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Table 1 Vasculitis entities eligible for inclusion in the GeVas registry

From: The Joint Vasculitis Registry in German-speaking countries (GeVas) – a prospective, multicenter registry for the follow-up of long-term outcomes in vasculitis

Vasculitis entities
1. Large vessel vasculitis
 • Giant Cell Arteritis
 • Takayasu Arteritis
2. Medium size vessel vasculitis
 • Polyarteritis nodosa
 • Kawasaki disease
3. Small vessel vasculitis
ANCA-associated vasculitides
  • Microscopic Polyangiitis
  • Granulomatosis with Polyangiitis
  • Eosinophilic Granulomatosis with Polyangiitis
Immune complex vasculitis
  • Anti-GBM(glomerular basement membrane) disease
  • Cryoglobulinemic vasculitis
  • IgA vasculitis
  • Hypocomplementemic urticarial vasculitis (Anti-C1q vasculitis)
4. Variable Vessel Vasculitis
 • Behcet’s disease
 • Cogan’s Syndrome
5. Single Organ Vasculitis
 • Cutaneous (leukocytoclastic) small vessel vasculitis
 • Cutaneous arteritis
 • Primary central nervous system vasculitis
 • Isolated aortitis
 • Others
6. Vasculitis associated with systemic disease
 • Lupus vasculitis
 • Rheumatoid vasculitis
 • Sarcoid vasculitis
 • Others
7. Vasculitis associated with probable etiology
 • Hepatitis C virus-associated cryoglobulinemic vasculitis
 • Hepatitis B virus-associated polyarteritis nodosa
 • Syphilis-associated vasculitis
 • Drug-associated immune complex vasculitis
 • Drug-associated ANCA-associated vasculitis
 • Cancer-associated vasculitis
 • Others