Haemangioblastoma, Haemangioblastomatosis, and von Hippel-Lindau Disease

Resche, F; Moisan, Jean‐Paul; Mantoura, J.; Kersaint-Gilly, A. De; Andre, March; Perrin-Resche, I.; Menegalli-Boggelli, D.; Lajat, Y; Richard, Stéphane

doi:10.1007/978-3-7091-6912-4_6

Cited by 93 publications

(69 citation statements)

References 261 publications

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“…This tumor is one of the rarest tumours of the CNS which accounts for about 2 % of the entire CNS tumor and about 7.5 % of all and 5 % in spinal [11]. Haemangiblastoma was usually associated with VHL disease.…”

Section: Discussionmentioning

confidence: 99%

A Robust Allegation of Von Hippel-Lindau (VHL) Associated Hemangioblastoma in the Central Nervous System (CNS): A Case Report

Amran¹

2014

IJMI

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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.

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Section: Discussionmentioning

confidence: 99%

A Robust Allegation of Von Hippel-Lindau (VHL) Associated Hemangioblastoma in the Central Nervous System (CNS): A Case Report

Amran¹

2014

IJMI

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“…10,11,13) Therefore, the persistent PHA is the main or exclusive feeder of the posterior circulation. Temporary clamping of the persistent PHA during CEA may increase the risk of ischemia.…”

Section: Discussionmentioning

confidence: 99%

“…6) Some clinical symptoms associated with the persistent PHA include hypoglossal nerve palsy, as well as neuralgia of the glossopharyngeal nerve due to irritation by the large persistent PHA. 1,3,13) However, the persistent PHA is mostly found incidentally at angiographic evaluation. Although conventional angiography is considered the standard of reference when evaluating vascular structures, MR and 3D-CT angiography are noninvasive alternatives that have some advantages.…”

Section: Discussionmentioning

confidence: 99%

Rare Variant of Persistent Primitive Hypoglossal Artery, Arising From the External Carotid Artery

Nanto

Takado

Ohbuchi

et al. 2012

Neurol. Med. Chir.(Tokyo)

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A 63-year-old man presented with an extremely rare variant of persistent primitive hypoglossal artery (PHA), which was found incidentally during examination for a contralateral asymptomatic internal carotid artery (ICA) stenosis. This anastomotic vessel arose from the external carotid artery, not the ICA, and joined the vertebrobasilar artery through the hypoglossal canal. Persistent PHA is rare and the reported incidence is 0.027-0.26%. Recognition of the existence of this variant vessel and preservation during neuroradiologic intervention or surgery is important to prevent possible ischemic complications.

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“…Rosen, Lamiell and colleagues, and Resche and colleagues ) [4][5][6] . In 1872, Jackson first described a cerebellar haemangioblastoma, and retinal haemangioblastoma was described by Panas and Rémy in 1879 1 .…”

Section: Introductionmentioning

confidence: 99%