Pheochromocytoma: an updated scoping review from clinical presentation to management and treatment

Pheochromocytoma: an updated scoping review from clinical presentation to management and treatment

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors derived from chromaffin cells, with 80–85% originating in the adrenal medulla and 15–20% from extra-adrenal chromaffin tissues (paragangliomas). Approximately 30–40% of PPGLs have a hereditary component, making them one of t...

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Bibliographic Details
Main Authors: J. S. Saavedra T., Humberto Alejandro Nati-Castillo, L. A. Valderrama Cometa, Wilfredo A. Rivera-Martínez, Josué Asprilla, C. M. Castaño-Giraldo, Leonardo Sánchez S., Mishell Heredia-Espín, Marlon Arias-Intriago, Juan S. Izquierdo-Condoy
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Endocrinology
Subjects:
pheochromocytoma
paraganglioma
hormonal imbalance
diagnosis
management
treatment
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2024.1433582/full

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https://www.frontiersin.org/articles/10.3389/fendo.2024.1433582/full

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