Synchronous Presentation of Rare Brain Tumors in Von Hippel–Lindau Syndrome

Synchronous Presentation of Rare Brain Tumors in Von Hippel–Lindau Syndrome

Von Hippel–Lindau (VHL) disease is a heritable cancer syndrome in which benign and malignant tumors and/or cysts develop throughout the central nervous system (CNS) and visceral organs. The disease results from mutations in the VHL tumor suppressor gene located on chromosome 3 (3p25-26). A majority...

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Manylion Llyfryddiaeth
Prif Awduron: Mariachiara Lodi, Antonio Marrazzo, Antonella Cacchione, Marina Macchiaiolo, Antonino Romanzo, Luciano Mastronardi, Francesca Diomedi-Camassei, Alessia Carboni, Andrea Carai, Carlo Gandolfo, Lidia Monti, Angela Mastronuzzi, Giovanna Stefania Colafati
Fformat: Erthygl
Iaith:English
Cyhoeddwyd: MDPI AG 2021-05-01
Cyfres:Diagnostics
Pynciau:
hemangioblastomas
endolymphatic sac tumor
MRI
Von Hippel–Lindau syndrome
Mynediad Ar-lein:https://www.mdpi.com/2075-4418/11/6/1005

Rhyngrwyd

https://www.mdpi.com/2075-4418/11/6/1005

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