Carcinoma pancreático de células gigantes de tipo osteoclástico

Detalhes bibliográficos
Autor(a) principal: Pimentel, A
Data de Publicação: 2010
Outros Autores: Leitão, S, Dias, N, Cipriano, MA, Leite, J, Santos, R, Nascimento-Costa, JM
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.4/897
Resumo: Initially described 40 years ago (Rosai), the undifferentiated osteoclastic-type giant cell carcinoma (IOGCC) is a variant of ductal adenocarcinoma and accounts for less than 1% of exocrine pancreatic tumors. Its extreme rarity, with consequent existence of few reports and clinical experience, leads to the arousal of doubts with regard to its histogenesis, types of approach and therapeutical attitudes. It is important to note that in Portugal no similar case is registered in medical literature. A 61 year old patient admitted to the Internal Medicine Ward 3 at Coimbra University Hospital presents with a volumous intra-abdominal mass in the left hypochondrium and microcytic anemia. During the investigation, a pancreatic neoplasm was identified, and the patient was submitted to surgical resection, the anatomo-pathological study of the tumor having revealed IOGCC. The particularities of the case, current available therapeutical options and its evolution are discussed, as well as a revision of the existing literature.
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spelling Carcinoma pancreático de células gigantes de tipo osteoclásticoIndifferentiated osteoclastic-type giant cell carcinomaNeoplasias do PâncreasOsteoclastosTumores de Células GigantesInitially described 40 years ago (Rosai), the undifferentiated osteoclastic-type giant cell carcinoma (IOGCC) is a variant of ductal adenocarcinoma and accounts for less than 1% of exocrine pancreatic tumors. Its extreme rarity, with consequent existence of few reports and clinical experience, leads to the arousal of doubts with regard to its histogenesis, types of approach and therapeutical attitudes. It is important to note that in Portugal no similar case is registered in medical literature. A 61 year old patient admitted to the Internal Medicine Ward 3 at Coimbra University Hospital presents with a volumous intra-abdominal mass in the left hypochondrium and microcytic anemia. During the investigation, a pancreatic neoplasm was identified, and the patient was submitted to surgical resection, the anatomo-pathological study of the tumor having revealed IOGCC. The particularities of the case, current available therapeutical options and its evolution are discussed, as well as a revision of the existing literature.CELOMRIHUCPimentel, ALeitão, SDias, NCipriano, MALeite, JSantos, RNascimento-Costa, JM2010-12-20T14:48:30Z20102010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.4/897porActa Med Port. 2010 Sep-Oct;23(5):931-936.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-11T14:22:05Zoai:rihuc.huc.min-saude.pt:10400.4/897Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:03:26.040657Repositório 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 Carcinoma pancreático de células gigantes de tipo osteoclástico
Indifferentiated osteoclastic-type giant cell carcinoma
title Carcinoma pancreático de células gigantes de tipo osteoclástico
spellingShingle Carcinoma pancreático de células gigantes de tipo osteoclástico
Pimentel, A
Neoplasias do Pâncreas
Osteoclastos
Tumores de Células Gigantes
title_short Carcinoma pancreático de células gigantes de tipo osteoclástico
title_full Carcinoma pancreático de células gigantes de tipo osteoclástico
title_fullStr Carcinoma pancreático de células gigantes de tipo osteoclástico
title_full_unstemmed Carcinoma pancreático de células gigantes de tipo osteoclástico
title_sort Carcinoma pancreático de células gigantes de tipo osteoclástico
author Pimentel, A
author_facet Pimentel, A
Leitão, S
Dias, N
Cipriano, MA
Leite, J
Santos, R
Nascimento-Costa, JM
author_role author
author2 Leitão, S
Dias, N
Cipriano, MA
Leite, J
Santos, R
Nascimento-Costa, JM
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv RIHUC
dc.contributor.author.fl_str_mv Pimentel, A
Leitão, S
Dias, N
Cipriano, MA
Leite, J
Santos, R
Nascimento-Costa, JM
dc.subject.por.fl_str_mv Neoplasias do Pâncreas
Osteoclastos
Tumores de Células Gigantes
topic Neoplasias do Pâncreas
Osteoclastos
Tumores de Células Gigantes
description Initially described 40 years ago (Rosai), the undifferentiated osteoclastic-type giant cell carcinoma (IOGCC) is a variant of ductal adenocarcinoma and accounts for less than 1% of exocrine pancreatic tumors. Its extreme rarity, with consequent existence of few reports and clinical experience, leads to the arousal of doubts with regard to its histogenesis, types of approach and therapeutical attitudes. It is important to note that in Portugal no similar case is registered in medical literature. A 61 year old patient admitted to the Internal Medicine Ward 3 at Coimbra University Hospital presents with a volumous intra-abdominal mass in the left hypochondrium and microcytic anemia. During the investigation, a pancreatic neoplasm was identified, and the patient was submitted to surgical resection, the anatomo-pathological study of the tumor having revealed IOGCC. The particularities of the case, current available therapeutical options and its evolution are discussed, as well as a revision of the existing literature.
publishDate 2010
dc.date.none.fl_str_mv 2010-12-20T14:48:30Z
2010
2010-01-01T00:00:00Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.4/897
url http://hdl.handle.net/10400.4/897
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv Acta Med Port. 2010 Sep-Oct;23(5):931-936.
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publisher.none.fl_str_mv CELOM
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