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A Case of von Hippel-Lindau Disease with Colorectal Adenocarcinoma, Renal Cell Carcinoma and Hemangioblastomas / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment ; : 409-414, 2016.
Article in English | WPRIM | ID: wpr-20749
ABSTRACT
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pancreas / Carcinoma, Renal Cell / Colorectal Neoplasms / Adenocarcinoma / Central Nervous System / Genes, Tumor Suppressor / Adrenal Glands / Hemangioblastoma / Carcinogenesis / Von Hippel-Lindau Disease Limits: Aged / Humans Language: English Journal: Cancer Research and Treatment Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pancreas / Carcinoma, Renal Cell / Colorectal Neoplasms / Adenocarcinoma / Central Nervous System / Genes, Tumor Suppressor / Adrenal Glands / Hemangioblastoma / Carcinogenesis / Von Hippel-Lindau Disease Limits: Aged / Humans Language: English Journal: Cancer Research and Treatment Year: 2016 Type: Article