Can Multi-Detector Computed Tomography Classify (MDCT) Non-Compacted Left Ventricle in Coloration to The Genetic Structure?

M. Nabo
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Abstract

Introduction Isolated left ventricular noncompaction (LVNC) is a genetic cardiomyopathy characterized by prominent ventricular trabeculations and deep intertrabecular recesses, or sinusoids, in communication with the left ventricular cavity [1]. The clinical sequelae of these deformities are the syndrome of heart failure, arrhythmias and stroke. Dusek first described the postnatal persistence of spongy myocardium in 1975 pathologically, but Engberding and Bender made the first clinical recognition with two-dimensional (2D) echocardiography in 1984 [2,3]. Three decades later, with only morphologic assessment available and no definitive genetic pathway, isolated left ventricular noncompaction (LVNC) remains a diagnostic and management challenge. In this review, we wish to spot light on how MDCT can visualize the shape and distribution of spongy myocardium clearer than echocardiography.
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多检测器计算机断层扫描(MDCT)是否可以根据遗传结构对非压缩左心室进行分类?
孤立性左室不压实(LVNC)是一种遗传性心肌病,其特征是突出的心室小梁和与左室腔相通的深小梁间窝或窦状窝[1]。这些畸形的临床后遗症是心力衰竭、心律失常和中风的综合征。Dusek于1975年首次在病理学上描述了海绵状心肌在出生后的持续存在,Engberding和Bender于1984年通过二维超声心动图首次在临床中发现[2,3]。三十年后,由于只有形态学评估,没有明确的遗传途径,孤立性左室非压实(LVNC)仍然是诊断和治疗的挑战。在这篇综述中,我们希望阐明MDCT如何比超声心动图更清晰地显示海绵状心肌的形状和分布。
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