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- W2105158630 abstract "Haemangioblastoma, a benign vascular tumor derived from the capillary of endothelial cells, is an inherited disorder due to an autosomal dominant trait. The prevalence rates accounted for 1% to 2.5% of all intracranial tumors and 2% to 3% of all intramedullary spinal cord tumors. We report the infrequent case of a robust allegation of von Hippel-Lindau (VHL) associated haemangioblastoma in the central nervous system of a man. A 20 years old male presented to the hospital with the chief complaint of progressive chronic cephalgia three months prior to hospitalization. He complained also of blurred vision on neurologic examination; there is papilla edema with suspicion of retinal edema. Radiological examination result suggested a cerebellar haemangioblastoma dextra with noncommunicating hydrocephalus. After the first operation (installation of VP shunting) and subsequent operation (excision of the tumor), the pathological anatomy results revealed a cavernous angioma." @default.
- W2105158630 created "2016-06-24" @default.
- W2105158630 creator A5055679393 @default.
- W2105158630 date "2014-01-01" @default.
- W2105158630 modified "2023-09-24" @default.
- W2105158630 title "A Robust Allegation of Von Hippel-Lindau (VHL) Associated Hemangioblastoma in the Central Nervous System (CNS): A Case Report" @default.
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- W2105158630 doi "https://doi.org/10.11648/j.ijmi.20140201.11" @default.
- W2105158630 hasPublicationYear "2014" @default.
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