Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis

Detalhes bibliográficos
Autor(a) principal: MANDARIM DE LACERDA, MARIA ELENA
Data de Publicação: 2019
Outros Autores: Guimaraes, Leonardo Araujo, Souza, David de Almeida, Botelho, Lara Gomes, dos Santos, Julyane Alves de Assis, D’Oliveira, Leonardo Ferraz Marques
Tipo de documento: Artigo
Idioma: por
Título da fonte: Revista Científica da Faculdade de Medicina de Campos
Texto Completo: https://www.fmc.br/ojs/index.php/RCFMC/article/view/244
Resumo: ABSTRACT Described in 1937 by Friedrich Wegener, Granulomatosis with Polyangeitis (GPA) – formerly known as Wergener's granulomatosis – is a rare autoimmune condition. It is a vasculitis that affects small to medium vessels and necrotizing granulomatous inflammation. Vessels of great caliber are rarely affected. It attacks head and neck regions regularly. It has predilection for the upper respiratory tract, lungs and kidneys, however it can affect any organ. The ear, nose and throat regions are the most common in primary manifestations of the disease. Objective: To report the surgical approach to repairing nasal deformity in a patient diagnosed with GPA 25 years ago. Descriptions: Female patient, 41 years of age with diagnosis of GPA 25 years ago. She presented a picture of nasal deformity about 19 years ago. It presents collapse of the cartilaginous framework triggered by nasal septal necrosis. No functional complaints were reported. Scheduled open rhinoplasty with L neosepto preparation from costal cartilage graft. Currently, the patient has nasal tip support, complete reversal of the nose frame in the saddle, without functional complaints. Conclusion: GPA is a rare disease that in nasal attacks, septum perforation is a common event. Rarely, with a long time of illness, it can cause more extensive destruction of the nasal cartilage, generating deformities. This article presents a rare case of a patient with a long period of disease, presenting nasal deformity. A repair rhinoplasty with costal cartilage graft was performed. The surgery was performed at the Plastic Surgery Service of University Hospital Pedro Ernesto.
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spelling Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with PolyangiitisRinoplastia reparadora com enxerto de cartilagem costal em caso de necrose septal em paciente com Granilomatose com PoliangeiteCirurgia Plástica, Granulomatose com Poliangiite, Poliangiite Microscópica, RinoplastiaGranulomatosis with Polyangiitis, Microscopic Polyangiitis, Rhinoplasty, Plastic,SurgeryABSTRACT Described in 1937 by Friedrich Wegener, Granulomatosis with Polyangeitis (GPA) – formerly known as Wergener's granulomatosis – is a rare autoimmune condition. It is a vasculitis that affects small to medium vessels and necrotizing granulomatous inflammation. Vessels of great caliber are rarely affected. It attacks head and neck regions regularly. It has predilection for the upper respiratory tract, lungs and kidneys, however it can affect any organ. The ear, nose and throat regions are the most common in primary manifestations of the disease. Objective: To report the surgical approach to repairing nasal deformity in a patient diagnosed with GPA 25 years ago. Descriptions: Female patient, 41 years of age with diagnosis of GPA 25 years ago. She presented a picture of nasal deformity about 19 years ago. It presents collapse of the cartilaginous framework triggered by nasal septal necrosis. No functional complaints were reported. Scheduled open rhinoplasty with L neosepto preparation from costal cartilage graft. Currently, the patient has nasal tip support, complete reversal of the nose frame in the saddle, without functional complaints. Conclusion: GPA is a rare disease that in nasal attacks, septum perforation is a common event. Rarely, with a long time of illness, it can cause more extensive