SDHx mutations are associated with the PI3K-Akt signaling pathway in vagal paragangliomas

Background: Vagal paraganglioma (VPGL) is a very rare neuroendocrine tumor arising from the paraganglion associated with the vagus nerve. VPGL is mainly characterized by an asymptomatic course and slow growth. However, up to 19% of tumors can metastasize. Due to the rarity of this tumor, information...

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Main Authors: Snezhkina Anastasiya V., Fedorova Maria S., Ayupova Asiya F., Pudova Elena A., Kobelyatskaya Anastasiya A., Kalinin Dmitry V., Golovyuk Alexander L., Krasnov George S., Pavlov Vladislav S., Kudryavtseva Anna V.
Format: Article
Language:English
Published: Institute of Oncology, Sremska Kamenica, Serbia 2023-01-01
Series:Archive of Oncology
Subjects:
Online Access:https://scindeks-clanci.ceon.rs/data/pdf/0354-7310/2023/0354-73102302004S.pdf