A case of ANCA-associated vasculitis presenting with calf claudication

• DOI: 10.1007/s00296-010-1469-3
• Publication Date: 2010-04-03T11:36:00Z
• Authors: Mi Yeon Kim; Sun Youn Bae; Mirae Lee; Hojung Chung; Jaejoon Lee; Joong Kyong Ahn; Hoon-Suk Cha; Eun-Mi Koh
• Keywords: Claudication; Necrotizing Vasculitis; Microscopic polyangiitis; Skin biopsy

Wegener's granulomatosis (WG), Churg-Strauss syndrome, and microscopic polyangiitis (MPA) are closely related small vessel vasculitides characterized by anti-neutrophil cytoplasmic antibodies (ANCA). Although there were some reports of MPA presenting with claudication, there are very few reports on WG presenting with claudication of calf muscles. We report an unusual case of ANCA-associated vasculitis in a 75-year-old man who presented with bilateral calf claudication. Comprehensive evaluations, including electromyography, nerve conduction study, lower extremity magnetic resonance imaging, and Doppler scan, did not reveal any other cause of bilateral calf claudication. P-ANCA and anti-myeloperoxidase antibody was positive, but the anti-proteinase 3 antibody was negative. Chest computed tomography scan showed subpleural honeycombing and reticulation, predominantly in both basal lung areas. Biopsy of the calf muscle showed granulomatous vasculitis. Kidney biopsy was also performed which revealed focal necrotizing glomerulonephritis. Our patient does not exhibit typical clinical features for WG, but histopathologic findings of necrotizing granulomatous vasculitis in calf muscle biopsy is highly suggestive of WG.