Current prospects of hereditary adrenal tumors: towards better clinical management

Abstract Adrenocortical carcinoma (ACC) and pheochromocytoma/paraganglioma (PPGL) are two rare types of adrenal gland malignancies. Regarding hereditary tumors, some patients with ACC are associated with with Li-Fraumeni syndrome (LFS), and those with PPGL with multiple endocrine neoplasia type 2. R...

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Bibliographic Details
Main Authors: Akihiro Ohmoto, Naomi Hayashi, Shunji Takahashi, Arisa Ueki
Format: Article
Language:English
Published: BMC 2024-03-01
Series:Hereditary Cancer in Clinical Practice
Subjects:
Online Access:https://doi.org/10.1186/s13053-024-00276-6