๐จ A 68-year-old man with hypertension and CKD is admitted for community-acquired pneumonia.
On hospital day 3 he develops acute pleuritic chest pain and dyspnea.
Vitals: HR 118, BP 138/82, RR 26, Oโ sat 92% on 4L NC.
Labs:
* D-dimer markedly elevated
* Troponin mildly elevated
* BNP elevated
* Cr 2.8 mg/dL (baseline 1.9)
=> What is the most likely diagnosis?
=> What's the appropriate next step?
A 32-year-old pregnant female at 28 weeks gestation comes in for routine prenatal visit. She has type 1 diabetes mellitus.
Her self-monitoring blood glucose logs show:
* Fasting: 90 โ 95 mg/dL
* 1 hour postprandial: 130 โ 140 mg/dL
However, her lab HbA1c is reported as 4.8%.
The physician also notes she has homozygous sickle cell anemia (HbSS).
Which of the following laboratory markers would provide the most accurate assessment of her glycemic control over the past 2 โ 3 weeks?
A) Fasting plasma glucose
B) Fructosamine
C) HbA1c repeat test
D) OGTT
E) Urine ketones
Explain your answer in the comment section.
Why not the others?
A. Adenosine deaminase => SCID
B. Glucose-6-phosphatase => Von Gierke disease
D. Xanthine oxidase deficiency => Xanthinuria (low uric acid, not gout)
Answer: C. HGPRT
=> The combination of developmental delay, self-mutilation (lip/finger biting), hyperuricemia, and gout is classic for Lesch-Nyhan syndrome.
=> Lesch-Nyhan syndrome is caused by deficiency of Hypoxanthine-Guanine Phosphoribosyltransferase (HGPRT), a purine salvage enzyme.
=> Loss of HGPRT leads to increased purine degradation and excess uric acid production, causing gout and neurologic manifestations.
Answer: B. Severe Combined Immunodeficiency (SCID)
=> The thymus is the site of T-cell maturation, so an absent thymic shadow suggests a profound T-cell deficiency.
=> SCID is characterized by severe defects in both T-cell and B-cell function, leading to severe lymphopenia and recurrent infections early in life.
=> On chest X-ray, infants with SCID often have an absent thymic shadow due to lack of normal thymic development.
An absent thymic shadow on a newborn X-ray combined with severe lymphopenia indicates which defect?
A. Bruton agammaglobulinemia
B. Severe combined immunodeficiency (SCID)
C. Chronic granulomatous disease
D. C5-C9 complement deficiency
@_uakbar โ Correct
Diffuse concave ST elevation + PR depression = pericarditis until proven otherwise.
Whatโs the most common cause of pericarditis in a young healthy patient vs an older one?
Which condition characteristically presents with diffuse ST-segment elevations and PR-segment depressions on ECG?
A. Acute myocardial infarction
B. Acute pericarditis
C. Pulmonary embolism
D. Dilated cardiomyopathy
@ajlkfad2333 โ Correct
Diffuse concave ST elevation + PR depression = pericarditis until proven otherwise.
Whatโs one ECG finding that would make you worry about tamponade instead?
๐จ HIV patient, CD4 80.
Fever, dry cough, exertional dyspnea.
BAL silver stain shows disc-shaped cysts.
First-line treatment?
A. Azithromycin
B. Ganciclovir
C. Trimethoprim-sulfamethoxazole
D. Fluconazole
Answer With Reasons
@Chiragrx07 Exactly right @Chiragrx07
In classic PCP, TMP-SMX is first-line.
Donโt forget steroids in hypoxic patients.
What would you switch to if allergic to sulfa?