Adult-onset Still disease as the cause of fever of unknown origin.

Detalhes bibliográficos
Autor(a) principal: Diogo, Marco
Data de Publicação: 2010
Outros Autores: Soares, João, Pimentel, Teresa, Ferreira, Adelina
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/706
Resumo: Fever of unknown origin remains a diagnostic challenge with up to 50% of unexplained cases. Adult-onset Still disease typically present high fever, arthralgia, rash, pharyngitis and serositis, lymphadenopathy and hepatosplenomegaly, inflammatory markers and hepatic enzymes elevation and negative immunological study. The authors present a 46-year old man with previous admissions for fever of unknown origin with a 3-week history of fever and systemic symptoms. The study disclosed anaemia, inflammatory markers and hepatic enzymes elevation, splenomegaly and negative serological and immunological studies. The patient posteriorly presented polyarthralgias and cutaneous rash. The introduction of corticotherapy resolved symptoms and laboratories alterations. Adult-onset Still disease is a heterogeneous and rare disease and the lack of serologic markers as a true gold standard makes diagnosis difficult.
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spelling Adult-onset Still disease as the cause of fever of unknown origin.Doença de still do adulto como causa de síndrome febril indeterminado.Fever of unknown origin remains a diagnostic challenge with up to 50% of unexplained cases. Adult-onset Still disease typically present high fever, arthralgia, rash, pharyngitis and serositis, lymphadenopathy and hepatosplenomegaly, inflammatory markers and hepatic enzymes elevation and negative immunological study. The authors present a 46-year old man with previous admissions for fever of unknown origin with a 3-week history of fever and systemic symptoms. The study disclosed anaemia, inflammatory markers and hepatic enzymes elevation, splenomegaly and negative serological and immunological studies. The patient posteriorly presented polyarthralgias and cutaneous rash. The introduction of corticotherapy resolved symptoms and laboratories alterations. Adult-onset Still disease is a heterogeneous and rare disease and the lack of serologic markers as a true gold standard makes diagnosis difficult.Fever of unknown origin remains a diagnostic challenge with up to 50% of unexplained cases. Adult-onset Still disease typically present high fever, arthralgia, rash, pharyngitis and serositis, lymphadenopathy and hepatosplenomegaly, inflammatory markers and hepatic enzymes elevation and negative immunological study. The authors present a 46-year old man with previous admissions for fever of unknown origin with a 3-week history of fever and systemic symptoms. The study disclosed anaemia, inflammatory markers and hepatic enzymes elevation, splenomegaly and negative serological and immunological studies. The patient posteriorly presented polyarthralgias and cutaneous rash. The introduction of corticotherapy resolved symptoms and laboratories alterations. Adult-onset Still disease is a heterogeneous and rare disease and the lack of serologic markers as a true gold standard makes diagnosis difficult.Ordem dos Médicos2010-10-22info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/706oai:ojs.www.actamedicaportuguesa.com:article/706Acta Médica Portuguesa; Vol. 23 No. 5 (2010): September-October; 927-30Acta Médica Portuguesa; Vol. 23 N.º 5 (2010): Setembro-Outubro; 927-301646-07580870-399Xreponame: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/706https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/706/384Diogo, MarcoSoares, JoãoPimentel, TeresaFerreira, Adelinainfo:eu-repo/semantics/openAccess2022-12-20T10:56:45Zoai:ojs.www.actamedicaportuguesa.com:article/706Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:42.085428Repositório 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 Adult-onset Still disease as the cause of fever of unknown origin.
Doença de still do adulto como causa de síndrome febril indeterminado.
title Adult-onset Still disease as the cause of fever of unknown origin.
spellingShingle Adult-onset Still disease as the cause of fever of unknown origin.
Diogo, Marco
title_short Adult-onset Still disease as the cause of fever of unknown origin.
title_full Adult-onset Still disease as the cause of fever of unknown origin.
title_fullStr Adult-onset Still disease as the cause of fever of unknown origin.
title_full_unstemmed Adult-onset Still disease as the cause of fever of unknown origin.
title_sort Adult-onset Still disease as the cause of fever of unknown origin.
author Diogo, Marco
author_facet Diogo, Marco
Soares, João
Pimentel, Teresa
Ferreira, Adelina
author_role author
author2 Soares, João
Pimentel, Teresa
Ferreira, Adelina
author2_role author
author
author
dc.contributor.author.fl_str_mv Diogo, Marco
Soares, João
Pimentel, Teresa
Ferreira, Adelina
description Fever of unknown origin remains a diagnostic challenge with up to 50% of unexplained cases. Adult-onset Still disease typically present high fever, arthralgia, rash, pharyngitis and serositis, lymphadenopathy and hepatosplenomegaly, inflammatory markers and hepatic enzymes elevation and negative immunological study. The authors present a 46-year old man with previous admissions for fever of unknown origin with a 3-week history of fever and systemic symptoms. The study disclosed anaemia, inflammatory markers and hepatic enzymes elevation, splenomegaly and negative serological and immunological studies. The patient posteriorly presented polyarthralgias and cutaneous rash. The introduction of corticotherapy resolved symptoms and laboratories alterations. Adult-onset Still disease is a heterogeneous and rare disease and the lack of serologic markers as a true gold standard makes diagnosis difficult.
publishDate 2010
dc.date.none.fl_str_mv 2010-10-22
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/706
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url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/706
identifier_str_mv oai:ojs.www.actamedicaportuguesa.com:article/706
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/706
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/706/384
dc.rights.driver.fl_str_mv info:eu-repo/semantics/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. 23 No. 5 (2010): September-October; 927-30
Acta Médica Portuguesa; Vol. 23 N.º 5 (2010): Setembro-Outubro; 927-30
1646-0758
0870-399X
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