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Parieto-temporal pleomorphic xanthoastrocytoma in a black African child

Pleomorphic xanthoastrocytoma (PXA) is a rare cerebral tumor, accounting for <1% of all astrocytic neoplasms. PXA, usually, has a favorable prognosis in spite of what might be suggested from the ominous microscopic appearance. There is no literature immediately available on the black population f...

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Autores principales: Musara, Aaron, Kalangu, Kazadi K., Dzowa, Maximillan N., Muteweye, Wilfred, Mutasa, Rudo
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/PMC5409394/
https://www.ncbi.nlm.nih.gov/pubmed/28484558
http://dx.doi.org/10.4103/1793-5482.145535
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author Musara, Aaron
Kalangu, Kazadi K.
Dzowa, Maximillan N.
Muteweye, Wilfred
Mutasa, Rudo
author_facet Musara, Aaron
Kalangu, Kazadi K.
Dzowa, Maximillan N.
Muteweye, Wilfred
Mutasa, Rudo
author_sort Musara, Aaron
collection PubMed
description Pleomorphic xanthoastrocytoma (PXA) is a rare cerebral tumor, accounting for <1% of all astrocytic neoplasms. PXA, usually, has a favorable prognosis in spite of what might be suggested from the ominous microscopic appearance. There is no literature immediately available on the black population for this tumor. Management is by surgical resection. The ideal is gross total resection, which offers an excellent prognosis. This disease condition has not been reported in the black population. The following is a presentation of a case report in a black African girl, followed by a review of the literature.
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spelling pubmed-54093942017-05-08 Parieto-temporal pleomorphic xanthoastrocytoma in a black African child Musara, Aaron Kalangu, Kazadi K. Dzowa, Maximillan N. Muteweye, Wilfred Mutasa, Rudo Asian J Neurosurg Case Report Pleomorphic xanthoastrocytoma (PXA) is a rare cerebral tumor, accounting for <1% of all astrocytic neoplasms. PXA, usually, has a favorable prognosis in spite of what might be suggested from the ominous microscopic appearance. There is no literature immediately available on the black population for this tumor. Management is by surgical resection. The ideal is gross total resection, which offers an excellent prognosis. This disease condition has not been reported in the black population. The following is a presentation of a case report in a black African girl, followed by a review of the literature. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5409394/ /pubmed/28484558 http://dx.doi.org/10.4103/1793-5482.145535 Text en Copyright: © 2014 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
Musara, Aaron
Kalangu, Kazadi K.
Dzowa, Maximillan N.
Muteweye, Wilfred
Mutasa, Rudo
Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title_full Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title_fullStr Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title_full_unstemmed Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title_short Parieto-temporal pleomorphic xanthoastrocytoma in a black African child
title_sort parieto-temporal pleomorphic xanthoastrocytoma in a black african child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409394/
https://www.ncbi.nlm.nih.gov/pubmed/28484558
http://dx.doi.org/10.4103/1793-5482.145535
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