Personalized diagnostics of chromaffin tumors (pheochromocytoma, paraganglioma) in oncoendocrinology

Pheochromocytomas and paragangliomas (PPGLs) are rare catecholamine-secreting neuroendocrine tumours, up to 40% of which occur in the setting of a hereditary syndrome. The incidence is 2 to 8 per million persons per year. The peak incidence occurs in the third to fifth decades of life. According to...

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Main Authors: Pavel O. Rumyantsev, Diana R. Yazykova, Konstantin Y. Slashchuk, Mikhail V. Degtyarev, Valentina S. Yasyuchenya, Sergey S. Serzhenko, Marina S. Sheremeta, Ivan I. Dedov
Format: Article
Language:Russian
Published: Endocrinology Research Centre 2018-07-01
Series:Эндокринная хирургия
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Online Access:https://surg-endojournals.ru/serg/article/viewFile/9731/7278