Vasculites pulmonares: novas visões de uma velha conhecida

Detalhes bibliográficos
Autor(a) principal: Queluz, Thais Thomaz [UNESP]
Data de Publicação: 2005
Outros Autores: Yoo, Hugo Hyung Bok [UNESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S1806-37132005000700003
http://hdl.handle.net/11449/213118
Resumo: Necrotizing vasculitis was first described in 1866. The condition encompasses a wide spectrum of symptoms, affecting arterial blood vessels of various calibers and in various organs. In addition, it is associated with many types of inflammatory infiltrate, and presents a significant number of clinical manifestations. The causative factor or factors may or may not be identifiable. The eternally controversial classification of the various forms of vasculitis changed radically after the discovery of antineutrophil cytoplasmic antibodies in 1982, and current classifications include Goodpasture's syndrome, forms of vasculitis related to antineutrophil cytoplasmic antibodies, forms caused by immune complexes and other forms. The evidence that antineutrophil cytoplasmic antibodies are involved in the pathogenesis of such conditions led to considerable advances in the diagnosis and treatment of vasculitis. Wegener's granulomatosis, Churg-Strauss syndrome and microscopic polyangiitis, all forms of vasculitis that have been associated with antineutrophil cytoplasmic antibodies, are the systemic forms that most affect the lungs. The most common presentation of such forms is characterized by cough, diffuse alveolar hemorrhage or difficult-to-control asthma. In Takayasu's arteritis, Behçet's disease and Henoch-Schönlein purpura, as well as in forms of vasculitis related to collagen diseases, pulmonary involvement is less common. In all forms of vasculitis, there is evidence that immune system processes are involved. It is based on this knowledge that new therapeutic approaches are proposed.
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spelling Vasculites pulmonares: novas visões de uma velha conhecidaPulmonary forms of vasculitis: new perspectives on an old acquaintanceVasculitisAntibodies, antineutrophil cytoplasmicWegener's granulomatosisVasculitesAnticorpos anticitoplasma de neutrófilosGranulomatose de WegenerNecrotizing vasculitis was first described in 1866. The condition encompasses a wide spectrum of symptoms, affecting arterial blood vessels of various calibers and in various organs. In addition, it is associated with many types of inflammatory infiltrate, and presents a significant number of clinical manifestations. The causative factor or factors may or may not be identifiable. The eternally controversial classification of the various forms of vasculitis changed radically after the discovery of antineutrophil cytoplasmic antibodies in 1982, and current classifications include Goodpasture's syndrome, forms of vasculitis related to antineutrophil cytoplasmic antibodies, forms caused by immune complexes and other forms. The evidence that antineutrophil cytoplasmic antibodies are involved in the pathogenesis of such conditions led to considerable advances in the diagnosis and treatment of vasculitis. Wegener's granulomatosis, Churg-Strauss syndrome and microscopic polyangiitis, all forms of vasculitis that have been associated with antineutrophil cytoplasmic antibodies, are the systemic forms that most affect the lungs. The most common presentation of such forms is characterized by cough, diffuse alveolar hemorrhage or difficult-to-control asthma. In Takayasu's arteritis, Behçet's disease and Henoch-Schönlein purpura, as well as in forms of vasculitis related to collagen diseases, pulmonary involvement is less common. In all forms of vasculitis, there is evidence that immune system processes are involved. It is based on this knowledge that new therapeutic approaches are proposed.A vasculite necrosante foi descrita em 1866 e seu espectro é muito amplo, uma vez que acomete vasos arteriais e venosos de todos os calibres e de vários órgãos, apresenta diversos tipos de infiltrados inflamatórios, tem um significante número de manifestações clínicas e pode ter ou não fatores desencadeantes identificáveis. A sempre controversa classificação das vasculites mudou radicalmente com a descoberta dos anticorpos anticitoplasma de neutrófilos em 1982, contemplando atualmente a doença de Goodpasture, as vasculites associadas aos anticorpos anticitoplasma de neutrófilos, as vasculites por imunocomplexos e outros tipos de vasculites. As evidências de que os anticorpos anticitoplasma de neutrófilos estão envolvidos na patogênese destas lesões trouxeram avanços consideráveis para o seu diagnóstico e tratamento. Granulomatose de Wegener, doença de Churg-Strauss e poliangeíte microscópica, todas vasculites associadas aos anticorpos anticitoplasma de neutrófilos, são as vasculites sistêmicas que mais acometem os pulmões. Suas manifestações clínicas comuns são tosse, hemorragia alveolar difusa ou asma de difícil controle. Na arterite de Takayasu, na doença de Behçet, na púrpura de Henoch-Schönlein e nas vasculites associadas às doenças do colágeno o acometimento pulmonar é mais raro. Em todos os casos há evidências de serem processos de origem imunológica