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产前超声心动图诊断双侧动脉导管未闭与心血管畸形的新组合:一例报告及文献综述

Prenatal echocardiography diagnosis of a novel combination of bilateral ductus arteriosus and cardiovascular anomalies: a case report and literature review.

作者信息

Zhang Simin, Wang Ning, Qu Pengfei, Shu Xiaobin, Mi Yang, Gao Xinru

机构信息

Ultrasonic Diagnosis Center, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China.

Translational Medicine Center, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China.

出版信息

Front Cardiovasc Med. 2024 May 9;11:1389759. doi: 10.3389/fcvm.2024.1389759. eCollection 2024.

Abstract

BACKGROUND

Bilateral ductus arteriosus (BDA) is a relatively rare vascular malformation. According to the double arch theory, BDA is formed when the distal ends of the sixth pairs of primitive arches on the left and right sides have not regressed. We describe a fetus with prenatal echocardiographic findings of BDA and right aortic arch mirror-image branching (RAA-MIB) combined with congenital heart disease. Furthermore, to gain a deeper understanding of the embryological mechanism of BDA, we review the literature on all combinations of BDA present in 40 fetuses/infants.

CASE SUMMARY

A 22-year-old female patient underwent fetal echocardiography at 23 weeks of gestation. Both the two-dimensional (2D) grayscale image and color Doppler flow imaging (CDFI) revealed dextro-transposition of the great arteries combined with a ventricular septal defect and RAA-MIB. The following scan revealed a rare vascular ring, which was identified as BDA extending from the confluent of the left pulmonary artery and right pulmonary artery, completely encircling the trachea to form an "O"-shaped vascular ring before finally converging into the descending aorta. A persistent left superior vena cava was also observed. We subsequently used four-dimensional (4D) color Doppler imaging with the spatiotemporal image correlation (STIC) HD live flow and STIC HD live flow silhouette mode to clearly display ventricular arterial connectivity and the direction of vessel travel. Adjusting the image quality and display angle is very important when applying STIC. The 4D images confirmed our diagnosis. After multidisciplinary counseling and discussion with her family, this female patient decided to terminate the pregnancy.

CONCLUSION

Our review of the literature summarized nine combinations classified into three types of BDA and aortic arch pathology. However, our case differs because it is a novel combination of intracardiac structural abnormalities and vascular rings in a fetus. Prenatal ultrasound diagnosis of BDA is important and requires a combination of 2D grayscale, CDFI, and STIC images to assist in scanning.

摘要

背景

双侧动脉导管(BDA)是一种相对罕见的血管畸形。根据双弓理论,当左右两侧第六对原始弓的远端未退化时,就会形成BDA。我们描述了一名胎儿,其产前超声心动图检查发现有BDA和右位主动脉弓镜像分支(RAA-MIB)并伴有先天性心脏病。此外,为了更深入地了解BDA的胚胎学机制,我们回顾了40例胎儿/婴儿中出现的BDA所有组合的相关文献。

病例摘要

一名22岁女性患者在妊娠23周时接受了胎儿超声心动图检查。二维(2D)灰阶图像和彩色多普勒血流成像(CDFI)均显示大动脉右旋位合并室间隔缺损和RAA-MIB。随后的扫描发现了一个罕见的血管环,经确认是从左肺动脉和右肺动脉汇合处延伸出的BDA,它完全环绕气管形成一个“O”形血管环,最终汇入降主动脉。还观察到一条永存左上腔静脉。随后我们使用了具有时空图像相关(STIC)高清实时血流和STIC高清实时血流轮廓模式的四维(4D)彩色多普勒成像,以清晰显示心室动脉连接情况和血管走行方向。应用STIC时调整图像质量和显示角度非常重要。4D图像证实了我们的诊断。在与家人进行多学科咨询和讨论后,这名女性患者决定终止妊娠。

结论

我们对文献的回顾总结了九种组合,分为三种类型的BDA和主动脉弓病变。然而,我们的病例有所不同,因为它是胎儿中心内结构异常和血管环的一种新组合。产前超声诊断BDA很重要,需要结合2D灰阶、CDFI和STIC图像来辅助扫描。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fda/11111948/7a15016fa5a2/fcvm-11-1389759-g001.jpg

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