Therapy of resistant systemic necrotizing vasculitis. Polyarteritis, Churg-Strauss syndrome, Wegener's granulomatosis, and hypersensitivity vasculitis group disorders

Rheum Dis Clin North Am. 1995 Feb;21(1):41-57.

Abstract

The systemic necrotizing vasculitides represent a difficult group of diseases from a therapeutic perspective. Even with successful therapy patients often experience a high degree of disease and treatment morbidity. Refractory disease, or that which fails to respond to standard therapy, is particularly challenging. A clinical approach to several vasculitic syndromes is outlined in this article with emphasis given to therapies supported by controlled investigations and those supported by consensus opinion where available.

Publication types

  • Review

MeSH terms

  • Churg-Strauss Syndrome / drug therapy*
  • Drug Resistance
  • Granulomatosis with Polyangiitis / diagnosis
  • Granulomatosis with Polyangiitis / drug therapy*
  • Humans
  • Polyarteritis Nodosa / drug therapy*
  • Vasculitis, Leukocytoclastic, Cutaneous / drug therapy*