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A case of severe MAGIC syndrome treated successfully with the tumor necrosis factor-alpha inhibitor infliximab.

Abstract
We report a patient with an overlap of relapsing polychondritis and Behcet disease whose cartilaginous inflammation and genital lesions were refractory to corticosteroids and immunosuppressants, but fully remitted with the tumor necrosis factor-alpha inhibitor, infliximab. We believe this case represents the first report of a response to a tumor necrosis factor inhibitor in a patient with mouth and genital ulcerations with inflamed cartilage syndrome.
AuthorsErik D Geissal, Richard Wernick
JournalJournal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases (J Clin Rheumatol) Vol. 16 Issue 4 Pg. 185-7 (Jun 2010) ISSN: 1536-7355 [Electronic] United States
PMID20414125 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal
  • Tumor Necrosis Factor-alpha
  • Infliximab
Topics
  • Adult
  • Anti-Inflammatory Agents (therapeutic use)
  • Antibodies, Monoclonal (therapeutic use)
  • Behcet Syndrome (complications, drug therapy)
  • Humans
  • Infliximab
  • Male
  • Polychondritis, Relapsing (complications, drug therapy)
  • Remission Induction
  • Syndrome
  • Tumor Necrosis Factor-alpha (antagonists & inhibitors)

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