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产前诊断下腔静脉肝段缺如伴奇静脉/半奇静脉延续:病例系列。

Prenatal diagnosis of hepatic interruption of the inferior vena cava with azygos/hemiazygos continuation without structural heart defects: A case series.

机构信息

Department of Pediatric Cardiology, Kocaeli University School of Medicine, Kocaeli, Turkey.

Department of Perinatology, Kocaeli University School of Medicine, Kocaeli, Turkey.

出版信息

J Clin Ultrasound. 2022 Jul;50(6):795-802. doi: 10.1002/jcu.23209. Epub 2022 Mar 30.

DOI:10.1002/jcu.23209
PMID:35355279
Abstract

OBJECTIVES

To describe fetal spectrum and echocardiographic characteristics of interrupted inferior vena cava (IIVC) with azygos/hemiazygous continuation without other structural heart defects and to evaluate its association with visceral heterotaxy and isomerism, extracardiac and genetic anomalies, and to review neonatal outcome.

METHODS

This was a retrospective study of 14 fetuses with a confirmed diagnosis of IIVC with normal intracardiac anatomy. The following variables were collected; indication for referral, gestational age at diagnosis; associated isomerism and visceral heterotaxy, heart rhythm, genetic and extracardiac abnormalities, and fetal/neonatal outcome.

RESULTS

Among 36 fetuses with IIVC, 14 cases (38.8%) had normal intracardiac anatomy. These IIVC cases correspond to 0.19% (14/7250) of all fetal cardiac examinations, and to 1.5% (14/922) of all cardiac abnormalities. Six patients had visceral abnormalities. Atrial appendage morphology was clearly depicted in three fetuses, both appendages were left. One fetus had bradyarrhythmia revealing atrial ectopic rhythm. Six fetuses did not have any concomitant cardiac or visceral abnormalities, therefore regarded as isolated. All babies were delivered at term with a good prognosis.

CONCLUSION

Our study has shown that almost half of the IIVC cases without intracardiac structural anomalies displayed other findings of isomerism while the other half was isolated benign vascular variant. Therefore, prenatal diagnosis of IIVC should prompt a comprehensive evaluation for cardiac, situs, and visceral anomalies. The outcome is favorable.

摘要

目的

描述下腔静脉中断(IVVC)伴奇静脉/半奇静脉连续性,无其他结构性心脏缺陷的胎儿频谱和超声心动图特征,并评估其与内脏异构和同形同构、心脏外和遗传异常的关系,并回顾新生儿结局。

方法

这是一项对 14 例经证实存在 IVVC 且伴有正常心内解剖结构的胎儿的回顾性研究。收集了以下变量:转诊指征、诊断时的孕龄;伴同异构和内脏异构、心律、遗传和心脏外异常、胎儿/新生儿结局。

结果

在 36 例 IVVC 胎儿中,14 例(38.8%)存在正常心内解剖结构。这些 IVVC 病例占所有胎儿心脏检查的 0.19%(14/7250),占所有心脏异常的 1.5%(14/922)。6 例患者存在内脏异常。3 例胎儿的心房附件形态清晰,均为左心房附件。1 例胎儿出现心动过缓,显示房性异位节律。6 例胎儿无任何心脏或内脏异常,因此被视为孤立性。所有婴儿均足月分娩,预后良好。

结论

我们的研究表明,几乎一半的 IVVC 病例无心内结构异常,显示出异构的其他表现,而另一半是孤立的良性血管变异。因此,IVVC 的产前诊断应提示全面评估心脏、 situs 和内脏异常。结局是良好的。

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