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Gliosarcome cérébral primitif: à propos de deux cas et revue de la littérature
Gliosarcoma is a very rare brain tumor accounting for 1.8 -8% of all glial tumors. It has been classified by the World Health Organization as a variant of glioblastoma. It is a tumor with double glial and sarcomatous component. Patient’s clinical picture is polymorphic, imaging data are evocative, d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534136/ https://www.ncbi.nlm.nih.gov/pubmed/28904651 http://dx.doi.org/10.11604/pamj.2017.27.14.8977 |
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author | Azami, Mohamed Amine Alami, Iliass El Bourhafour, Imane Belhabib, Salwa Oukabli, Mohamed Albouzidi, Abderrahmane |
author_facet | Azami, Mohamed Amine Alami, Iliass El Bourhafour, Imane Belhabib, Salwa Oukabli, Mohamed Albouzidi, Abderrahmane |
author_sort | Azami, Mohamed Amine |
collection | PubMed |
description | Gliosarcoma is a very rare brain tumor accounting for 1.8 -8% of all glial tumors. It has been classified by the World Health Organization as a variant of glioblastoma. It is a tumor with double glial and sarcomatous component. Patient’s clinical picture is polymorphic, imaging data are evocative, diagnosis is based on histology. Treatment is always surgical. Prognosis is closely linked to the quality of resection. We here report two clinical cases with the aim of assessing the diagnostic, therapeutic and prognostic features of this rare entity. |
format | Online Article Text |
id | pubmed-5534136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-55341362017-09-13 Gliosarcome cérébral primitif: à propos de deux cas et revue de la littérature Azami, Mohamed Amine Alami, Iliass El Bourhafour, Imane Belhabib, Salwa Oukabli, Mohamed Albouzidi, Abderrahmane Pan Afr Med J Case Report Gliosarcoma is a very rare brain tumor accounting for 1.8 -8% of all glial tumors. It has been classified by the World Health Organization as a variant of glioblastoma. It is a tumor with double glial and sarcomatous component. Patient’s clinical picture is polymorphic, imaging data are evocative, diagnosis is based on histology. Treatment is always surgical. Prognosis is closely linked to the quality of resection. We here report two clinical cases with the aim of assessing the diagnostic, therapeutic and prognostic features of this rare entity. The African Field Epidemiology Network 2017-05-08 /pmc/articles/PMC5534136/ /pubmed/28904651 http://dx.doi.org/10.11604/pamj.2017.27.14.8977 Text en © Mohamed Amine Azami et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Azami, Mohamed Amine Alami, Iliass El Bourhafour, Imane Belhabib, Salwa Oukabli, Mohamed Albouzidi, Abderrahmane Gliosarcome cérébral primitif: à propos de deux cas et revue de la littérature |
title | Gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
title_full | Gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
title_fullStr | Gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
title_full_unstemmed | Gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
title_short | Gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
title_sort | gliosarcome cérébral primitif: à propos de
deux cas et revue de la littérature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534136/ https://www.ncbi.nlm.nih.gov/pubmed/28904651 http://dx.doi.org/10.11604/pamj.2017.27.14.8977 |
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