Germline VHL Mutation Discovered in Association with EGFR-Positive Lung Cancer and Metachronous Hepatocellular Carcinoma: A Case Report
VHL is a tumor suppressor gene located on chromosome 3 that is classically associated with tumors of the eye and CNS, renal cell carcinoma, and pheochromocytoma. We describe what appears to be the first report of an association between a germline VHL mutation and non-small cell lung cancer and metac...
Main Authors: | Justin J. Kuhlman, Quinn J. Frier, Daniel Sumarriva, Matthew Oberley, Danielle Bolton, Ruby A. Deveras |
---|---|
Format: | Article |
Language: | English |
Published: |
Karger Publishers
2021-09-01
|
Series: | Case Reports in Oncology |
Subjects: | |
Online Access: | https://www.karger.com/Article/FullText/518318 |
Similar Items
-
Identification of Somatic Mutations in the von Hippel–Lindau (VHL) Gene in a Patient With Renal Cell Carcinoma
by: Wen-Chung Wang, et al.
Published: (2009-11-01) -
Von Hippel–Lindau Disease (VHL): Characteristic Lesions with Classic Imaging Findings
by: Suryansh Bajaj, et al.
Published: (2023-08-01) -
A Narrative Review of Pheochromocytoma in VHL
by: Danilo Coco, et al.
Published: (2024-02-01) -
Loss of VHL in RCC reduces repair and alters cellular response to benzo[a]pyrene
by: Marten eSchults, et al.
Published: (2013-10-01) -
9º Simpósio Médico Internacional de VHL; III Encontro de Famílias com a Síndrome de VHL Data:
by: Instituto Nacional de Câncer José de Alencar Gomes da Silva
Published: (2010-06-01)