a Department of Internal Medicine and Rheumatology , Juntendo University Urayasu Hospital , Chiba , Japan.
b Institute for Environmental and Gender Specific Medicine, Juntendo University School of Medicine , Chiba , Japan.
Mod Rheumatol. 2016 Nov;26(6):968-970. doi: 10.3109/14397595.2014.940126. Epub 2014 Aug 11.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a disorder characterized by extravascular granulomas, hypereosinophilia, and pulmonary and systemic small-vessel vasculitis. Bowel perforation is a rare but often fatal complication of EGPA. In the present report, we describe a case of small intestinal perforation in a patient with EGPA. Through various examinations, we confirmed the presence of EGPA, and the patient responded well to steroid therapy. However, as the patient's condition subsequently worsened, the small intestine was consequently resected. The patient's overall condition improved thereafter. Thus, we believe that careful attention should be paid to intestinal symptoms and perforation in patients with EGPA.
嗜酸性肉芽肿性多血管炎(EGPA)是一种以血管外肉芽肿、嗜酸性粒细胞增多和肺及全身小血管炎为特征的疾病。肠穿孔是 EGPA 的一种罕见但常致命的并发症。本报告描述了一例 EGPA 患者的小肠穿孔病例。通过各种检查,我们证实了 EGPA 的存在,且患者对类固醇治疗反应良好。然而,由于患者病情随后恶化,随后对小肠进行了切除。此后,患者的整体状况得到改善。因此,我们认为应密切关注 EGPA 患者的肠道症状和穿孔。