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...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | Russian |
Published: |
Endocrinology Research Centre
2018-07-01
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Series: | Эндокринная хирургия |
Subjects: | |
Online Access: | https://surg-endojournals.ru/serg/article/viewFile/9731/7278 |