Template:Primary Vasculitis DDX: Difference between revisions
| Line 1: | Line 1: | ||
===[[Vasculitis syndromes| | ===[[Vasculitis syndromes|Vasculitis Syndrome Types]]=== | ||
*Large vessel | *Large vessel | ||
**[[Takayasu arteritis]] | **[[Takayasu arteritis]] | ||
**[[Giant cell arteritis]] | **[[Giant cell arteritis]] (temporal arteritis) | ||
*Medium vessel | *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]] | **[[Polyarteritis nodosa]] | ||
**[[Thromboangiitis obliterans]] (Buerger's disease) | **[[Thromboangiitis obliterans]] (Buerger's disease) | ||
**Microscopic polyangiitis | **Microscopic polyangiitis | ||
*Small vessel | *Small vessel | ||
| Line 14: | Line 15: | ||
**[[Henoch-Schonlein purpura]] | **[[Henoch-Schonlein purpura]] | ||
**[[Behçet's disease]] | **[[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]] | |||
*Secondary vasculitides and other/miscellaneous | |||
**Drug-induced vasculitis | |||
**[[Serum sickness]] | |||
**Vasculitis associated with other rheumatic diseases (e.g. [[SLE]]) | |||
Revision as of 17:56, 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)