper edge of the rib is the preferred puncture site to help mitigate the risk of excessive bleeding and nerve damage. Emergency needle thoracostomy should be followed by chest tube placement in the 5th intercostal space along the midaxillary line. According to the Advanced Trauma Life Support (ATLS) guidelines, the 2nd left intercostal space along the midclavicular line is no longer the preferred needle insertion site for emergency decompression of a tension pneumothorax in adults. This location is associated with high failure rates because of increased anterior chest wall thickness. Instead, placing the needle in the 5th left intercostal space along the midaxillary line is preferable.
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Does rheumatoid arthritis impact the DIP joints?
No! Osteoarthritis DIP and PIP.
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A 36-year-old woman, gravida 2, para 1, at 30 weeks' gestation comes to the physician for evaluation of increased urinary frequency. She has no history of major medical illness. Physical examination shows no abnormalities. Laboratory studies show an increased serum C-peptide concentration. Ultrasonography shows polyhydramnios and a fetus that is large for gestational age. Which of the following hormones is predominantly responsible for the observed laboratory changes in this patient? Estrogen Human placental lactogen Thyroxine Human chorionic gonadotropin Adrenocorticotropic hormone Progesterone
Human placental lactogen This patient presents with polyuria, polyhydramnios, a large-for-gestational-age fetus, and elevated maternal C-peptide at 30 weeks’ gestation, which are classic features of gestational diabetes mellitus (GDM). Key points: Human placental lactogen (hPL): Secreted by the syncytiotrophoblast of the placenta. Peaks in the third trimester. Causes maternal insulin resistance, ensuring glucose is available for the fetus. Leads to increased maternal insulin secretion, reflected as elevated C-peptide. Other hormones: Hormone Relevance Estrogen Supports uterine growth and blood flow, minor effect on insulin sensitivity Progesterone Maintains pregnancy, relaxes smooth muscle, minor metabolic effect hCG Peaks in first trimester, maintains corpus luteum, not responsible for insulin resistance Thyroxine Regulates metabolism, not a main driver of gestational hyperglycemia ACTH Stimulates cortisol, which can induce insulin resistance, but hPL is the predominant hormone in pregnancy-related insulin resistance Summary: Maternal hyperglycemia in late pregnancy → hPL-mediated insulin resistance Fetal effects: Increased glucose → macrosomia, polyhydramnios due to fetal polyuria Maternal labs: Compensatory hyperinsulinemia → elevated C-peptide USMLE-style mnemonic: “hPL = High sugar for the baby” → hPL induces maternal insulin resistance to supply glucose to the fetus.
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A 36-year-old woman at 30 weeks’ gestation presents with increased urinary frequency. Labs show elevated serum C-peptide, and ultrasound reveals polyhydramnios and a large-for-gestational-age fetus. Which hormone is primarily responsible for the maternal laboratory findings?
A. Estrogen B. Human placental lactogen C. Thyroxine D. Human chorionic gonadotropin E. Adrenocorticotropic hormone F. Progesterone Correct Answer: B. Human placental lactogen ✅ Explanation: Key features: Polyuria, polyhydramnios, macrosomia, elevated C-peptide → gestational diabetes mellitus. Human placental lactogen (hPL): Secreted by the placenta, induces maternal insulin resistance and beta-cell hyperplasia, increasing insulin and C-peptide. Ensures glucose availability for the fetus; maternal hyperglycemia → fetal hyperinsulinemia → macrosomia. Other hormones (estrogen, progesterone, hCG, thyroxine, ACTH) do not predominantly drive maternal hyperglycemia in late pregnancy. Mnemonic: “hPL = High sugar for the baby”