Extensive ischaemic colitis-like colonic lesions in eosinophilic granulomatosis with polyangiitis.

Yoshitaka Ueda, Kota Shimada
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Abstract

Eosinophilic granulomatosis with polyangiitis is a rare, immune-mediated, multisystemic disorder belonging to the group of antineutrophil cytoplasmic antibody-associated vasculitides. Gastrointestinal symptoms are relatively common in patients with eosinophilic granulomatosis with polyangiitis, reportedly occurring in ∼22.3% of cases. Vasculitic necrotising lesions normally occur in the intestinal tract, and in the present case, the colonic lesions were remarkably severe and extensive. Pulse steroid therapy combined with cyclophosphamide improved the patient's condition without any serious complications, such as intestinal perforation.

嗜酸性粒细胞肉芽肿伴多血管炎的广泛缺血性结肠炎样结肠病变。
嗜酸性粒细胞肉芽肿伴多血管炎是一种罕见的免疫介导的多系统疾病,属于抗中性粒细胞胞浆抗体相关性血管炎。胃肠道症状在嗜酸性粒细胞肉芽肿伴多血管炎患者中较为常见,据报道有 22.3%的病例会出现胃肠道症状。血管性坏死病变通常发生在肠道,在本病例中,结肠病变明显严重且范围广泛。脉冲类固醇治疗联合环磷酰胺改善了患者的病情,没有出现肠穿孔等严重并发症。
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