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A Case of Improved Refractory Uveitis in Behcet's Disease after Infliximab Therapy / 대한류마티스학회지
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.
Assuntos

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
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
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