Template:Primary Vasculitis DDX: Difference between revisions
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**[[Henoch-Schonlein purpura]] | **[[Henoch-Schonlein purpura]] | ||
**[[Behçet's disease]] | **[[Behçet's disease]] | ||
**ANCA-associated vasculitides: | **ANCA-associated vasculitides: | ||
Revision as of 18:15, 2 August 2023
Vasculitis Syndrome Types
- Large vessel
- Takayasu arteritis
- Giant cell arteritis (temporal arteritis)
- Medium vessel
- Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)
- Granulomatosis with polyangiitis (Wegener's granulomatosis)
- Kawasaki disease
- Primary angiitis of the central nervous system
- Polyarteritis nodosa
- Thromboangiitis obliterans (Buerger's disease)
- Microscopic polyangiitis
- Small vessel
- Essential mixed cryoglobulinemia
- Henoch-Schonlein purpura
- Behçet's disease
- ANCA-associated vasculitides:
- Granulomatosis with polyangiitis (Wegner's)
- Eosinophilic granulomatosis with polyangiitis (Churg-Strauss)
- Microscopic polyangiitis
- Cutaneous leukocytoclastic angiitis (“hypersensitivity vasculitis”)
- Essential cryoglobulinemia, cryoglobulinemic vasculitis due to hepatitis C
- Behcet's disease
- ANCA-associated vasculitides:
- Secondary vasculitides and other/miscellaneous
- Drug-induced vasculitis
- Serum sickness
- Vasculitis associated with other rheumatic diseases (e.g. SLE)