Granulomatosis with polyangiitis: case report with oral involvement

Detalhes bibliográficos
Autor(a) principal: Barroso Generoso, Alana
Data de Publicação: 2020
Outros Autores: Pereira Júnior, Antônio José Araújo, Gontijo Quadros Ferreira, Carolina, Bauti Pinto, Isabela, Viana Milagres, Marcos Paulo
Tipo de documento: Artigo
Idioma: por
Título da fonte: HU Revista (Online)
Texto Completo: https://periodicos.ufjf.br/index.php/hurevista/article/view/30171
Resumo: Introduction: Granulomatosis with polyangiitis (GPA) is described as a triad of lesions, consisting of necrotizing granuloma of the respiratory tract, small and medium-sized disseminated vasculitis and glomerulonephritis. It represents the most frequent of systemic vasculitis.Objective:Currently, there is a shortage of data related to the profile of these patients in the country, with their clinical and epidemiological manifestations. Thus, the case presented aims to contribute to possible other patients who are in the same situation through knowledge of this clinical manifestation and an attempt to approach the complications associated with the disease described.Case report:This report describes the oral involvement with the formation of a deep ulceration, leading to communication between the oral and nasal cavities. Conclusion:Given the above, we reinforce the importance of an early diagnosis, made by an interdisciplinary team, in order to institute appropriate therapy and provide the patient with a longer survival.
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spelling Granulomatosis with polyangiitis: case report with oral involvementGranulomatose com poliangiite: relato de caso com acometimento oralGranulomatosis with PolyangiitisVasculitisWegener`s granulomatosis;Anti-neutrophil cytoplasmic antibodyGranulomatose com PoliangiiteVasculiteGranulomatose de WegenerAnticorpo anticitoplasma de neutrófilosIntroduction: Granulomatosis with polyangiitis (GPA) is described as a triad of lesions, consisting of necrotizing granuloma of the respiratory tract, small and medium-sized disseminated vasculitis and glomerulonephritis. It represents the most frequent of systemic vasculitis.Objective:Currently, there is a shortage of data related to the profile of these patients in the country, with their clinical and epidemiological manifestations. Thus, the case presented aims to contribute to possible other patients who are in the same situation through knowledge of this clinical manifestation and an attempt to approach the complications associated with the disease described.Case report:This report describes the oral involvement with the formation of a deep ulceration, leading to communication between the oral and nasal cavities. Conclusion:Given the above, we reinforce the importance of an early diagnosis, made by an interdisciplinary team, in order to institute appropriate therapy and provide the patient with a longer survival.Introdução: A granulomatose com poliangiite (GPA) é descrita como uma tríade de lesões, constituídas por granuloma necrosante do trato respiratório, vasculite disseminada de pequeno e médio calibre e glomerulonefrite. Representa a mais frequente das vasculites sistêmicas. Objetivo: Atualmente há uma escassez de dados relacionados ao perfil destes pacientes no país, com suas manifestações clínicas e epidemiológicas. Dessa forma, o caso apresentado visa contribuir com possíveis outros pacientes que se encontram na mesma situação por meio do conhecimento desta manifestação clínica e tentativa de abordagem terapêutica de complicações associadas à doença descrita. Relato de caso: O presente relato descreve o acometimento oral com formação de uma ulceração profunda, levando à comunicação entre a cavidade oral e a nasal. Conclusão: Diante do exposto, reforçamos a importância de um diagnóstico precoce, feito por uma equipe interdisciplinar, a fim de instituir a terapêutica adequada e proporcionar ao paciente uma maior sobrevida.  Editora UFJF2020-08-31info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelCasapplication/pdfhttps://periodicos.ufjf.br/index.php/hurevista/article/view/3017110.34019/1982-8047.2020.v46.30171HU Revista; v. 46 (2020); 1-61982-80470103-3123reponame:HU Revista (Online)instname:Universidade Federal de Juiz de Fora (UFJF)instacron:UFJFporhttps://periodicos.ufjf.br/index.php/hurevista/article/view/30171/21077Copyright (c) 2020 Alana Barroso Generoso, Antônio José Araújo Pereira Júnior, Carolina Gontijo Quadros Ferreira, Isabela Bauti Pinto, Marcos Paulo Viana Milagresinfo:eu-repo/semantics/openAccessBarroso Generoso, Alana Pereira Júnior, Antônio José AraújoGontijo Quadros Ferreira, Carolina Bauti Pinto, Isabela Viana Milagres, Marcos Paulo 2020-11-20T19:39:06Zoai:periodicos.ufjf.br:article/30171Revistahttps://periodicos.ufjf.br/index.php/hurevistaPUBhttps://periodicos.ufjf.br/index.php/hurevista/oairevista.hurevista@ufjf.edu.br1982-80470103-3123opendoar:2020-11-20T19:39:06HU Revista (Online) - Universidade Federal de Juiz de Fora (UFJF)false
