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首页> 外文期刊>Echocardiography. >The evolution of apical hypertrophic cardiomyopathy: Development of mid‐ventricular obstruction and apical aneurysm 11?years after initial diagnosis
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The evolution of apical hypertrophic cardiomyopathy: Development of mid‐ventricular obstruction and apical aneurysm 11?years after initial diagnosis

机译:Abiscic肥厚性心肌病的演变:中心室梗阻的发展和顶端动脉瘤11?初步诊断后数年

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摘要

Asian hypertrophic cardiomyopathy ( AHCM ) is a rare variant of hypertrophic cardiomyopathy ( HCM ) that is more prevalent in the Asian population. There is significant overlap between AHCM , mid‐cavitary obstruction, and apical aneurysms. Although more benign compared to HCM , the course of AHCM is not clearly defined. We present an interesting case of an African American male with known AHCM who develops symptomatic mid‐cavitary obstruction and apical aneurysm 11?years after initial diagnosis.
机译:亚洲肥厚性心肌病(AHCM)是亚洲人口中较为普遍的肥厚性心肌病(HCM)的罕见变体。 AHCM,中间空间阻塞和顶端动脉瘤之间存在显着重叠。 虽然与HCM相比更良好,但没有明确定义AHCM的过程。 我们向非洲裔美国男性发挥了一个有趣的案例,其中已知的AHCM在初步诊断后发育症状中间腔内梗阻和顶端动脉瘤11年。

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