An incomplete form of childhood Behçet's disease treated with infliximab.
Int J Immunopathol Pharmacol
; 27(3): 445-8, 2014.
Article
en En
| MEDLINE
| ID: mdl-25280037
ABSTRACT
Behçet's disease (BD) is a multi-systemic vasculitis characterized by the possible presence of cutaneous, ocular, articular and neurological manifestations. In this report, we examine the case of a fifteen-year old boy with an incomplete form of juvenile Behçet's disease which began with joint involvement and developed into a complete form only after several years. The patient showed a rapid response to anti-TNF-alpha (infliximab) with an improvement of mucocutaneous lesions (oral and genital ulcers, pseudofolliculitis) and arthritis.
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Bases de datos:
MEDLINE
Asunto principal:
Síndrome de Behçet
/
Anticuerpos Monoclonales
Tipo de estudio:
Diagnostic_studies
Límite:
Adolescent
/
Humans
/
Male
Idioma:
En
Revista:
Int J Immunopathol Pharmacol
Asunto de la revista:
ALERGIA E IMUNOLOGIA
/
FARMACOLOGIA
/
PATOLOGIA
Año:
2014
Tipo del documento:
Article
País de afiliación:
Italia