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Successful Treatment of Child Neuro-Behcet's Disease with Infliximab
Journal of Rheumatic Diseases ; : 209-213, 2014.
Article in Korean | WPRIM | ID: wpr-190174
ABSTRACT
Behcet's disease is a systemic vasculitis, characterized by recurrent oral aphthous ulcers, recurrent genital ulcers, skin lesion, and ocular involvement. Monoclonal antibody to the tumor necrosis factor-alpha (TNF-alpha) is considered as a possible therapeutic approach to achieve clinical improvement, preventing relapse in Behcet's disease refractory to conventional anti-inflammatory drugs or immunosuppressive durgs. We report the use of infliximab, which is one of the TNF-alpha monoclonal antibodies, in a 17-year-old girl with Behcet's disease exhibiting severe mucocutaneous, ocular and neurological involvement refractory to standard treatment.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Recurrence / Skin Ulcer / Stomatitis, Aphthous / Tumor Necrosis Factor-alpha / Systemic Vasculitis / Infliximab / Antibodies, Monoclonal Limits: Adolescent / Child / Female / Humans Language: Korean Journal: Journal of Rheumatic Diseases Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Recurrence / Skin Ulcer / Stomatitis, Aphthous / Tumor Necrosis Factor-alpha / Systemic Vasculitis / Infliximab / Antibodies, Monoclonal Limits: Adolescent / Child / Female / Humans Language: Korean Journal: Journal of Rheumatic Diseases Year: 2014 Type: Article