Karmegaraj Balaganesh, Vijayakumar Sowmya
Amrita institute of Medical Sciences and research centre, Kochi, Kerala, India.
Sowmi Pediatric Heart Centre, B83/1, 1st main road, Maharaja Nagar, Tirunelveli, Tamilnadu, 627002, India.
Pediatr Radiol. 2025 Aug 18. doi: 10.1007/s00247-025-06367-3.
Advances in fetal echocardiography, including conventional 2-dimensional (D) and 3-D/4-D imaging techniques, have improved our understanding of upper mediastinal vessels.
To study the prenatal imaging characteristics, pregnancy, and postnatal outcomes in fetuses with an isolated anomalous course of the left brachiocephalic vein.
This retrospective study, conducted between October 2019 and July 2024, examined fetuses with an isolated anomalous course of the left brachiocephalic vein. These cases underwent conventional 2-D and 3-D/4-D spatiotemporal image correlation echocardiography at Sowmi Pediatric Heart Centre, Tirunelveli, India. The inclusion criteria encompassed all fetuses with an isolated anomalous course of the left brachiocephalic vein, whereas those with associated congenital heart defects or missing postnatal follow-up were excluded from the analysis.
A total of 2,083 fetal echocardiograms were performed during the study period. In total, 331 fetal cardiac abnormalities were detected. Twelve fetuses with isolated anomalous course of left brachiocephalic vein were included in the study. Intrathymic left brachiocephalic vein was observed in nine fetuses, extrathymic left brachiocephalic vein in two fetuses, and retroaortic left brachiocephalic vein in one fetus. Quadruple marker screening in five cases yielded normal results. Invasive genetic testing performed in the case with retroaortic left brachiocephalic vein showed normal findings. Postnatally, no dysmorphism was observed in any fetus. All fetuses were delivered at term, had an uneventful postnatal period, underwent at least 3 months of follow-up, and were reassured.
Though the indication for referral for this fetal extracardiac anomaly was to rule out critical congenital heart disease, proper prenatal imaging of this benign finding will avoid unnecessary confusion, in utero referral to tertiary pediatric heart center for delivery and invasive genetic tests.
胎儿超声心动图的进展,包括传统二维(2D)和三维/四维成像技术,增进了我们对纵隔上部血管的了解。
研究孤立性左头臂静脉走行异常胎儿的产前影像特征、妊娠情况及产后结局。
这项回顾性研究于2019年10月至2024年7月进行,纳入孤立性左头臂静脉走行异常的胎儿。这些病例在印度蒂鲁内尔维利的索米儿科心脏中心接受了传统二维和三维/四维时空图像相关超声心动图检查。纳入标准包括所有孤立性左头臂静脉走行异常的胎儿,而伴有先天性心脏缺陷或产后失访的胎儿被排除在分析之外。
研究期间共进行了2083次胎儿超声心动图检查。总共检测到331例胎儿心脏异常。12例孤立性左头臂静脉走行异常的胎儿被纳入研究。9例胎儿观察到胸腺内左头臂静脉,2例胎儿观察到胸腺外左头臂静脉,1例胎儿观察到主动脉后左头臂静脉。5例病例的四联筛查结果正常。对主动脉后左头臂静脉病例进行的侵入性基因检测结果正常。产后,所有胎儿均未观察到畸形。所有胎儿均足月分娩,产后情况平稳,至少接受了3个月的随访,结果令人放心。
尽管转诊进行这种胎儿心外异常检查的目的是排除严重先天性心脏病,但对这一良性发现进行适当的产前成像将避免不必要的混淆、宫内转诊至三级儿科心脏中心分娩以及侵入性基因检测。