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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Autors principals:	Caitlin B Mauer Hall, Elise M Watson, Tanushree Prasad, Chandler L Myers, Jacqueline A Mersch
Format:	Artigo
Idioma:	Inglês
Publicat:	Bioscientifica 2024-11-01
Col·lecció:	Endocrine Oncology
Matèries:	hereditary predisposition incidental findings paraganglioma pheochromocytoma sdhx
Accés en línia:	https://eo.bioscientifica.com/view/journals/eo/4/1/EO-24-0029.xml
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