Coexistence of relapsing polychondritis and eosinophilic granulomatous with polyangiitis: A rare entity.
Clin Ter
; 173(6): 500-502, 2022.
Article
em En
| MEDLINE
| ID: mdl-36373442
ABSTRACT
Abstract Relapsing polychondritis (RP) is a a rare multisystemic disease and it affects cartilaginous tissue and proteoglycan rich organs. The spectrum of clinical features are intermittent inflammation involving especially the auricular and nasal regions. In some patients with RP, systemic vasculitis, autoimmune diseases or malignancy may accompany. Although rare, any of the ANCA-associated vasculitis have been reported in patients with RP. Eosinophilic granulomatous with polyangiitis (EGPA) is a multisystem small vessel vasculitis associated with asthma and eosinophilia. Here we present a case of coexistence of RP and EGPA.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Policondrite Recidivante
/
Asma
/
Doenças Autoimunes
/
Vasculite Sistêmica
Tipo de estudo:
Diagnostic_studies
Limite:
Humans
Idioma:
En
Revista:
Clin Ter
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
Turquia