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#3231 Minimally invasive cortical sparing adrenal surgery in the treatment of pheochromocytomas in multiple endocrine neoplasia type 2

Introduction: Pheochromocytoma is a neuroendocrine tumor originating from chromaffin cells of the adrenal medulla. Over 30% of pheochromocytomas are associated with mutations in germ line cells including rearranged in transfection mutations observed in multiple endocrine neoplasia type 2 syndromes. MEN2 associated pheochromocytoma is more likely to be bilateral and benign.

Conference: 18th Annual ENETS Concerence (2021)

Presenting Author:

Authors: Yiannakopoulou E,

Keywords: pheochromocytoma, adrenal sparing surgery, MEN2,