A Case of von Hippel–Lindau Disease with Colorectal Adenocarcinoma, Renal Cell Carcinoma and Hemangioblastomas

von Hippel–Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome associated with mutations of the VHL tumor suppressor gene located on chromosome 3p25. The loss of functional VHL protein contributes to tumorigenesis. This condition is characterized by development of benign and malig...

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Bibliographic Details
Published in:Cancer Res Treat
Main Authors: Heo, Su Jin, Lee, Choong-kun, Hahn, Kyu Yeon, Kim, Gyuri, Hur, Hyuk, Choi, Sung Hoon, Han, Kyung Seok, Cho, Arthur, Jung, Minkyu
Format: Artigo
Language:Inglês
Published: Korean Cancer Association 2016
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4720105/
https://ncbi.nlm.nih.gov/pubmed/25715769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4143/crt.2014.299
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