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患有复杂先天性心脏病的新生儿的右心室心肌致密化不全

Right ventricular noncompaction in a neonate with complex congenital heart disease.

作者信息

Alehan Dursun, Dogan Omer Faruk

机构信息

Division of Pediatric Cardiology, Hacettepe University Faculty of Medicine, Sihhiye, Ankara, Turkey.

出版信息

Cardiol Young. 2005 Aug;15(4):434-6. doi: 10.1017/S1047951105000910.

DOI:10.1017/S1047951105000910
PMID:16014196
Abstract

Ventricular noncompaction is a rare unclassified cardiomyopathy occurring because of arrest of the normal intrauterine compaction of the loose luminal component of the ventricular myocardium. There is limited data regarding its diagnosis and outcome in children. It is recognised, however, that right ventricular involvement is extremely rare. We report a case in which only the right ventricular myocardium was noncompacted, a situation which led to heart failure soon after birth.

摘要

心室致密化不全是一种罕见的未分类心肌病,由于胎儿期心室心肌疏松腔内容物正常致密化过程停滞所致。关于其在儿童中的诊断和预后的数据有限。然而,人们认识到右心室受累极为罕见。我们报告一例仅右心室心肌致密化不全的病例,这种情况在出生后不久即导致心力衰竭。

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Noncompaction of Ventricular Myocardium Involving the Right Ventricle.累及右心室的心室心肌致密化不全
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Right ventricular morphology and systolic function in left ventricular noncompaction cardiomyopathy.左心室致密化不全性心肌病的右心室形态和收缩功能。
Am J Cardiol. 2014 Mar 15;113(6):1018-23. doi: 10.1016/j.amjcard.2013.12.008. Epub 2013 Dec 25.
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Isolated right ventricular noncompaction in a newborn.新生儿孤立性右心室心肌致密化不全
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Biventricular noncompaction in a patient with dextrocardia/dextroversion diagnosed with cardiac magnetic resonance imaging.经心脏磁共振成像诊断为右位心/右心室转位患者的双心室心肌致密化不全。
Can J Cardiol. 2009 Sep;25(9):e335-6. doi: 10.1016/s0828-282x(09)70151-5.
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Unusual association between "congenitally corrected transposition of the great arteries" and "noncompaction" of the right systemic ventricle.“先天性矫正型大动脉转位”与右心室“心肌致密化不全”之间的罕见关联。
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