Abstract
Sulfasalazine (SSZ) can induce serological and clinical autoimmune reactions but the occurrence of SSZ-related Wegener's granulomatosis (WG) has not been reported before. We describe two patients with rheumatoid factor (RF)-positive rheumatoid arthritis (RA) who developed biopsy-proven WG with serious organ involvement during SSZ therapy. The pathogenetic mechanism that explains the relationship between SSZ and the occurrence of a de novo anti-neutrophil cytoplasmic antibody (ANCA)-related vasculitis or a flare is discussed. We propose that WG can be a rare complication of SSZ therapy and that this, like other autoimmune adverse events of this drug, is mediated by SSZ-induced apoptosis.
Original language | English |
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Pages (from-to) | 72-4 |
Number of pages | 3 |
Journal | Scandinavian Journal of Rheumatology |
Volume | 37 |
Issue number | 1 |
DOIs | |
Publication status | Published - 15 Jan 2008 |
Keywords
- Adult
- Aged
- Antirheumatic Agents
- C-Reactive Protein
- Cyclophosphamide
- Disease Progression
- Glucocorticoids
- Granulomatosis with Polyangiitis
- Humans
- Methylprednisolone
- Sulfasalazine