Eosinophilic granulomatosis with polyangiitis misdiagnosed as non-ST-segment elevation myocardial infarction: A case report

Y. Oh, Miyeun Han, Hye-Kyung Park, Eun-Jung Jo
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Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic disease and a potentially life‐threatening systemic necrotiz-ing vasculitis predominantly affecting small vessels. Herein, we describe a 47-year-old man with EGPA misdiagnosed as non-ST-seg-ment elevation myocardial infarction. He presented to the Emergency Department with indigestion and diarrhea. He had been diagnosed with asthma and chronic rhinosinusitis 3 years earlier and was taking antibiotics due to worsening sinusitis. In laboratory tests, peripheral blood eosinophils, serum creatinine, and serum troponin were elevated to 4,641 cells/μL, 13.40 ng/mL, and 1.26 ng/ mL, respectively. Electrocardiography showed ST-segment depression on the inferior wall, and echocardiography indicated an isch-emic insult in the right coronary artery territory. A non-ST-segment elevation myocardial infarction as well as antibiotic-associated diarrhea, eosinophilia and acute kidney injury was initially suspected. However, fever persisted and eosinophilia worsened despite cessation of antibiotics after admission. There was no significant stenosis of the coronary arteries on coronary angiography. Mean-while, abdominal computed tomography suggested medical renal disease, and magnetic resonance imaging showed late gadolinium enhancement at the mid wall and the subepicardial area in the left ventricle of the heart. As a workup for eosinophilia, serum anti-MPO was measured and turned out to be positive. A kidney biopsy was performed, which yielded membranous nephropathy superimposed on antineutrophil cytoplasmic antibodies-mediated crescent formation. He was diagnosed as EGPA with cardiac and renal involvement, and received systemic steroid, cyclophosphamide, and plasmapheresis. Then, peripheral eosinophil counts and renal function were normalized. He is now in clinical remission even after stopping the use of steroids and immunosuppressive agents. ( Allergy Asthma Respir Dis 2021;9:50-55 )
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嗜酸性肉芽肿病合并多血管炎误诊为非st段抬高型心肌梗死1例
嗜酸性肉芽肿病合并多血管炎(EGPA)是一种罕见的全身性疾病,是一种主要影响小血管的潜在危及生命的系统性坏死性血管炎。在此,我们描述了一个47岁的男性EGPA误诊为非st段抬高心肌梗死。他因消化不良和腹泻到急诊科就诊。3年前,他被诊断出患有哮喘和慢性鼻窦炎,由于鼻窦炎恶化,他正在服用抗生素。在实验室检查中,外周血嗜酸性粒细胞、血清肌酐和血清肌钙蛋白分别升高至4,641个细胞/μL、13.40 ng/mL和1.26 ng/mL。心电图显示下壁st段凹陷,超声心动图显示右冠状动脉区缺血性损伤。最初怀疑为非st段抬高型心肌梗死以及抗生素相关性腹泻、嗜酸性粒细胞增多和急性肾损伤。然而,尽管入院后停用抗生素,发烧仍持续存在,嗜酸性粒细胞增多恶化。冠状动脉造影未见明显冠状动脉狭窄。腹部ct提示内科肾病,磁共振示左心室中壁及心外膜下晚期钆增强。作为嗜酸性粒细胞增多症的检查,测定血清抗mpo呈阳性。进行肾活检,发现膜性肾病叠加抗中性粒细胞胞质抗体介导的新月形成。他被诊断为EGPA并累及心脏和肾脏,并接受了全身类固醇、环磷酰胺和血浆置换。外周血嗜酸性粒细胞计数和肾功能恢复正常。即使在停止使用类固醇和免疫抑制剂后,他现在仍处于临床缓解期。(过敏哮喘呼吸疾病2021;9:50-55)
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