A Case of Improved Refractory Uveitis in Behcet's Disease after Infliximab Therapy / 대한류마티스학회지
The Journal of the Korean Rheumatism Association
; : 320-323, 2005.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-84599
Biblioteca responsável:
WPRO
ABSTRACT
Behcet's disease is a multisystemic, chronic relapsing inflammatory disease characterized by vasculitides, mucocutaneous lesions, thrombophlebitis, arthritis. Among them, the ocular involvement is usual (50~70%) and the most serious morbidity is blindness (20~25% of those of affected). Immunosuppressive treatment is currently the main therapy in chronic relapsing uveitis, but many patients experience recurrent sight-threatening uveitis. T lymphocytes play an important role in the pathogenesis of uveitis by releasing cytokines such as tumor necrosis factor (TNF) alpha. There are some reports that the anti-TNFalpha treatment is effective in refractory Behcet's uveitis, but it has not been reported in Korea. We report a case of refractory uveitis in Behcet's disease which is improved after anti-TNFalpha therapy.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Artrite
/
Tromboflebite
/
Uveíte
/
Vasculite
/
Linfócitos T
/
Cegueira
/
Citocinas
/
Fator de Necrose Tumoral alfa
/
Infliximab
/
Coreia (Geográfico)
Limite:
Humanos
País/Região como assunto:
Ásia
Idioma:
Coreano
Revista:
The Journal of the Korean Rheumatism Association
Ano de publicação:
2005
Tipo de documento:
Artigo