Repairing rhinoplasty with costal cartilage graft in case of septal necrosis in a patient with Granilomatosis with Polyangiitis
Autor(a) principal: | |
---|---|
Data de Publicação: | 2019 |
Outros Autores: | , , , , |
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. |
id |
FMC-0_4278d7498fac167d58fb795e3f0e8584 |
---|---|
oai_identifier_str |
oai:ojs.www.fmc.br:article/244 |
network_acronym_str |
FMC-0 |
network_name_str |
Revista Científica da Faculdade de Medicina de Campos |
repository_id_str |
|
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 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
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 |
language |
por |
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 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
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 reponame:Revista Científica da Faculdade de Medicina de Campos instname:Faculdade de Medicina de Campos (FMC) instacron:FMC |
instname_str |
Faculdade de Medicina de Campos (FMC) |
instacron_str |
FMC |
institution |
FMC |
reponame_str |
Revista Científica da Faculdade de Medicina de Campos |
collection |
Revista Científica da Faculdade de Medicina de Campos |
repository.name.fl_str_mv |
Revista Científica da Faculdade de Medicina de Campos - Faculdade de Medicina de Campos (FMC) |
repository.mail.fl_str_mv |
||revista@fmc.br |
_version_ |
1798042301933551616 |