Langerhans cell histiocytosis and breast.

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Cátia
Data de Publicação: 2011
Outros Autores: Santos, Paulo, Simões, Dora, Valério, Maria Odete, Calhaz-Jorge, C
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/1533
Resumo: Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass. She underwent excisional biopsy. Immunohistochemical and pathological evaluation revealed Langerhans cell histiocytosis. No multisystem involvement was found.
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spelling Langerhans cell histiocytosis and breast.Doença de células de langerhans e mama.Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass. She underwent excisional biopsy. Immunohistochemical and pathological evaluation revealed Langerhans cell histiocytosis. No multisystem involvement was found.Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass. She underwent excisional biopsy. Immunohistochemical and pathological evaluation revealed Langerhans cell histiocytosis. No multisystem involvement was found.Ordem dos Médicos2011-12-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1533oai:ojs.www.actamedicaportuguesa.com:article/1533Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 713-4Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 713-41646-07580870-399Xreponame: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/1533https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1533/1118Rodrigues, CátiaSantos, PauloSimões, DoraValério, Maria OdeteCalhaz-Jorge, Cinfo:eu-repo/semantics/openAccess2022-12-20T10:58:03Zoai:ojs.www.actamedicaportuguesa.com:article/1533Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:17:12.857983Repositório 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 Langerhans cell histiocytosis and breast.
Doença de células de langerhans e mama.
title Langerhans cell histiocytosis and breast.
spellingShingle Langerhans cell histiocytosis and breast.
Rodrigues, Cátia
title_short Langerhans cell histiocytosis and breast.
title_full Langerhans cell histiocytosis and breast.
title_fullStr Langerhans cell histiocytosis and breast.
title_full_unstemmed Langerhans cell histiocytosis and breast.
title_sort Langerhans cell histiocytosis and breast.
author Rodrigues, Cátia
author_facet Rodrigues, Cátia
Santos, Paulo
Simões, Dora
Valério, Maria Odete
Calhaz-Jorge, C
author_role author
author2 Santos, Paulo
Simões, Dora
Valério, Maria Odete
Calhaz-Jorge, C
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Cátia
Santos, Paulo
Simões, Dora
Valério, Maria Odete
Calhaz-Jorge, C
description Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass. She underwent excisional biopsy. Immunohistochemical and pathological evaluation revealed Langerhans cell histiocytosis. No multisystem involvement was found.
publishDate 2011
dc.date.none.fl_str_mv 2011-12-30
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dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1533
oai:ojs.www.actamedicaportuguesa.com:article/1533
url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1533
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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/1533
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1533/1118
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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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. 24 (2011): Suplemento 3; 713-4
Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 713-4
1646-0758
0870-399X
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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