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Indian J Pathol Microbiol ; 2003 Jul; 46(3): 482-3
Article in English | IMSEAR | ID: sea-74596

ABSTRACT

Von Hippel Lindau (VHL) disease is a rare autosomal dominant condition manifested by central nervous system hemangioblastoma, retinal angiomas, cysts of pancreas, kidney and epididymis, pheochromocytomas and renal cell carcinoma. We present such a case in a 45 years old male patient.


Subject(s)
Carcinoma, Renal Cell/pathology , Hemangioblastoma/pathology , Humans , Kidney Neoplasms/pathology , Male , Middle Aged , Supratentorial Neoplasms/pathology , von Hippel-Lindau Disease/pathology
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