Colitis as the Initial Presentation of Eosinophilic Granulomatosis with Polyangiitis.

Case Reports in Rheumatology Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI:10.1155/2023/6620826
Sharika Gopakumar Menon, Steven Hugenberg, Ahmad M Alkashash, Jingmei Lin, Arya M Iranmanesh
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Abstract

A male patient in his early sixties with recurrent diarrhea was transferred to our hospital. The patient did not have any pulmonary or upper respiratory symptoms. He was noted to have peripheral eosinophilia. Further workup revealed a negative antineutrophilic cytoplasmic antibody titer but a positive myeloperoxidase antibody and positive proteinase 3 antibodies. A colon biopsy also revealed eosinophilic-rich granulomas in the mucosa, confirming a diagnosis of eosinophilic granulomatosis with polyangiitis. On cardiac imaging, eosinophilic myocarditis was also discovered. To treat active severe EGPA, the patient received high-dose corticosteroids and intravenous cyclophosphamide. The occurrence of gastrointestinal involvement as an initial manifestation of eosinophilic granulomatosis with polyangiitis is infrequent, emphasizing the significance of its recognition. This case underscores the importance of identifying and diagnosing such atypical presentations to facilitate timely and appropriate management.

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结肠炎是嗜酸性粒细胞增多症合并多血管炎的最初表现。
一名60出头的男性患者因反复腹泻被转移到我们医院。患者没有任何肺部或上呼吸道症状。他被发现有外周嗜酸性粒细胞增多症。进一步的检查显示抗中性粒细胞细胞质抗体滴度为阴性,但髓过氧化物酶抗体和蛋白酶3抗体为阳性。结肠活检还显示粘膜中有嗜酸性粒细胞丰富的肉芽肿,证实了嗜酸性肉芽肿伴多血管炎的诊断。在心脏影像学上,还发现了嗜酸性粒细胞性心肌炎。为了治疗活动性严重EGPA,患者接受了高剂量皮质类固醇和环磷酰胺静脉注射。胃肠道受累是嗜酸性肉芽肿伴多血管炎的最初表现,这种情况很少发生,强调了对其认识的重要性。该病例强调了识别和诊断此类非典型表现以促进及时和适当管理的重要性。
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