Gliosarcomas.

Detalhes bibliográficos
Autor(a) principal: Sousa, O
Data de Publicação: 1998
Outros Autores: Honavar, M, Fernandes, T, Vieira, E, Lopes, C
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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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spelling 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:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron: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/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T10:37:53.473151Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
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
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url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266
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dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/2266
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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
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