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A case report of arrhythmogenic ventricular cardiomyopathy presenting with sustained ventricular tachycardia arising from the right and the left ventricles before structural changes are documented

机译:记录有心律失常性室性心肌病伴有持续性室性心动过速由右心室和左心室引起在记录结构改变之前

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摘要

Arrhythmogenic ventricular cardiomyopathy (AC) is a genetic progressive disease characterized by fibro-fatty replacement of either ventricles in isolation or in combination. Arrhythmogenic ventricular cardiomyopathy is frequently associated with ventricular tachycardia (VT) having a left bundle branch block (LBBB) morphology and much more rarely with VT having right bundle branch block (RBBB) morphology even when the left ventricle is involved. Cardiac magnetic resonance (CMR) imaging plays a key role in the diagnosis of AC. Sustained VT in AC may occur in the concealed stage of the disease before the manifestation of morphological abnormalities on echocardiogram; however, they almost always are accompanied by structural abnormalities of the ventricles on CMR.
机译:心律失常性心室心肌病(AC)是一种遗传性进行性疾病,其特征是孤立或联合使用心室纤维脂肪替代。心律失常性室性心肌病通常与具有左束支传导阻滞(LBBB)形态的室性心动过速(VT)相关,很少发生具有右束支传导阻滞(RBBB)形态的室速,即使累及左心室也是如此。心脏磁共振(CMR)成像在AC诊断中起关键作用。在超声心动图上形态异常出现之前,AC的持续VT可能发生在疾病的隐蔽阶段。然而,它们几乎总是伴随着CMR的心室结构异常。

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