胎儿右心室外翻与心室双裂有关

A. Benatar, A. Vorsselmans
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引用次数: 0

摘要

先天性右心室憩室是一种在心室自由壁内的跨壁局部突出物。这些憩室在胎儿时期很少被诊断出来,由于它们的罕见性,它们的自然历史仍然不清楚。我们提出的情况下,产前诊断的右心室憩室在妊娠26周与心室重音节律不规则相关。病例报告我们提出一个病例32岁的G1P1,谁是在妊娠26周,由于心律异常和四腔视图的常规筛查。胎儿超声心动图显示一个大的右心室流出(RVO),大小为11 × 9 mm,血流不受限制,穿过一个大孔,位于三尖瓣下方的外侧自由壁。结论胎儿RVO是一种罕见的先天性畸形,在常规四腔镜下发现额外的腔时,在评估胎儿心律失常或存在心包积液时需要考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Foetal right ventricular outpouching associated with ventricular bigeminy
Introduction Congenital cardiac right ventricular diverticula are transmural localised protrusions, within the free wall of the ventricles. These diverticula are infrequently diagnosed during the foetal period, and because of their rarity, their natural history remains unclear. We present a case of a prenatal diagnosis of right ventricular diverticulum at 26 weeks gestation associated with an irregular rhythm of ventricular bigeminy. Case report We present a case of a 32-yearold G1P1, who was referred at 26 weeks gestation on account of an abnormal rhythm and four-chamber view on a routine screening. Foetal echocardiography showed a large right ventricular outpouching (RVO) of 11 × 9 mm, with unrestricted flow, across a large orifice and situated along the lateral free wall, just beneath the tricuspid valve. Conclusion Foetal RVO are rare congenital malformations that need to be considered, when an extra chamber is visualised in the routine four-chamber view, in the assessment of foetal arrhythmia or presence of a pericardial effusion.
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