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All That Glitters is not Gold: Apical Hypertrophic Cardiomyopathy Mimicking Acute Coronary Syndrome

机译:所有闪闪发光的东西都不是金子:模仿急性冠状动脉综合征的根尖肥厚型心肌病

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摘要

Hypertrophic cardiomyopathy is characterized by the idiopathic hypertrophy of the left ventricle (and occasionally right ventricle). HCM is an autosomal dominant disease, with variable penetration. In Asian population, apical hypertrophic cardiomyopathy is relatively common (25%). However, this is relatively rare in Caucasian population (0.2%). Patients with HCM, often presents with typical exertional chest pain and shortness of breath. Apical HCM patients tend to have milder symptoms. However, the clinical presentation and electrocardiographic features of Apical HCM often mimic acute coronary syndrome and high index of suspicion is warranted in differentiating this condition. Patients with apical HCM have relatively better prognosis when compare to the other varieties. Here, we are presenting a patient who presented with typical exertional chest pain whose electrocardiographic changes are concerning for acute ischemic changes.
机译:肥厚型心肌病的特征是左心室(有时是右心室)的特发性肥大。 HCM是常染色体显性疾病,具有可变的渗透性。在亚洲人群中,根尖肥厚型心肌病相对常见(25%)。然而,这在白人人群中相对较少(0.2%)。 HCM患者经常表现出典型的劳累性胸痛和呼吸急促。顶端HCM患者倾向于有较轻的症状。然而,心尖部HCM的临床表现和心电图特征通常模仿急性冠状动脉综合征,因此在区分这种情况时应高度怀疑。与其他品种相比,顶端HCM患者的预后相对较好。在这里,我们向患者介绍典型的劳累性胸痛,其心电图改变与急性缺血性改变有关。

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