以皮肤损害为首发表现的嗜酸性肉芽肿性多血管炎一例

doi:10.12144/zgmfskin202607524

China Journal of Leprosy and Skin Diseases ›› 2026, Vol. 42 ›› Issue (7): 524-526.doi: 10.12144/zgmfskin202607524

• Case Reports • Previous Articles Next Articles

Eosinophilic granulomatosis with polyangiitis presenting with initial skin lesions: a case report

ZHANG Yuanbin, LI Jinghuan, AI Dongfang, FENG Shijun

Department of Dermatology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou 061000, China

Online:2026-07-15 Published:2026-06-29

Abstract

Abstract: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic necrotizing vasculitis with highly heterogeneous clinical manifestations, and only about 14% of patients present with skin lesions as the initial symptom. This paper reports a case of EGPA with skin lesions as the initial manifestation and positive anti-glomerular basement membrane (anti-GBM) antibodies.

Key words: eosinophilic granulomatosis with polyangiitis, skin onset, purpura, eosinophil, anti-GBM antibody

ZHANG Yuanbin, LI Jinghuan, AI Dongfang, FENG Shijun. Eosinophilic granulomatosis with polyangiitis presenting with initial skin lesions: a case report[J].China Journal of Leprosy and Skin Diseases, 2026, 42(7): 524-526.

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Eosinophilic granulomatosis with polyangiitis presenting with initial skin lesions: a case report

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