Churg-Strauss syndrome: a disabling disease.

Detalhes bibliográficos
Autor(a) principal: André, M C
Data de Publicação: 2011
Outros Autores: Fraga, A, Reis, M Duarte, Filipe, P, Soares de Almeida, L M, Marques Gomes, M A
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/497
Resumo: Churg-Strauss syndrome (CSS) is an infrequent vasculitis that affects small to medium-sized vessels. We describe a 51 year-old-female admitted to our inpatient unit with bullae on her right foot and forearm with pain, paresthesias and impotence of the foot. There was rapid clinical deterioration with lost of gait and peripheral eosinophilia. Histopathology showed many extravascular eosinophils. Bone marrow had an increased number of eosinophils and their precursors with no neoplastic cells infiltration. Electromyogram revealed mononeuritis multiplex with bilateral sciatic and right femoral nerve involvement. She fulfilled the eligibility criteria of American College of Rheumatology (ACR) and Chapell Hill Conference Consensus (CHCC) of CSS so corticosteroids and cyclophosphamide and rehabilitation program were begun with good clinical and laboratorial response. This report illustrates the importance of identifying atypical cutaneous features of CSS for the early diagnosis of this rare condition and the role of a multidisciplinary team in this multissystemic disease.
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spelling Churg-Strauss syndrome: a disabling disease.Síndrome de churg-strauss: uma doença incapacitante.Churg-Strauss syndrome (CSS) is an infrequent vasculitis that affects small to medium-sized vessels. We describe a 51 year-old-female admitted to our inpatient unit with bullae on her right foot and forearm with pain, paresthesias and impotence of the foot. There was rapid clinical deterioration with lost of gait and peripheral eosinophilia. Histopathology showed many extravascular eosinophils. Bone marrow had an increased number of eosinophils and their precursors with no neoplastic cells infiltration. Electromyogram revealed mononeuritis multiplex with bilateral sciatic and right femoral nerve involvement. She fulfilled the eligibility criteria of American College of Rheumatology (ACR) and Chapell Hill Conference Consensus (CHCC) of CSS so corticosteroids and cyclophosphamide and rehabilitation program were begun with good clinical and laboratorial response. This report illustrates the importance of identifying atypical cutaneous features of CSS for the early diagnosis of this rare condition and the role of a multidisciplinary team in this multissystemic disease.Churg-Strauss syndrome (CSS) is an infrequent vasculitis that affects small to medium-sized vessels. We describe a 51 year-old-female admitted to our inpatient unit with bullae on her right foot and forearm with pain, paresthesias and impotence of the foot. There was rapid clinical deterioration with lost of gait and peripheral eosinophilia. Histopathology showed many extravascular eosinophils. Bone marrow had an increased number of eosinophils and their precursors with no neoplastic cells infiltration. Electromyogram revealed mononeuritis multiplex with bilateral sciatic and right femoral nerve involvement. She fulfilled the eligibility criteria of American College of Rheumatology (ACR) and Chapell Hill Conference Consensus (CHCC) of CSS so corticosteroids and cyclophosphamide and rehabilitation program were begun with good clinical and laboratorial response. This report illustrates the importance of identifying atypical cutaneous features of CSS for the early diagnosis of this rare condition and the role of a multidisciplinary team in this multissystemic disease.Ordem dos Médicos2011-12-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/497oai:ojs.www.actamedicaportuguesa.com:article/497Acta Médica Portuguesa; Vol. 24 No. 5 (2011): Setembro-Outubro; 853-6Acta Médica Portuguesa; Vol. 24 N.º 5 (2011): Setembro-Outubro; 853-61646-07580870-399Xreponame: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/497https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/497/205André, M CFraga, AReis, M DuarteFilipe, PSoares de Almeida, L MMarques Gomes, M Ainfo:eu-repo/semantics/openAccess2022-12-20T10:56:23Zoai:ojs.www.actamedicaportuguesa.com:article/497Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:32.335945Repositório 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 Churg-Strauss syndrome: a disabling disease.
Síndrome de churg-strauss: uma doença incapacitante.
title Churg-Strauss syndrome: a disabling disease.
spellingShingle Churg-Strauss syndrome: a disabling disease.
André, M C
title_short Churg-Strauss syndrome: a disabling disease.
title_full Churg-Strauss syndrome: a disabling disease.
title_fullStr Churg-Strauss syndrome: a disabling disease.
title_full_unstemmed Churg-Strauss syndrome: a disabling disease.
title_sort Churg-Strauss syndrome: a disabling disease.
author André, M C
author_facet André, M C
Fraga, A
Reis, M Duarte
Filipe, P
Soares de Almeida, L M
Marques Gomes, M A
author_role author
author2 Fraga, A
Reis, M Duarte
Filipe, P
Soares de Almeida, L M
Marques Gomes, M A
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv André, M C
Fraga, A
Reis, M Duarte
Filipe, P
Soares de Almeida, L M
Marques Gomes, M A
description Churg-Strauss syndrome (CSS) is an infrequent vasculitis that affects small to medium-sized vessels. We describe a 51 year-old-female admitted to our inpatient unit with bullae on her right foot and forearm with pain, paresthesias and impotence of the foot. There was rapid clinical deterioration with lost of gait and peripheral eosinophilia. Histopathology showed many extravascular eosinophils. Bone marrow had an increased number of eosinophils and their precursors with no neoplastic cells infiltration. Electromyogram revealed mononeuritis multiplex with bilateral sciatic and right femoral nerve involvement. She fulfilled the eligibility criteria of American College of Rheumatology (ACR) and Chapell Hill Conference Consensus (CHCC) of CSS so corticosteroids and cyclophosphamide and rehabilitation program were begun with good clinical and laboratorial response. This report illustrates the importance of identifying atypical cutaneous features of CSS for the early diagnosis of this rare condition and the role of a multidisciplinary team in this multissystemic disease.
publishDate 2011
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/497/205
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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 No. 5 (2011): Setembro-Outubro; 853-6
Acta Médica Portuguesa; Vol. 24 N.º 5 (2011): Setembro-Outubro; 853-6
1646-0758
0870-399X
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