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

机译:先天性异常/异常系统性动脉至肺静脉瘘:用血管栓塞和线圈栓塞术封闭

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摘要

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 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.
机译:一名7个月大的女孩未能to壮成长,她通过临床和诊断评估[超声心动图和CT血管造影]排除了先天性心脏病,发现了一种罕见的血管异常,称为系统性动脉至肺静脉瘘。在我们的案例中,由于正常的全身动脉[内乳动脉]和腹主动脉的异常供体血管的异常供应,整个左肺都有双重异常供应。左肺支气管连接正常,肺血管正常。瘘管经肺静脉排至左心房,导致“左-左分流”。使用Amplatzer血管栓塞和线圈栓塞术成功分两个阶段进行经皮介入。在随访其他正常的发育和精神里程碑时,患者体重显着增加。

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