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Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review

Myxopapillary ependymoma (MPE) is a histological variant of ependymoma found in the conus medullaris or filum terminale region. Intracranial occurrence of the tumor is a rarity. The most characteristic histological feature of myxopapillary tumors is the abundance of intercellular and perivascular mu...

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Autores principales: Mewada, Tushit Bharat, Bishnoi, Ishu Hetram, Singh, Hukum, Singh, Daljit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652108/
https://www.ncbi.nlm.nih.gov/pubmed/29114296
http://dx.doi.org/10.4103/ajns.AJNS_45_15
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author Mewada, Tushit Bharat
Bishnoi, Ishu Hetram
Singh, Hukum
Singh, Daljit
author_facet Mewada, Tushit Bharat
Bishnoi, Ishu Hetram
Singh, Hukum
Singh, Daljit
author_sort Mewada, Tushit Bharat
collection PubMed
description Myxopapillary ependymoma (MPE) is a histological variant of ependymoma found in the conus medullaris or filum terminale region. Intracranial occurrence of the tumor is a rarity. The most characteristic histological feature of myxopapillary tumors is the abundance of intercellular and perivascular mucin and the arborizing vasculature, which tends to form papillae. We are reporting a 14-year-old patient presented with seizures caused by the right occipital region intraparenchymal lesion. Histopathology confirmed it to be MPE. Lesion was excised completely. Literature reviews on the topic are discussed regarding the histological findings, natural history, and outcome of surgically treated MPE. This is the fifth reported case of cerebral intraparenchymal primary MPE.
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spelling pubmed-56521082017-11-07 Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review Mewada, Tushit Bharat Bishnoi, Ishu Hetram Singh, Hukum Singh, Daljit Asian J Neurosurg Case Report Myxopapillary ependymoma (MPE) is a histological variant of ependymoma found in the conus medullaris or filum terminale region. Intracranial occurrence of the tumor is a rarity. The most characteristic histological feature of myxopapillary tumors is the abundance of intercellular and perivascular mucin and the arborizing vasculature, which tends to form papillae. We are reporting a 14-year-old patient presented with seizures caused by the right occipital region intraparenchymal lesion. Histopathology confirmed it to be MPE. Lesion was excised completely. Literature reviews on the topic are discussed regarding the histological findings, natural history, and outcome of surgically treated MPE. This is the fifth reported case of cerebral intraparenchymal primary MPE. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5652108/ /pubmed/29114296 http://dx.doi.org/10.4103/ajns.AJNS_45_15 Text en Copyright: © 2017 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 Case Report
Mewada, Tushit Bharat
Bishnoi, Ishu Hetram
Singh, Hukum
Singh, Daljit
Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title_full Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title_fullStr Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title_full_unstemmed Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title_short Occipital Intraparenchymal Myxopapillary Ependymoma: Case Report and Literature Review
title_sort occipital intraparenchymal myxopapillary ependymoma: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652108/
https://www.ncbi.nlm.nih.gov/pubmed/29114296
http://dx.doi.org/10.4103/ajns.AJNS_45_15
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