首页> 外文期刊>Journal of Ultrasound in Medicine: Official Journal of the American Institute of Ultrasound in Medicine >Prenatal Diagnosis of Ventriculocoronary Arterial Communication in Fetuses With Hypoplastic Left Heart Syndrome
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Prenatal Diagnosis of Ventriculocoronary Arterial Communication in Fetuses With Hypoplastic Left Heart Syndrome

机译:发育不良的左心综合征胎儿的心室冠状动脉通信的产前诊断。

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Objective. The purpose of this series was to describe the fetal echocardiographic findings in hypoplastic left heart syndrome with aortic atresia and ventriculocoronary arterial communication and implications of these findings. Methods. We describe 2 fetuses with hypoplastic left heart syndrome with ventriculocoronary arterial communication diagnosed at 29 and 20 weeks' gestation, respectively. The underlying cardiac anatomy consisted of a hypoplastic left heart and mitral stenosis with aortic atresia. We used color Doppler and pulsed Doppler sonography on the surface of the myocardium to specifically look for coronary arterial flow. Results. By color Doppler sonography, ventriculocoronary arterial communication was shown between the left ventricular cavity and the left coronary artery with characteristic bidirectional flow on pulsed Doppler examination. There was no mitral regurgitation. The left ventricular myocardium was substantially hypertrophied. The first patient underwent surgical Norwood palliation and died after a prolonged postoperative course. The second patient underwent stenting of the arterial duct and bilateral pulmonary artery banding in the catheterization laboratory but died after a few weeks. Implications of ventriculocoronary arterial communication in association with hypoplastic left heart syndrome are discussed. Conclusions. It is possible to accurately diagnose ventriculocoronary arterial communication on fetal echocardiography. The presence of ventriculocoronary arterial communication is seen exclusively in a subgroup of patients with an aortic atresia and mitral stenosis variant of hypoplastic left heart syndrome. The prognosis is poor in this subgroup of patients.
机译:目的。本系列的目的是描述胎儿超声心动图检查发现的增生性左心综合征伴主动脉闭锁和心室冠状动脉的通信以及这些发现的意义。方法。我们描述了2名胎儿,分别在妊娠29和20周被诊断出患有左心发育不全综合征,并通过房室动脉通信进行了诊断。潜在的心脏解剖结构包括发育不良的左心和二尖瓣狭窄伴主动脉闭锁。我们在心肌表面上使用了彩色多普勒和脉冲多普勒超声检查,以专门寻找冠状动脉血流。结果。通过彩色多普勒超声检查,在脉冲多普勒检查中显示出左心室腔与左冠状动脉之间的心室动脉连通,并具有特征性双向流动。没有二尖瓣反流。左心室心肌明显肥大。首例患者接受了诺伍德手术治疗,并在延长的术后过程中死亡。第二例患者在导管实验室接受了动脉导管支架置入术和双侧肺动脉束带术,但几周后死亡。讨论了室性肺动脉通信与发育不良性左心综合征的关联。结论。可以通过胎儿超声心动图准确诊断心室冠状动脉通信。仅在亚组中存在增生性左心综合征的主动脉闭锁和二尖瓣狭窄变异的患者亚组中才能看到房室和肺动脉的通信。该亚组患者的预后较差。

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