A 42-Year-Old Woman Presenting With Pheochromocytoma Multisystem Crisis Associated With Bilateral Pheochromocytomas Due to Multiple Endocrine Neoplasia Type 2A
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BACKGROUND Multiple endocrine neoplasia type 2A (MEN 2A) is a rare autosomal-dominant genetic syndrome characterized by mutations in the RET gene and tumors of endocrine glands, including pheochromocytomas. Pheochromocytoma is a benign primary endocrine tumor ... ...