e com base neste princípio são propostas as abordagens terapêuticas.Universidade Estadual PaulistaUniversidade Estadual PaulistaSociedade Brasileira de Pneumologia e TisiologiaUniversidade Estadual Paulista (Unesp)Queluz, Thais Thomaz [UNESP]Yoo, Hugo Hyung Bok [UNESP]2021-07-14T10:50:18Z2021-07-14T10:50:18Z2005-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articles1-s3application/pdfhttp://dx.doi.org/10.1590/S1806-37132005000700003Jornal Brasileiro de Pneumologia. São Paulo, SP, Brazil: Sociedade Brasileira de Pneumologia e Tisiologia, v. 31, n. suppl 1, p. s1-s3, 2005.1806-3756http://hdl.handle.net/11449/21311810.1590/S1806-37132005000700003S1806-37132005000700003S1806-37132005000700003.pdfSciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporJornal Brasileiro de Pneumologiainfo:eu-repo/semantics/openAccess2023-11-08T06:13:38Zoai:repositorio.unesp.br:11449/213118Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-08T06:13:38Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Vasculites pulmonares: novas visões de uma velha conhecida
Pulmonary forms of vasculitis: new perspectives on an old acquaintance
title Vasculites pulmonares: novas visões de uma velha conhecida
spellingShingle Vasculites pulmonares: novas visões de uma velha conhecida
Queluz, Thais Thomaz [UNESP]
Vasculitis
Antibodies, antineutrophil cytoplasmic
Wegener's granulomatosis
Vasculites
Anticorpos anticitoplasma de neutrófilos
Granulomatose de Wegener
title_short Vasculites pulmonares: novas visões de uma velha conhecida
title_full Vasculites pulmonares: novas visões de uma velha conhecida
title_fullStr Vasculites pulmonares: novas visões de uma velha conhecida
title_full_unstemmed Vasculites pulmonares: novas visões de uma velha conhecida
title_sort Vasculites pulmonares: novas visões de uma velha conhecida
author Queluz, Thais Thomaz [UNESP]
author_facet Queluz, Thais Thomaz [UNESP]
Yoo, Hugo Hyung Bok [UNESP]
author_role author
author2 Yoo, Hugo Hyung Bok [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Queluz, Thais Thomaz [UNESP]
Yoo, Hugo Hyung Bok [UNESP]
dc.subject.por.fl_str_mv Vasculitis
Antibodies, antineutrophil cytoplasmic
Wegener's granulomatosis
Vasculites
Anticorpos anticitoplasma de neutrófilos
Granulomatose de Wegener
topic Vasculitis
Antibodies, antineutrophil cytoplasmic
Wegener's granulomatosis
Vasculites
Anticorpos anticitoplasma de neutrófilos
Granulomatose de Wegener
description Necrotizing vasculitis was first described in 1866. The condition encompasses a wide spectrum of symptoms, affecting arterial blood vessels of various calibers and in various organs. In addition, it is associated with many types of inflammatory infiltrate, and presents a significant number of clinical manifestations. The causative factor or factors may or may not be identifiable. The eternally controversial classification of the various forms of vasculitis changed radically after the discovery of antineutrophil cytoplasmic antibodies in 1982, and current classifications include Goodpasture's syndrome, forms of vasculitis related to antineutrophil cytoplasmic antibodies, forms caused by immune complexes and other forms. The evidence that antineutrophil cytoplasmic antibodies are involved in the pathogenesis of such conditions led to considerable advances in the diagnosis and treatment of vasculitis. Wegener's granulomatosis, Churg-Strauss syndrome and microscopic polyangiitis, all forms of vasculitis that have been associated with antineutrophil cytoplasmic antibodies, are the systemic forms that most affect the lungs. The most common presentation of such forms is characterized by cough, diffuse alveolar hemorrhage or difficult-to-control asthma. In Takayasu's arteritis, Behçet's disease and Henoch-Schönlein purpura, as well as in forms of vasculitis related to collagen diseases, pulmonary involvement is less common. In all forms of vasculitis, there is evidence that immune system processes are involved. It is based on this knowledge that new therapeutic approaches are proposed.
publishDate 2005
dc.date.none.fl_str_mv 2005-07
2021-07-14T10:50:18Z
2021-07-14T10:50:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S1806-37132005000700003
Jornal Brasileiro de Pneumologia. São Paulo, SP, Brazil: Sociedade Brasileira de Pneumologia e Tisiologia, v. 31, n. suppl 1, p. s1-s3, 2005.
1806-3756
http://hdl.handle.net/11449/213118
10.1590/S1806-37132005000700003
S1806-37132005000700003
S1806-37132005000700003.pdf
url http://dx.doi.org/10.1590/S1806-37132005000700003
http://hdl.handle.net/11449/213118
identifier_str_mv Jornal Brasileiro de Pneumologia. São Paulo, SP, Brazil: Sociedade Brasileira de Pneumologia e Tisiologia, v. 31, n. suppl 1, p. s1-s3, 2005.
1806-3756
10.1590/S1806-37132005000700003
S1806-37132005000700003
S1806-37132005000700003.pdf
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Jornal Brasileiro de Pneumologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv s1-s3
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Pneumologia e Tisiologia
publisher.none.fl_str_mv Sociedade Brasileira de Pneumologia e Tisiologia
dc.source.none.fl_str_mv SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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