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先天性异常/迷走体循环动脉至肺静脉瘘:血管封堵器及弹簧圈栓塞术闭合瘘口

Congenital anomalous/aberrant systemic artery to pulmonary venous fistula: closure with vascular plugs & coil embolization.

作者信息

Jariwala Pankaj, Ramesh G, Sarat Chandra K

机构信息

Indo-US Superspeciality Hospitals, Shyam Karan Road, Anand Bagh, Ameerpet, Andhra Pradesh 500016, India.

Nizam's Institute of Medical Science, Punjagutta, Andhra Pradesh 500082, India.

出版信息

Indian Heart J. 2014 Jan-Feb;66(1):95-103. doi: 10.1016/j.ihj.2013.10.009.

Abstract

A 7-month-old girl with failure to thrive, who, on clinical and diagnostic evaluation [echocardiography & CT angiography] to rule out congenital heart disease, revealed a rare vascular anomaly called systemic artery to pulmonary venous fistula. In our case, there was dual abnormal supply to the entire left lung as(1) anomalous supply by normal systemic artery internal mammary artery and an aberrant feeder vessel from the abdominal aorta. Left Lung had normal bronchial connections and normal pulmonary vasculature. The fistula drained through the pulmonary veins to the left atrium leading to 'left-left shunt'. Percutaneous intervention in two stages was performed using Amplatzer vascular plugs and coil embolization to close them successfully. The patient gained significant weight in follow up with other normal developmental and mental milestones.

摘要

一名7个月大的发育迟缓女童,在进行临床和诊断评估[超声心动图和CT血管造影]以排除先天性心脏病时,发现了一种罕见的血管异常,称为体动脉至肺静脉瘘。在我们的病例中,整个左肺存在双重异常供血,即(1)由正常体动脉[胸廓内动脉]进行的异常供血,以及(2)来自腹主动脉的一支异常供血血管。左肺的支气管连接和肺血管系统正常。瘘管通过肺静脉引流至左心房,导致“左向左分流”。分两个阶段进行了经皮介入治疗,使用Amplatzer血管封堵器和弹簧圈栓塞成功地封闭了瘘管。在随访中,患者体重显著增加,同时其他发育和智力指标均正常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a170/4054825/d52f7abd3903/gr1.jpg

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