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Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature

Supratentorial hemangioblastomas (HBLs) are rare, benign vascular tumors of the central nervous system neoplasms. Very scarce literature is available regarding supratentorial HBL without von Hippel–Lindau (VHL) syndrome in an adult. We reviewed the literature and PubMed advanced search showed only a...

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Autores principales: Pandey, Sharad, Sharma, Vivek, Pandey, Deepa, Kumar, Vikul, Kumar, Mohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732265/
https://www.ncbi.nlm.nih.gov/pubmed/26889272
http://dx.doi.org/10.4103/1793-5482.165782
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author Pandey, Sharad
Sharma, Vivek
Pandey, Deepa
Kumar, Vikul
Kumar, Mohan
author_facet Pandey, Sharad
Sharma, Vivek
Pandey, Deepa
Kumar, Vikul
Kumar, Mohan
author_sort Pandey, Sharad
collection PubMed
description Supratentorial hemangioblastomas (HBLs) are rare, benign vascular tumors of the central nervous system neoplasms. Very scarce literature is available regarding supratentorial HBL without von Hippel–Lindau (VHL) syndrome in an adult. We reviewed the literature and PubMed advanced search showed only a few results of supratentorial HBL without VHL syndrome. We reported a rare case of cystic supratentorial HBL in 39-year-old male affecting the parietal lobe without VHL syndrome. Supratentorial HBL is a rare tumor and supratentorial HBL without VHL syndrome are even rarer. Being a rare entity, not much clinical data is currently available regarding supratentorial HBLs, thus necessitating the need for further reporting and review of such cases.
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spelling pubmed-47322652016-02-17 Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature Pandey, Sharad Sharma, Vivek Pandey, Deepa Kumar, Vikul Kumar, Mohan Asian J Neurosurg Review Article Supratentorial hemangioblastomas (HBLs) are rare, benign vascular tumors of the central nervous system neoplasms. Very scarce literature is available regarding supratentorial HBL without von Hippel–Lindau (VHL) syndrome in an adult. We reviewed the literature and PubMed advanced search showed only a few results of supratentorial HBL without VHL syndrome. We reported a rare case of cystic supratentorial HBL in 39-year-old male affecting the parietal lobe without VHL syndrome. Supratentorial HBL is a rare tumor and supratentorial HBL without VHL syndrome are even rarer. Being a rare entity, not much clinical data is currently available regarding supratentorial HBLs, thus necessitating the need for further reporting and review of such cases. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4732265/ /pubmed/26889272 http://dx.doi.org/10.4103/1793-5482.165782 Text en Copyright: © Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Review Article
Pandey, Sharad
Sharma, Vivek
Pandey, Deepa
Kumar, Vikul
Kumar, Mohan
Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title_full Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title_fullStr Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title_full_unstemmed Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title_short Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
title_sort supratentorial haemangioblastoma without von hippel–lindau syndrome in an adult: a rare tumor with review of literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732265/
https://www.ncbi.nlm.nih.gov/pubmed/26889272
http://dx.doi.org/10.4103/1793-5482.165782
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