destruction of the nasal cartilage, generating deformities. This article presents a rare case of a patient with a long period of disease, presenting nasal deformity. A repair rhinoplasty with costal cartilage graft was performed. The surgery was performed at the Plastic Surgery Service of University Hospital Pedro Ernesto.Descrita em 1937, por Friedrich Wegener, a Granulomatose com Poliangeíte (GPA) – anteriormente conhecida como Granulomatose de Wergener – é uma condição autoimune rara. Trata-se de uma vasculite que acomete vasos de pequeno a médio calibre e inflamação granulomatosa necrotizante. Vasos de grande calibre raramente são afetados. Acomete regiões de cabeça e pescoço com regular frequência. Possui predileção pelo trato respiratório alto, pulmões e rins, no entanto pode acometer qualquer órgão. As regiões de orelha, nariz e garganta são as mais comuns em manifestações primárias da doença. Objetivo: Relatar a abordagem cirúrgica reparadora em quadro de deformidade nasal, em paciente com diagnóstico de GPA há 25 anos. Descrições: Paciente do sexo feminino, 41 anos de idade com diagnóstico de GPA há 25 anos. Apresenta quadro de deformidade nasal há aproximadamente 19 anos. Apresenta desabamento do arcabouço cartilaginoso desencadeada por necrose de septo nasal.  Não foram relatadas queixas funcionais. Programada rinoplastia aberta com confecção de neosepto em L a partir de enxerto de cartilagem costal. Atualmente a paciente apresenta sustentação da ponta nasal, reversão completa do quadro de nariz em sela, sem queixas funcionais. Conclusão: A GPA é uma doença rara que em acometimentos nasais a perfuração de septo é um evento comum. Raramente, com um longo tempo de doença, pode causar destruição mais extensa da cartilagem nasal, gerando deformidades. Este artigo apresenta um caso raro, de uma paciente com longo período de doença, apresentando deformidade nasal. Foi realizada rinoplastia reparadora com enxerto de cartilagem costal. A cirurgia foi realizada no Serviço de Cirurgia Plástica do Hospital Universitário Pedro Ernesto.Faculdade de Medicina de Campos (FMC)2019-06-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.fmc.br/ojs/index.php/RCFMC/article/view/24410.29184/1980-7813.rcfmc.244.vol.14.n1.2019Scientific Journal of the Medical School of Campos; Vol. 14 No. 1 (2019); 42-45Revista Científica da Faculdade de Medicina de Campos; v. 14 n. 1 (2019); 42-451980-7813reponame:Revista Científica da Faculdade de Medicina de Camposinstname:Faculdade de Medicina de Campos (FMC)instacron:FMCporhttps://www.fmc.br/ojs/index.php/RCFMC/article/view/244/189Copyright (c) 2019 Revista Científica da Faculdade de Medicina de Camposinfo:eu-repo/semantics/openAccessMANDARIM DE LACERDA, MARIA ELENAGuimaraes, Leonardo AraujoSouza, David de AlmeidaBotelho, Lara Gomesdos Santos, Julyane Alves de AssisD’Oliveira, Leonardo Ferraz Marques2021-01-06T19:41:35Zoai:ojs.www.fmc.br:article/244Revistahttps://www.fmc.br/ojs/index.php/RCFMC/PRIhttps://www.fmc.br/ojs/index.php/RCFMC/oai||revista@fmc.br1980-78131980-7813opendoar:2021-01-06T19:41:35Revista Científica da Faculdade de Medicina de Campos - Faculdade de Medicina de Campos (FMC)false
dc.title.none.fl_str_mv Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
Rinoplastia reparadora com enxerto de cartilagem costal em caso de necrose septal em paciente com Granilomatose com Poliangeite
title Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
spellingShingle Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
MANDARIM DE LACERDA, MARIA ELENA
Cirurgia Plástica, Granulomatose com Poliangiite, Poliangiite Microscópica, Rinoplastia
Granulomatosis with Polyangiitis, Microscopic Polyangiitis, Rhinoplasty, Plastic,Surgery
title_short Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
title_full Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
title_fullStr Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