dc.title.none.fl_str_mv Granulomatosis with polyangiitis: case report with oral involvement
Granulomatose com poliangiite: relato de caso com acometimento oral
title Granulomatosis with polyangiitis: case report with oral involvement
spellingShingle Granulomatosis with polyangiitis: case report with oral involvement
Barroso Generoso, Alana
Granulomatosis with Polyangiitis
Vasculitis
Wegener`s granulomatosis;
Anti-neutrophil cytoplasmic antibody
Granulomatose com Poliangiite
Vasculite
Granulomatose de Wegener
Anticorpo anticitoplasma de neutrófilos
title_short Granulomatosis with polyangiitis: case report with oral involvement
title_full Granulomatosis with polyangiitis: case report with oral involvement
title_fullStr Granulomatosis with polyangiitis: case report with oral involvement
title_full_unstemmed Granulomatosis with polyangiitis: case report with oral involvement
title_sort Granulomatosis with polyangiitis: case report with oral involvement
author Barroso Generoso, Alana
author_facet Barroso Generoso, Alana
Pereira Júnior, Antônio José Araújo
Gontijo Quadros Ferreira, Carolina
Bauti Pinto, Isabela
Viana Milagres, Marcos Paulo
author_role author
author2 Pereira Júnior, Antônio José Araújo
Gontijo Quadros Ferreira, Carolina
Bauti Pinto, Isabela
Viana Milagres, Marcos Paulo
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Barroso Generoso, Alana
Pereira Júnior, Antônio José Araújo
Gontijo Quadros Ferreira, Carolina
Bauti Pinto, Isabela
Viana Milagres, Marcos Paulo
dc.subject.por.fl_str_mv Granulomatosis with Polyangiitis
Vasculitis
Wegener`s granulomatosis;
Anti-neutrophil cytoplasmic antibody
Granulomatose com Poliangiite
Vasculite
Granulomatose de Wegener
Anticorpo anticitoplasma de neutrófilos
topic Granulomatosis with Polyangiitis
Vasculitis
Wegener`s granulomatosis;
Anti-neutrophil cytoplasmic antibody
Granulomatose com Poliangiite
Vasculite
Granulomatose de Wegener
Anticorpo anticitoplasma de neutrófilos
description Introduction: Granulomatosis with polyangiitis (GPA) is described as a triad of lesions, consisting of necrotizing granuloma of the respiratory tract, small and medium-sized disseminated vasculitis and glomerulonephritis. It represents the most frequent of systemic vasculitis.Objective:Currently, there is a shortage of data related to the profile of these patients in the country, with their clinical and epidemiological manifestations. Thus, the case presented aims to contribute to possible other patients who are in the same situation through knowledge of this clinical manifestation and an attempt to approach the complications associated with the disease described.Case report:This report describes the oral involvement with the formation of a deep ulceration, leading to communication between the oral and nasal cavities. Conclusion:Given the above, we reinforce the importance of an early diagnosis, made by an interdisciplinary team, in order to institute appropriate therapy and provide the patient with a longer survival.
publishDate 2020
dc.date.none.fl_str_mv 2020-08-31
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
RelCas
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicos.ufjf.br/index.php/hurevista/article/view/30171
10.34019/1982-8047.2020.v46.30171
url https://periodicos.ufjf.br/index.php/hurevista/article/view/30171
identifier_str_mv 10.34019/1982-8047.2020.v46.30171
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://periodicos.ufjf.br/index.php/hurevista/article/view/30171/21077
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Editora UFJF
publisher.none.fl_str_mv Editora UFJF
dc.source.none.fl_str_mv HU Revista; v. 46 (2020); 1-6
1982-8047
0103-3123
reponame:HU Revista (Online)
instname:Universidade Federal de Juiz de Fora (UFJF)
instacron:UFJF
instname_str Universidade Federal de Juiz de Fora (UFJF)
instacron_str UFJF
institution UFJF
reponame_str HU Revista (Online)
collection HU Revista (Online)
repository.name.fl_str_mv HU Revista (Online) - Universidade Federal de Juiz de Fora (UFJF)
repository.mail.fl_str_mv revista.hurevista@ufjf.edu.br
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