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Pure cortical ependymoma: A rare entity
Ependymomas are mostly infratentorial, intraventricular tumor, accounting for 2–9% of all central nervous system tumors. Supratentorial pure cortical ependymoma are extremely rare tumor with definite ependymal morphology and uncertain histogenesis. They are mostly low grade tumor and are cured with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421963/ https://www.ncbi.nlm.nih.gov/pubmed/25972957 http://dx.doi.org/10.4103/1793-5482.152111 |
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author | Bijwe, Sanjay Ansari, Sameer Jadhav, Vinod Palande, Deepak |
author_facet | Bijwe, Sanjay Ansari, Sameer Jadhav, Vinod Palande, Deepak |
author_sort | Bijwe, Sanjay |
collection | PubMed |
description | Ependymomas are mostly infratentorial, intraventricular tumor, accounting for 2–9% of all central nervous system tumors. Supratentorial pure cortical ependymoma are extremely rare tumor with definite ependymal morphology and uncertain histogenesis. They are mostly low grade tumor and are cured with resection, rendering them favorable prognosis. Our case is of 14-year-old female presenting with headache and convulsion of short duration. She underwent gross total excision of the tumor without radiation therapy and her follow-up is uneventful. |
format | Online Article Text |
id | pubmed-4421963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44219632015-05-13 Pure cortical ependymoma: A rare entity Bijwe, Sanjay Ansari, Sameer Jadhav, Vinod Palande, Deepak Asian J Neurosurg Case Report Ependymomas are mostly infratentorial, intraventricular tumor, accounting for 2–9% of all central nervous system tumors. Supratentorial pure cortical ependymoma are extremely rare tumor with definite ependymal morphology and uncertain histogenesis. They are mostly low grade tumor and are cured with resection, rendering them favorable prognosis. Our case is of 14-year-old female presenting with headache and convulsion of short duration. She underwent gross total excision of the tumor without radiation therapy and her follow-up is uneventful. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4421963/ /pubmed/25972957 http://dx.doi.org/10.4103/1793-5482.152111 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bijwe, Sanjay Ansari, Sameer Jadhav, Vinod Palande, Deepak Pure cortical ependymoma: A rare entity |
title | Pure cortical ependymoma: A rare entity |
title_full | Pure cortical ependymoma: A rare entity |
title_fullStr | Pure cortical ependymoma: A rare entity |
title_full_unstemmed | Pure cortical ependymoma: A rare entity |
title_short | Pure cortical ependymoma: A rare entity |
title_sort | pure cortical ependymoma: a rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421963/ https://www.ncbi.nlm.nih.gov/pubmed/25972957 http://dx.doi.org/10.4103/1793-5482.152111 |
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