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孤立性左心室心肌致密化不全合并胎儿因病态窦房结综合征导致的持续性心动过缓。

Isolated noncompaction of left ventricular myocardium with fetal sustained bradycardia due to sick sinus syndrome.

作者信息

Ozkutlu Süheyla, Onderoglu Lütfü, Karagöz Tevfik, Celiker Alpay, Sahiner Umit Murat

机构信息

Section of Cardiology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 2006 Oct-Dec;48(4):383-6.

Abstract

Noncompaction of the ventricular myocardium is a rare congenital cardiomyopathy resulting from an arrest in normal endomyocardial embryogenesis. This disease is characterized by numerous and prominent trabeculations and deep intertrabecular recesses. It may be isolated or associated with other congenital heart diseases. The disorder is clinically accompanied by depressed ventricular function, systemic embolization and arrhythmias. Sustained bradycardia is infrequent in prenatal life and associated with maternal collagen vascular diseases, structural heart diseases or long QT syndrome. Herein we report a case of isolated noncompaction of left ventricular myocardium diagnosed in the first day of life and followed previously by serial fetal echocardiograms for the sustained sinus bradycardia. On postnatal electrocardiography, there was junctional escape rhythm due to profound sinus bradycardia, leading us to consider sick sinus syndrome. To our knowledge, this is the first case in the literature of isolated noncompaction of left ventricular myocardium with sustained bradycardia due to sick sinus syndrome.

摘要

心室心肌致密化不全是一种罕见的先天性心肌病,由正常心内膜胚胎发育停滞所致。该病的特征是有许多明显的肌小梁和深陷的小梁间隐窝。它可以是孤立性的,也可与其他先天性心脏病相关。该疾病临床上伴有心室功能减退、全身性栓塞和心律失常。持续性心动过缓在产前并不常见,且与母体胶原血管疾病、结构性心脏病或长QT综合征有关。在此,我们报告一例出生第一天诊断为孤立性左心室心肌致密化不全的病例,产前曾因持续性窦性心动过缓接受系列胎儿超声心动图检查。出生后心电图显示,由于严重窦性心动过缓出现交界性逸搏心律,使我们考虑病态窦房结综合征。据我们所知,这是文献中首例因病态窦房结综合征导致持续性心动过缓的孤立性左心室心肌致密化不全病例。

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