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Hereditary and clinical insights into paraganglioma and pheochromocytoma

Background: Approximately 30–40% of paragangliomas (PGLs) and pheochromocytomas (PCCs) harbor an underlying hereditary cause. Early identification of at-risk individuals is imperative given the early onset, aggressiveness of tumors, and other tumor/cancer risks associated with hereditary PGLs/PCCs....

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Principais autores: Caitlin B Mauer Hall, Elise M Watson, Tanushree Prasad, Chandler L Myers, Jacqueline A Mersch
Format: Artigo
Sprog:Inglês
Udgivet: Bioscientifica 2024-11-01
Serier:Endocrine Oncology
Fag:
hereditary predisposition
incidental findings
paraganglioma
pheochromocytoma
sdhx
Online adgang:https://eo.bioscientifica.com/view/journals/eo/4/1/EO-24-0029.xml
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