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Journal of the Korean Surgical Society ; : 287-290, 2009.
Artigo em Coreano | WPRIM | ID: wpr-207828

RESUMO

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.


Assuntos
Humanos , Carcinoma de Células Renais , Sistema Nervoso Central , Cistadenoma Seroso , Genes Supressores de Tumor , Mutação em Linhagem Germinativa , Tumores Neuroendócrinos , Cisto Pancreático , Feocromocitoma , Doença de von Hippel-Lindau
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