| Literature DB >> 9675924 |
J A Gallego Sánchez1, J G Pereira Arias, J Larrinaga Simón, A Astobieta Odriozola, N Prieto Ugidos, J G Ibarlucea González, C Bernuy Malfaz.
Abstract
Von Hippel Lindau disease is a highly uncommon autosomic dominant condition characterised by the presence of cerebellar hemangioblastomas, retina angioma, pancreas, kidney and epididymal cysts, and renal cells carcinoma. This article describes the case report of a male patient with Von Hippel Lindau disease which presented as a jaundice secondary to biliary obstruction due to pancreatic cystic mass. After urological examination, bilateral cystic lesions and right renal solid lesion were detected requiring surgical treatment. A review is made of the diagnostic and therapeutic aspects, highlighting the significance of early diagnosis and treatment.Entities:
Mesh:
Year: 1998 PMID: 9675924
Source DB: PubMed Journal: Actas Urol Esp ISSN: 0210-4806 Impact factor: 0.994