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Oesophageal atresia and tracheoesophageal fistula with right pulmonary agenesis and duplication of the azygos vein

机译:食管闭锁和气管食管瘘合并右肺发育不全和奇静脉重复

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A premature (35 weeks' gestation) girl developed respiratory-distress immediately after birth along with frothing from the mouth. A nasogastric tube could not be passed. Breath sounds were absent on the right side of the chest and the cardiac apex beat was located on the right side. Chest x-ray revealed opacification of the right hemithorax, absence of the right lung shadow, apparent dextrocardia and a hyperaerated left lung crossing the midline (figure 1). The upper oesophagus with the feeding tube coiled in it was deviated to the right. Thoracotomy revealed absence of the right lung, two azy-gos veins adjacent to each other, each with three tributaries (figure 2), and a right-sided aortic arch. The patient had oesoph-ageal atresia (OA) with distal tracheoesophageal fistula (TEF) which was repaired. The baby died on the third postoperative day from progressive respiratory failure.
机译:一名早产(妊娠35周)的女孩出生后立即出现呼吸窘迫,并从嘴里冒出泡沫。鼻胃管无法通过。胸部右侧没有呼吸音,右侧心跳位于右侧。胸部X线片显示右半胸椎浑浊,无右肺阴影,明显的心动过速和左中气横穿中线(图1)。食管盘绕的上段食管向右偏斜。胸廓切开术显示右肺不存在,两条彼此相邻的azy-gos静脉,每条具有三个支流(图2)和右侧主动脉弓。患者患有食管-胃闭锁(OA),并修补了远端气管食管瘘(TEF)。婴儿在术后第三天因进行性呼吸衰竭死亡。

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