Question:
A 45-year-old woman presents with episodic palpitations, headache, and sweating. On examination, her blood pressure is 180/110 mmHg, and she has tachycardia. Laboratory tests reveal elevated plasma metanephrines. What is the most likely diagnosis?
Options:
A. Hyperthyroidism
B. Essential hypertension
C. Pheochromocytoma
D. Cushing’s syndrome
✅ Answer: C. Pheochromocytoma
Explanation:
Clinical triad: episodic headache, palpitations, and sweating are classic for pheochromocytoma, a catecholamine-secreting tumor of the adrenal medulla.
Paroxysmal hypertension is common; sustained hypertension may also be seen.
Lab findings: elevated plasma or urinary metanephrines confirm catecholamine excess.
Differential diagnosis:
Hyperthyroidism → palpitations, tachycardia, weight loss, heat intolerance; usually no episodic severe hypertension.
Essential hypertension → chronic, not paroxysmal; no catecholamine excess.
Cushing’s syndrome → features include central obesity, moon face, striae, hypokalemia, but not paroxysmal hypertension.
Imaging: CT or MRI of adrenal glands helps locate the tumor.
Management:
Preoperative alpha-blockade (e.g., phenoxybenzamine) followed by beta-blockade for tachycardia.
Surgical adrenalectomy is definitive treatment.
Complications if untreated: hypertensive crisis, arrhythmias, myocardial infarction, stroke.
References: Harrison’s Principles of Internal Medicine, 21st Edition, Ch. 230;
UpToDate: Pheochromocytoma and paraganglioma.
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