The clinical presentation—episodic hypertension with classic triad of headache, sweating, and palpitations—combined with elevated plasma metanephrines strongly suggests pheochromocytoma. Once biochemical diagnosis is confirmed, anatomical localization is the next critical step.
Contrast-enhanced CT can differentiate pheochromocytoma from benign adrenal adenoma by assessing washout characteristics (pheochromocytomas retain contrast longer). Always obtain imaging before any invasive procedure (biopsy, angiography) to avoid catecholamine release.
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