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  • Title: [Behcet's disease therapy review].
    Author: Vidaller Palacín A, Robert Olalla J, Sanuy Jiménez B, Rufi Rigau G, Folch Civit J, Charte González A.
    Journal: An Med Interna; 2002 Nov; 19(11):594-8. PubMed ID: 12522899.
    Abstract:
    Behçet's disease is an inflammatory process of unknown origin, which usually presents with recurrent oral ulcers, genital aphthae, uveitis and cutaneous lesions. However, a wide variety of clinical manifestations have been reported, and virtually any organ system may be affected, showing central nervous system, joints, blood vessels or gastrointestinal tract involvement. Therapeutic approach remains complex, and varies in basis of the affected organs. Complex aphthosis may respond to topical therapy, colchicine and dapsone. If this therapy does not result in adequate disease control, thalidomide, oral prednisone and methotrexate may be useful. When severe ocular lesions or systemic manifestations are present, therapies tend to be more aggressive, usually combining corticosteroids with immunosuppressive agents as cyclosporin, azathioprine, cyclophosphamide, interferon-alfa-2a, and chlorambucil.
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