Retroesophageal Left Brachiocephalic Vein with Right-Sided Aortic Arch in Tetralogy of Fallot: A Rare Venous Anomaly Demonstrated on Computed Tomography Angiography.

Q2 Medicine Methodist DeBakey cardiovascular journal Pub Date : 2024-11-05 eCollection Date: 2024-01-01 DOI:10.14797/mdcvj.1424
Archita Mahajan, Mansi Verma, Sushma Makhaik
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Abstract

A 14-year-old child with recurrent cyanotic spells at the age of 9 months underwent echocardiography at that time, which revealed tetralogy of Fallot (TOF). Follow-up computed tomography angiography revealed TOF with valvular pulmonary stenosis and a right-sided aortic arch with mirror image branching. Interestingly, an unusual anomalous course of the left brachiocephalic vein was seen. Instead of coursing anterior to the aortic arch, the left brachiocephalic vein had a U-shaped course like a garland, where it descended vertically down behind the esophagus and the descending aorta, crossed the midline at T4 level of the vertebral body, and then ascended upwards to join the superior vena cava. This case highlights the role of computed angiography in depicting anomalous venous anatomy in TOF, which can have potential clinical implications.

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法洛氏四联症食管后左侧肱静脉伴右侧主动脉弓:计算机断层扫描血管造影显示的罕见静脉异常。
一名 14 岁患儿在 9 个月大时反复出现发绀症状,当时接受了超声心动图检查,结果显示患儿患有法洛氏四联症(TOF)。随访的计算机断层扫描血管造影显示,TOF伴有瓣膜性肺动脉狭窄和右侧主动脉弓镜像分支。有趣的是,左侧肱脑静脉的走向异常。左侧肱静脉没有在主动脉弓前方走行,而是像花环一样呈 U 型走行,在食管和降主动脉后方垂直向下,在椎体 T4 水平处穿过中线,然后向上与上腔静脉汇合。该病例凸显了计算机血管造影在描述 TOF 异常静脉解剖结构方面的作用,这可能会产生潜在的临床影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.30
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发文量
65
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