Gliosarcomas.
Autor(a) principal: | |
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Data de Publicação: | 1998 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266 |
Resumo: | Gliosarcomas are rare tumors of the central nervous system with a poor prognosis. Histologically these tumors are characterized by an admixture of neoplastic glial cells and sarcomatous elements. Due to the scarcity of data in literature, the diagnosis is often missed and treatment is difficult. The authors report three cases of cerebral gliosarcomas and review the literature on this subject. |
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Gliosarcomas.Gliossarcomas.Gliosarcomas are rare tumors of the central nervous system with a poor prognosis. Histologically these tumors are characterized by an admixture of neoplastic glial cells and sarcomatous elements. Due to the scarcity of data in literature, the diagnosis is often missed and treatment is difficult. The authors report three cases of cerebral gliosarcomas and review the literature on this subject.Gliosarcomas are rare tumors of the central nervous system with a poor prognosis. Histologically these tumors are characterized by an admixture of neoplastic glial cells and sarcomatous elements. Due to the scarcity of data in literature, the diagnosis is often missed and treatment is difficult. The authors report three cases of cerebral gliosarcomas and review the literature on this subject.Ordem dos Médicos1998-06-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266oai:ojs.www.actamedicaportuguesa.com:article/2266Acta Médica Portuguesa; Vol. 11 No. 6 (1998): Junho; 573-6Acta Médica Portuguesa; Vol. 11 N.º 6 (1998): Junho; 573-61646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266/1685Sousa, OHonavar, MFernandes, TVieira, ELopes, Cinfo:eu-repo/semantics/openAccess2022-12-20T11:00:10Zoai:ojs.www.actamedicaportuguesa.com:article/2266Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:17:38.098691Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Gliosarcomas. Gliossarcomas. |
title |
Gliosarcomas. |
spellingShingle |
Gliosarcomas. Sousa, O |
title_short |
Gliosarcomas. |
title_full |
Gliosarcomas. |
title_fullStr |
Gliosarcomas. |
title_full_unstemmed |
Gliosarcomas. |
title_sort |
Gliosarcomas. |
author |
Sousa, O |
author_facet |
Sousa, O Honavar, M Fernandes, T Vieira, E Lopes, C |
author_role |
author |
author2 |
Honavar, M Fernandes, T Vieira, E Lopes, C |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Sousa, O Honavar, M Fernandes, T Vieira, E Lopes, C |
description |
Gliosarcomas are rare tumors of the central nervous system with a poor prognosis. Histologically these tumors are characterized by an admixture of neoplastic glial cells and sarcomatous elements. Due to the scarcity of data in literature, the diagnosis is often missed and treatment is difficult. The authors report three cases of cerebral gliosarcomas and review the literature on this subject. |
publishDate |
1998 |
dc.date.none.fl_str_mv |
1998-06-30 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
format |
article |
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publishedVersion |
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266 oai:ojs.www.actamedicaportuguesa.com:article/2266 |
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266 |
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oai:ojs.www.actamedicaportuguesa.com:article/2266 |
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por |
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por |
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266/1685 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Ordem dos Médicos |
publisher.none.fl_str_mv |
Ordem dos Médicos |
dc.source.none.fl_str_mv |
Acta Médica Portuguesa; Vol. 11 No. 6 (1998): Junho; 573-6 Acta Médica Portuguesa; Vol. 11 N.º 6 (1998): Junho; 573-6 1646-0758 0870-399X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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