Aggressive NK/T cell leukemia/lymphoma associated with EBV.

Detalhes bibliográficos
Autor(a) principal: Sousa, Jamira
Data de Publicação: 2011
Outros Autores: Cabezuelo, Lourdes, Almeida, Sérgio, Filipe, Carlos, Simão, Adélia, Carvalho, Armando, Nascimento Costa, J
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/1547
Resumo: The authors describe an unusual case of a young man presenting with fever, asthenia, anorexia and jaundice, associated to hepatosplenomegaly, evolving rapidly to multiorganic failure. Final diagnosis revealed an aggressive NK cell leukemia/lymphoma associated to the Epstein-Barr virus (EBV). The diagnosis, suggested clinically and after bone marrow immunophenotyping, was confirmed by morphologic and immunohistochemical findings on the post-mortem hepatic and splenic biopsy .The tumor cells were positive for CD3 and cytotoxic molecules, TIA, granzyme B and perforin. The herein reported case is a rare clinical entity, only recently recognized and with a difficult early diagnosis. We emphasize the necessity to exclude a Natural Killer cell malignancy in cases with identical characteristics.
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spelling Aggressive NK/T cell leukemia/lymphoma associated with EBV.Leucemia/linfoma agressivo de células NK/T.The authors describe an unusual case of a young man presenting with fever, asthenia, anorexia and jaundice, associated to hepatosplenomegaly, evolving rapidly to multiorganic failure. Final diagnosis revealed an aggressive NK cell leukemia/lymphoma associated to the Epstein-Barr virus (EBV). The diagnosis, suggested clinically and after bone marrow immunophenotyping, was confirmed by morphologic and immunohistochemical findings on the post-mortem hepatic and splenic biopsy .The tumor cells were positive for CD3 and cytotoxic molecules, TIA, granzyme B and perforin. The herein reported case is a rare clinical entity, only recently recognized and with a difficult early diagnosis. We emphasize the necessity to exclude a Natural Killer cell malignancy in cases with identical characteristics.The authors describe an unusual case of a young man presenting with fever, asthenia, anorexia and jaundice, associated to hepatosplenomegaly, evolving rapidly to multiorganic failure. Final diagnosis revealed an aggressive NK cell leukemia/lymphoma associated to the Epstein-Barr virus (EBV). The diagnosis, suggested clinically and after bone marrow immunophenotyping, was confirmed by morphologic and immunohistochemical findings on the post-mortem hepatic and splenic biopsy .The tumor cells were positive for CD3 and cytotoxic molecules, TIA, granzyme B and perforin. The herein reported case is a rare clinical entity, only recently recognized and with a difficult early diagnosis. We emphasize the necessity to exclude a Natural Killer cell malignancy in cases with identical characteristics.Ordem dos Médicos2011-12-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1547oai:ojs.www.actamedicaportuguesa.com:article/1547Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 649-52Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 649-521646-07580870-399Xreponame: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/1547https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1547/1132Sousa, JamiraCabezuelo, LourdesAlmeida, SérgioFilipe, CarlosSimão, AdéliaCarvalho, ArmandoNascimento Costa, Jinfo:eu-repo/semantics/openAccess2022-12-20T10:58:06Zoai:ojs.www.actamedicaportuguesa.com:article/1547Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:17:13.528923Repositório 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 Aggressive NK/T cell leukemia/lymphoma associated with EBV.
Leucemia/linfoma agressivo de células NK/T.
title Aggressive NK/T cell leukemia/lymphoma associated with EBV.
spellingShingle Aggressive NK/T cell leukemia/lymphoma associated with EBV.
Sousa, Jamira
title_short Aggressive NK/T cell leukemia/lymphoma associated with EBV.
title_full Aggressive NK/T cell leukemia/lymphoma associated with EBV.
title_fullStr Aggressive NK/T cell leukemia/lymphoma associated with EBV.
title_full_unstemmed Aggressive NK/T cell leukemia/lymphoma associated with EBV.
title_sort Aggressive NK/T cell leukemia/lymphoma associated with EBV.
author Sousa, Jamira
author_facet Sousa, Jamira
Cabezuelo, Lourdes
Almeida, Sérgio
Filipe, Carlos
Simão, Adélia
Carvalho, Armando
Nascimento Costa, J
author_role author
author2 Cabezuelo, Lourdes
Almeida, Sérgio
Filipe, Carlos
Simão, Adélia
Carvalho, Armando
Nascimento Costa, J
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sousa, Jamira
Cabezuelo, Lourdes
Almeida, Sérgio
Filipe, Carlos
Simão, Adélia
Carvalho, Armando
Nascimento Costa, J
description The authors describe an unusual case of a young man presenting with fever, asthenia, anorexia and jaundice, associated to hepatosplenomegaly, evolving rapidly to multiorganic failure. Final diagnosis revealed an aggressive NK cell leukemia/lymphoma associated to the Epstein-Barr virus (EBV). The diagnosis, suggested clinically and after bone marrow immunophenotyping, was confirmed by morphologic and immunohistochemical findings on the post-mortem hepatic and splenic biopsy .The tumor cells were positive for CD3 and cytotoxic molecules, TIA, granzyme B and perforin. The herein reported case is a rare clinical entity, only recently recognized and with a difficult early diagnosis. We emphasize the necessity to exclude a Natural Killer cell malignancy in cases with identical characteristics.
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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url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1547
identifier_str_mv oai:ojs.www.actamedicaportuguesa.com:article/1547
dc.language.iso.fl_str_mv por
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1547/1132
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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; 649-52
Acta Médica Portuguesa; Vol. 24 (2011): Suplemento 3; 649-52
1646-0758
0870-399X
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