Pulmonary hamartoma.
Autor(a) principal: | |
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Data de Publicação: | 2002 |
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/1932 |
Resumo: | The so-called pulmonary hamartomas occur in 0.3% of the general population, with a higher frequency in male gender and in the sixth decade of life. Usually they are single lesions peripherally located in the lung, are formed by mature lobular cartilage and less frequently show adipous and fibromixoid tissue, also with calcified foci. These tumors should be called benign mesenchymomas, due to studies that showed cromossomic alterations and genetic translocations, whose malignant potential has not been recognized. |
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Pulmonary hamartoma.Hamartomas pulmonares.The so-called pulmonary hamartomas occur in 0.3% of the general population, with a higher frequency in male gender and in the sixth decade of life. Usually they are single lesions peripherally located in the lung, are formed by mature lobular cartilage and less frequently show adipous and fibromixoid tissue, also with calcified foci. These tumors should be called benign mesenchymomas, due to studies that showed cromossomic alterations and genetic translocations, whose malignant potential has not been recognized.The so-called pulmonary hamartomas occur in 0.3% of the general population, with a higher frequency in male gender and in the sixth decade of life. Usually they are single lesions peripherally located in the lung, are formed by mature lobular cartilage and less frequently show adipous and fibromixoid tissue, also with calcified foci. These tumors should be called benign mesenchymomas, due to studies that showed cromossomic alterations and genetic translocations, whose malignant potential has not been recognized.Ordem dos Médicos2002-06-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932oai:ojs.www.actamedicaportuguesa.com:article/1932Acta Médica Portuguesa; Vol. 15 No. 3 (2002): Maio-Junho; 165-8Acta Médica Portuguesa; Vol. 15 N.º 3 (2002): Maio-Junho; 165-81646-07580870-399Xreponame: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/1932https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932/1500Matos, RitaCarvalho, Linainfo:eu-repo/semantics/openAccess2022-12-20T10:59:34Zoai:ojs.www.actamedicaportuguesa.com:article/1932Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:17:29.582041Repositório 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 |
Pulmonary hamartoma. Hamartomas pulmonares. |
title |
Pulmonary hamartoma. |
spellingShingle |
Pulmonary hamartoma. Matos, Rita |
title_short |
Pulmonary hamartoma. |
title_full |
Pulmonary hamartoma. |
title_fullStr |
Pulmonary hamartoma. |
title_full_unstemmed |
Pulmonary hamartoma. |
title_sort |
Pulmonary hamartoma. |
author |
Matos, Rita |
author_facet |
Matos, Rita Carvalho, Lina |
author_role |
author |
author2 |
Carvalho, Lina |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Matos, Rita Carvalho, Lina |
description |
The so-called pulmonary hamartomas occur in 0.3% of the general population, with a higher frequency in male gender and in the sixth decade of life. Usually they are single lesions peripherally located in the lung, are formed by mature lobular cartilage and less frequently show adipous and fibromixoid tissue, also with calcified foci. These tumors should be called benign mesenchymomas, due to studies that showed cromossomic alterations and genetic translocations, whose malignant potential has not been recognized. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002-06-30 |
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info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932 oai:ojs.www.actamedicaportuguesa.com:article/1932 |
url |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932 |
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oai:ojs.www.actamedicaportuguesa.com:article/1932 |
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por |
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por |
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1932/1500 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Ordem dos Médicos |
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Ordem dos Médicos |
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Acta Médica Portuguesa; Vol. 15 No. 3 (2002): Maio-Junho; 165-8 Acta Médica Portuguesa; Vol. 15 N.º 3 (2002): Maio-Junho; 165-8 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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