A case report highlights atypical presentation of MEN2A syndrome with implications for surgical management and surveillance.
MEN2A may present with bilateral pheochromocytoma a decade before medullary thyroid carcinoma. This case highlights that high‐risk RET mutations must dictate surgical management regardless of benign cytology. Furthermore, it underscores the necessity of lifelong surveillance for late adrenal recurrences presenting as hypertensive crises.
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Vallejo-Soto et al. (2026) studied this question.
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