Treatment of recurrent cerebellar hemangioblastoma with external radiotherapy in a patient with von Hippel-Lindau disease: a case report and review of the literature.

Abstract:

:Von Hippel-Lindau Disease, a multisystem familial cancer syndrome, is inherited as an autosomal-dominant trait. Common manifestations of the disease are retinal, cerebellar and medullary hemangioblastomas; renal cysts and carcinomas; pancreatic cysts; pheochromocytoma; and papilllary cystadenoma of the epididym. We report the case of a 40-year-old man with type I von Hippel-Lindau disease treated with external radiotherapy for recurrent cerebellar hemangioblastoma.

journal_name

J Neurooncol

authors

Ertas G,Altundag MB,Ucer AR,Cankal F,Altundag K

doi

10.1007/s11060-004-5179-0

subject

Has Abstract

pub_date

2005-07-01 00:00:00

pages

273-5

issue

3

eissn

0167-594X

issn

1573-7373

journal_volume

73

pub_type

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