Pheochromocytoma-paraganglioma type 5 syndrome associated with mutation in the succinate dehydrogenase type A complex (SDHA), a case report

Pheochromocytomas and paragangliomas are rare neuroendocrine neoplasms that can produce catecholamines, with an incidence of less than one case per million inhabitants. They are histologically benign and minimally different from their malignant counterparts. The most common mutation is in the succin...

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Bibliographic Details
Main Authors: Myriam Vanessa Rueda-Galvis, Alejandro Román-Gonzaléz, Valentina Agredo-Delgado
Format: Article
Language:Spanish
Published: Universidad de Antioquia 2023-01-01
Series:Iatreia
Subjects:
Online Access:https://revistas.udea.edu.co/index.php/iatreia/article/view/348587/20809292