Successful Treatment of Child Neuro-Behcet's Disease with Infliximab
Journal of Rheumatic Diseases
; : 209-213, 2014.
Article
de Ko
| WPRIM
| ID: wpr-190174
Bibliothèque responsable:
WPRO
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.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Récidive
/
Ulcère cutané
/
Stomatite aphteuse
/
Facteur de nécrose tumorale alpha
/
Vascularite systémique
/
Infliximab
/
Anticorps monoclonaux
Limites du sujet:
Adolescent
/
Child
/
Female
/
Humans
langue:
Ko
Texte intégral:
Journal of Rheumatic Diseases
Année:
2014
Type:
Article