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Journal of the Korean Surgical Society ; : 287-290, 2009.
Article in Korean | WPRIM | ID: wpr-207828

ABSTRACT

The von Hippel-Lindau (VHL) disease is an autosomal dominant disorder by germline mutation of VHL tumor suppressor gene. The affected patients mainly develop cancers of the central nervous system, renal cell carcinoma, pheochromocytoma, and pancreatic cysts. Pancreatic involvement was observed 12~77% in VHL patients and included true cysts, serous cystadenomas, and neuroendocrine tumors. We experienced two cases of pancreatic cyst of the von Hippel-Lindau disease and reviewed associated literatures.


Subject(s)
Humans , Carcinoma, Renal Cell , Central Nervous System , Cystadenoma, Serous , Genes, Tumor Suppressor , Germ-Line Mutation , Neuroendocrine Tumors , Pancreatic Cyst , Pheochromocytoma , von Hippel-Lindau Disease
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