Menon Sharika Gopakumar, Hugenberg Steven, Alkashash Ahmad M, Lin Jingmei, Iranmanesh Arya M
Department of Medicine, Rheumatology Division, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Case Rep Rheumatol. 2023 Oct 9;2023:6620826. doi: 10.1155/2023/6620826. eCollection 2023.
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.
一名60岁出头、反复腹泻的男性患者被转至我院。该患者无任何肺部或上呼吸道症状。检查发现其外周血嗜酸性粒细胞增多。进一步检查显示抗中性粒细胞胞浆抗体滴度为阴性,但髓过氧化物酶抗体和蛋白酶3抗体呈阳性。结肠活检还显示黏膜中有富含嗜酸性粒细胞的肉芽肿,确诊为嗜酸性肉芽肿性多血管炎。心脏成像检查还发现了嗜酸性粒细胞性心肌炎。为治疗活动性重症嗜酸性肉芽肿性多血管炎,该患者接受了大剂量糖皮质激素和静脉注射环磷酰胺治疗。嗜酸性肉芽肿性多血管炎以胃肠道受累为首发表现的情况并不常见,这凸显了识别该病的重要性。该病例强调了识别和诊断此类非典型表现以促进及时、恰当治疗的重要性。