The clinical chameleon: eosinophilic myocarditis presenting as acute coronary syndrome-a case report.

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
European Heart Journal: Case Reports Pub Date : 2026-10-12 eCollection Date: 2026-10-01 DOI:10.1093/ehjcr/ytag752
Denise Belén Magnifico, Ignacio Melem, Sergio Baratta, Renzo Melchiori
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引用次数: 0

Abstract

Background: Eosinophilic myocarditis is a rare inflammatory cardiomyopathy that may clinically mimic acute coronary syndrome and should be considered in patients with non-obstructive coronary arteries, often resulting in diagnostic delay.

Case summary: A 27-year-old man presented with recurrent chest pain and was initially misdiagnosed with a panic attack. On admission, laboratory evaluation revealed marked peripheral eosinophilia (1800/mm3), mildly elevated troponin, and increased serum IgE levels. Echocardiography demonstrated reduced left ventricular ejection fraction and a large apical intracavitary thrombus. Coronary angiography revealed normal coronary arteries. Cardiac magnetic resonance imaging showed myocardial oedema and circumferential subendocardial late gadolinium enhancement consistent with eosinophilic myocarditis. Extensive aetiological workup was negative. Although endomyocardial biopsy showed non-specific findings, the diagnosis was established through multimodal integration of clinical, imaging, and laboratory data. High-dose corticosteroid therapy and anticoagulation resulted in rapid clinical improvement, recovery of ventricular function, and near-complete thrombus resolution.

Discussion: Eosinophilic myocarditis should be considered in young patients presenting with chest pain and non-obstructive coronary arteries. Multimodality imaging-particularly cardiac magnetic resonance-plays a key role in diagnosis, while early corticosteroid therapy may lead to rapid clinical and functional recovery.

Conclusion: This case underscores the importance of maintaining a high index of clinical suspicion for EM in young patients presenting with chest pain and peripheral eosinophilia. A multimodal diagnostic approach integrating cMRI findings, laboratory data, and exclusion of alternative aetiologies is essential when biopsy results are inconclusive. Early immunosuppressive therapy is key to reversing myocardial damage and preventing progression to end-stage heart failure.

临床变色龙:嗜酸性心肌炎表现为急性冠脉综合征1例。
背景:嗜酸性心肌炎是一种罕见的炎症性心肌病,临床上可能与急性冠状动脉综合征相似,在非阻塞性冠状动脉患者中应予以考虑,常导致诊断延误。病例总结:一名27岁的男性表现为复发性胸痛,最初被误诊为惊恐发作。入院时,实验室评估显示明显的外周嗜酸性粒细胞增多(1800/mm3),肌钙蛋白轻度升高,血清IgE水平升高。超声心动图显示左心室射血分数降低和一个大的根尖腔内血栓。冠状动脉造影显示冠状动脉正常。心脏磁共振成像显示心肌水肿和心内膜下周性晚期钆增强与嗜酸性心肌炎一致。广泛的病因检查结果为阴性。虽然心内膜活检显示非特异性结果,但通过临床、影像学和实验室数据的多模式整合建立了诊断。大剂量皮质类固醇治疗和抗凝治疗可迅速改善临床,恢复心室功能,并几乎完全消除血栓。讨论:以胸痛和非阻塞性冠状动脉为表现的年轻患者应考虑嗜酸性心肌炎。多模态成像(尤其是心脏磁共振)在诊断中起着关键作用,而早期皮质类固醇治疗可能会导致快速临床和功能恢复。结论:该病例强调了在以胸痛和外周嗜酸性粒细胞增多为表现的年轻EM患者中保持高临床怀疑指数的重要性。当活检结果不确定时,综合cMRI结果、实验室数据和排除其他病因的多模式诊断方法是必不可少的。早期免疫抑制治疗是逆转心肌损伤和防止进展为终末期心力衰竭的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Heart Journal: Case Reports
European Heart Journal: Case Reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
10.00%
发文量
451
审稿时长
14 weeks
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