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Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature

机译:发育不良左心综合征的主动脉瓣缺失而产前诊断和成功缓解:一例报道并文献复习

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摘要

>Introduction  Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS). >Case  A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypoplastic left atrium, nearly atretic mitral valve, small left ventricle, and a hypoplastic aortic valve with severe aortic insufficiency. A female infant was born at term and postnatal ECHO confirmed the above findings. In addition, there was complete absence of the aortic valve leaflets. The patient underwent Norwood's procedure at day 5 of life with atrial septectomy, over-sewing of the aortic valve annulus, and a 4 mm Sano's shunt between the right ventricle and the main pulmonary artery. She tolerated this surgery well and subsequently underwent a bidirectional Glenn's procedure at 8 months of life. >Conclusion  Prenatal diagnosis of absent aortic valve should be suspected in the presence of severe aortic insufficiency in the fetal ECHO. Early postnatal intervention is critical as those patients are likely to deteriorate quickly. The over-sewing of the aortic valve may be important to prevent coronary steal and myocardial hypoperfusion which could potentially be detrimental.
机译:>简介先天性主动脉瓣小叶缺失与左心发育不全综合征(HLHS)少见。 >病例一名37岁的孕妇在妊娠22周时接受了胎儿胎儿可能的HLHS评估。胎儿超声心动图(ECHO)表现为左心房发育不良,二尖瓣近乎闭锁,左心室较小以及主动脉瓣关闭不全的主动脉瓣发育不良。一名女婴在足月出生,产后回声证实了上述发现。另外,完全没有主动脉瓣小叶。该患者在生命的第5天接受了Norwood手术,进行了房间隔切除术,主动脉瓣环缝合过度以及右心室和肺主动脉之间的4mm萨诺(Sano)分流。她很好地耐受了该手术,随后在生命的8个月内接受了双向Glenn手术。 >结论 in如果胎儿的ECHO存在严重的主动脉瓣关闭不全,则应怀疑产前诊断为主动脉瓣缺失。产后早期干预至关重要,因为这些患者可能会迅速恶化。主动脉瓣的过度缝合对于防止可能有害的冠状动脉窃取和心肌灌注不足可能很重要。

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