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A Rare Case of Subependymoma with an Atypical Presentation: A Case Report

A rare case of subependymoma in a young patient presenting with sensory dysesthesia is reported. Computed tomography scan and magnetic resonance imaging revealed a posterior fossa mass occluding the fourth ventricle with infiltration to the right side immediately behind the pontine tegmentum and imp...

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Autores principales: Kurukumbi, Mohankumar, Muley, Amruta, Ramidi, Ganga, Wynn, Zakiya, Trouth, Annapurni Jayam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223030/
https://www.ncbi.nlm.nih.gov/pubmed/22121350
http://dx.doi.org/10.1159/000333061
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author Kurukumbi, Mohankumar
Muley, Amruta
Ramidi, Ganga
Wynn, Zakiya
Trouth, Annapurni Jayam
author_facet Kurukumbi, Mohankumar
Muley, Amruta
Ramidi, Ganga
Wynn, Zakiya
Trouth, Annapurni Jayam
author_sort Kurukumbi, Mohankumar
collection PubMed
description A rare case of subependymoma in a young patient presenting with sensory dysesthesia is reported. Computed tomography scan and magnetic resonance imaging revealed a posterior fossa mass occluding the fourth ventricle with infiltration to the right side immediately behind the pontine tegmentum and impinging on the right spinothalamic tract. Postoperative tumor histopathology revealed the classical appearance of subependymoma. Subependymoma is a rare, asymptomatic, slow-growing, low-grade glioma of the central nervous system. If symptomatic, the clinical features are commonly secondary to hydrocephalus, but subependymoma presenting with sensory dysesthesia has never been reported in the literature.
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spelling pubmed-32230302011-11-25 A Rare Case of Subependymoma with an Atypical Presentation: A Case Report Kurukumbi, Mohankumar Muley, Amruta Ramidi, Ganga Wynn, Zakiya Trouth, Annapurni Jayam Case Rep Neurol Published: October, 2011 A rare case of subependymoma in a young patient presenting with sensory dysesthesia is reported. Computed tomography scan and magnetic resonance imaging revealed a posterior fossa mass occluding the fourth ventricle with infiltration to the right side immediately behind the pontine tegmentum and impinging on the right spinothalamic tract. Postoperative tumor histopathology revealed the classical appearance of subependymoma. Subependymoma is a rare, asymptomatic, slow-growing, low-grade glioma of the central nervous system. If symptomatic, the clinical features are commonly secondary to hydrocephalus, but subependymoma presenting with sensory dysesthesia has never been reported in the literature. S. Karger AG 2011-10-01 /pmc/articles/PMC3223030/ /pubmed/22121350 http://dx.doi.org/10.1159/000333061 Text en Copyright © 2011 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No-Derivative-Works License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published: October, 2011
Kurukumbi, Mohankumar
Muley, Amruta
Ramidi, Ganga
Wynn, Zakiya
Trouth, Annapurni Jayam
A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title_full A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title_fullStr A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title_full_unstemmed A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title_short A Rare Case of Subependymoma with an Atypical Presentation: A Case Report
title_sort rare case of subependymoma with an atypical presentation: a case report
topic Published: October, 2011
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223030/
https://www.ncbi.nlm.nih.gov/pubmed/22121350
http://dx.doi.org/10.1159/000333061
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