Granulomatosis with polyangiitis: case report with oral involvement
Autor(a) principal: | |
---|---|
Data de Publicação: | 2020 |
Outros Autores: | , , , |
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. |
id |
UFJF-8_5c59ceb739cd85c99c6e41acf0665c15 |
---|---|
oai_identifier_str |
oai:periodicos.ufjf.br:article/30171 |
network_acronym_str |
UFJF-8 |
network_name_str |
HU Revista (Online) |
repository_id_str |
|
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 |
_version_ |
1796798243870343168 |