title_full_unstemmed Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
title_sort Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
author MANDARIM DE LACERDA, MARIA ELENA
author_facet MANDARIM DE LACERDA, MARIA ELENA
Guimaraes, Leonardo Araujo
Souza, David de Almeida
Botelho, Lara Gomes
dos Santos, Julyane Alves de Assis
D’Oliveira, Leonardo Ferraz Marques
author_role author
author2 Guimaraes, Leonardo Araujo
Souza, David de Almeida
Botelho, Lara Gomes
dos Santos, Julyane Alves de Assis
D’Oliveira, Leonardo Ferraz Marques
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv MANDARIM DE LACERDA, MARIA ELENA
Guimaraes, Leonardo Araujo
Souza, David de Almeida
Botelho, Lara Gomes
dos Santos, Julyane Alves de Assis
D’Oliveira, Leonardo Ferraz Marques
dc.subject.por.fl_str_mv Cirurgia Plástica, Granulomatose com Poliangiite, Poliangiite Microscópica, Rinoplastia
Granulomatosis with Polyangiitis, Microscopic Polyangiitis, Rhinoplasty, Plastic,Surgery
topic Cirurgia Plástica, Granulomatose com Poliangiite, Poliangiite Microscópica, Rinoplastia
Granulomatosis with Polyangiitis, Microscopic Polyangiitis, Rhinoplasty, Plastic,Surgery
description ABSTRACT Described in 1937 by Friedrich Wegener, Granulomatosis with Polyangeitis (GPA) – formerly known as Wergener's granulomatosis – is a rare autoimmune condition. It is a vasculitis that affects small to medium vessels and necrotizing granulomatous inflammation. Vessels of great caliber are rarely affected. It attacks head and neck regions regularly. It has predilection for the upper respiratory tract, lungs and kidneys, however it can affect any organ. The ear, nose and throat regions are the most common in primary manifestations of the disease. Objective: To report the surgical approach to repairing nasal deformity in a patient diagnosed with GPA 25 years ago. Descriptions: Female patient, 41 years of age with diagnosis of GPA 25 years ago. She presented a picture of nasal deformity about 19 years ago. It presents collapse of the cartilaginous framework triggered by nasal septal necrosis. No functional complaints were reported. Scheduled open rhinoplasty with L neosepto preparation from costal cartilage graft. Currently, the patient has nasal tip support, complete reversal of the nose frame in the saddle, without functional complaints. Conclusion: GPA is a rare disease that in nasal attacks, septum perforation is a common event. Rarely, with a long time of illness, it can cause more extensive destruction of the nasal cartilage, generating deformities. This article presents a rare case of a patient with a long period of disease, presenting nasal deformity. A repair rhinoplasty with costal cartilage graft was performed. The surgery was performed at the Plastic Surgery Service of University Hospital Pedro Ernesto.
publishDate 2019
dc.date.none.fl_str_mv 2019-06-30
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dc.identifier.uri.fl_str_mv https://www.fmc.br/ojs/index.php/RCFMC/article/view/244
10.29184/1980-7813.rcfmc.244.vol.14.n1.2019
url https://www.fmc.br/ojs/index.php/RCFMC/article/view/244
identifier_str_mv 10.29184/1980-7813.rcfmc.244.vol.14.n1.2019
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv https://www.fmc.br/ojs/index.php/RCFMC/article/view/244/189
dc.rights.driver.fl_str_mv Copyright (c) 2019 Revista Científica da Faculdade de Medicina de Campos
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Revista Científica da Faculdade de Medicina de Campos
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dc.publisher.none.fl_str_mv Faculdade de Medicina de Campos (FMC)
publisher.none.fl_str_mv Faculdade de Medicina de Campos (FMC)
dc.source.none.fl_str_mv Scientific Journal of the Medical School of Campos; Vol. 14 No. 1 (2019); 42-45
Revista Científica da Faculdade de Medicina de Campos; v. 14 n. 1 (2019); 42-45
1980-7813
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