Review Article
Microscopic Polyangiitis in Systemic Sclerosis
Table 3
Differences in vascular clinical findings between SSc and MPA.
| | SSc | MPA |
| Raynaud’s phenomenon | | | digital ischemia | | | skin ulcers | | | skin nodules | | | Purpura | | | nail bed change/telangiectasia | | | Myositis | | | interstitial pneumonia | | | honeycomb lung | | | alveolar hemorrhage | | | pulmonary hypertension | | | RPGN | | | scleroderma renal crisis | | | mononeuritis multiplex | | | CNS vasculitis | | | Histological findings; | | | fibrinoid necrosis | arteries, arterioles | capillaries, arterioles | intimal hyperplasia | | | capillaritis | | | pFNCGN | | |
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SSc: scleroderma MPA: microscopic polyangiitis RPGN: rapidly progressive glomerulonephritis CNS: central nervous system pFNCGN: pauci-immune focal necrotizing crescentic glomerulonephritis.
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