嗜酸性粒细胞性心肌炎:诊断难题与治疗困境--病例报告

Z. Ammouri, S. Belkouchia, I. Rezzouk, S. moussaoui, R. Habbal
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引用次数: 0

摘要

嗜酸性粒细胞性心肌炎是一种罕见且可能危及生命的疾病,它可能与急性冠状动脉综合征(ACS)相似,给诊断带来困难。 我们描述了一名 32 岁男子的病例,他最初因出现类似 ACS 的症状入院,但最终被诊断为嗜酸性粒细胞性心肌炎。嗜酸性粒细胞过多综合征(Hypereosinophilic Syndrome)包括多种血液疾病,其特点是持续性、原因不明的嗜酸性粒细胞过多导致组织损伤。约 20% 的嗜酸性粒细胞过多综合征病例会累及心脏,这标志着一个关键阶段的到来。 我们的报告强调了在评估胸痛和嗜酸性粒细胞过多症患者时考虑嗜酸性粒细胞性心肌炎和 SHI 的重要性。它强调了诊断的微妙性以及早期识别和适当治疗的必要性,以改善嗜酸性粒细胞性心肌炎病例的预后。本病例强调了心肌炎的多种临床表现,以及在出现胸痛和嗜酸性粒细胞过多时采取综合诊断方法的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eosinophilic Myocarditis: A Diagnostic Challenge and Treatment Dilemma - A Case Report
Eosinophilic myocarditis, a rare and potentially life-threatening condition, can resemble acute coronary syndrome (ACS) and presents diagnostic difficulties. We describe the case of a 32-year-old man initially admitted with ACS-like symptoms, but ultimately diagnosed with eosinophilic myocarditis. Hypereosinophilic syndrome encompasses a diverse group of blood disorders characterized by persistent, unexplained hypereosinophilia leading to tissue damage. Cardiac involvement occurs in around 20% of cases of hypereosinophilic syndrome and marks a critical phase. Our report highlights the importance of considering eosinophilic myocarditis and SHI when evaluating patients with chest pain and hypereosinophilia. It emphasizes the subtleties of diagnosis and the imperative of early identification and appropriate treatment to improve prognosis in cases of eosinophilic myocarditis. This case highlights the diverse clinical manifestations of myocarditis and the essential need for a comprehensive diagnostic approach in the presence of chest pain and hypereosinophilia.
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