PEDIATRICS · 1999 · 35 citations · 18 references
MedicineImmunologyPediatricsAutoimmunityImmunopathologyPediatric ImmunologyAutoimmune DiseasesImmune-mediated DiseaseImmunosuppressionImmunosuppressive AgentsImmunosuppressive TherapyPediatric VasculitisAphthous UlcerationChronic Relapsing DisorderCutaneous Blood VesselsGenital UlcersImmunosuppressed Patient ManagementImmunosuppressive Drug TherapyThalidomide AnalogsVasculitis Treatment
BACKGROUND: Behçet's syndrome is a chronic relapsing vasculitis characterized by aphthous stomatitis, genital ulcerations, and uveitis. The disease is a multisystem illness, which may involve the skin, joints, gastrointestinal tract, blood vessels, central nervous system, and other organs. CASE STUDY: We report a case of an infant with features of Behçet's syndrome who did not respond to conventional immunosuppression with high-dose corticosteroids and cytotoxic agents. Thalidomide, a potent immune response-modifying drug, was used with marked improvement and resolution of symptoms. CONCLUSION: This finding supports a trial of thalidomide treatment in patients with Behçet's syndrome who are unresponsive to other forms of immunosuppressive therapy or develop undesirable side effects.
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Criteria for diagnosis of Behçet's disease
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Thalidomide is an inhibitor of angiogenesis.
Robert J. D’Amato, Michael Loughnan, Evelyn Flynn et al. · Proceedings of the National Academy of Sciences · 1994 · 2.5K citations
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M Hamza, A Zribi, Ben Ayed H · PubMed · 1976 · 1.1K citations
Criteria for diagnosis of Behcet's disease
INTERNATIONALSTUDYGROUPFORBEHC · The Lancet · 1990 · 682 citations