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An incomplete form of childhood Behçet's disease treated with infliximab.
Caporuscio, S; Pranteda, G; Nistico, S; Maucione, T; Canzoni, M; Stefani, A; Muscianese, M; Fanto, M; Sorgi, M.
Afiliación
  • Caporuscio S; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Pranteda G; Division of Dermatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Nistico S; Unit of Dermatology, University of Catanzaro, Italy.
  • Maucione T; Sapienza University of Rome, Rome, Italy.
  • Canzoni M; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Stefani A; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Muscianese M; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Fanto M; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
  • Sorgi M; Division of Rheumatology, Department of Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
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
Buscar en Google
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