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Case Report
A Case of von Hippel–Lindau Disease with Colorectal Adenocarcinoma, Renal Cell Carcinoma and Hemangioblastomas
Su Jin Heo, Choong-kun Lee, Kyu Yeon Hahn, Gyuri Kim, Hyuk Hur, Sung Hoon Choi, Kyung Seok Han, Arthur Cho, Minkyu Jung
Cancer Res Treat. 2016;48(1):409-414.   Published online February 17, 2015
DOI: https://doi.org/10.4143/crt.2014.299
AbstractAbstract PDFPubReaderePub
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 malignant tumors in the central nervous system (CNS) and the internal organs, including kidney, adrenal gland, and pancreas. We herein describe the case of a 74-year-old man carrying the VHL gene mutation who was affected by simultaneous colorectal adenocarcinoma, renal clear cell carcinoma, and hemangioblastomas of CNS.

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  • Sporadic Renal Hemangioblastoma: A Case Report of a Rare Entity
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    Cureus.2023;[Epub]     CrossRef
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    World Neurosurgery.2021; 150: e696.     CrossRef
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  • MicroRNA Assisted Gene Regulation in Colorectal Cancer
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    International Journal of Molecular Sciences.2019; 20(19): 4899.     CrossRef
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