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[46日龄婴儿肺动脉吊带的手术修复]

[Surgical repair for pulmonary artery sling on a 46-day-old infant].

作者信息

Horikoshi J, Takanashi Y, Tokuhiro K, Yoshiwara K, Koyama N, Komatsu H

机构信息

Department of Thoracic Cardiovascular Surgery, Toho University, School of Medicine, Tokyo, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1990 Aug;38(8):1321-5.

PMID:2230388
Abstract

Surgical repair on a 46-day-old girl with pulmonary artery sling is reported. She was suffered from dypnea and admitted to a hospital on 12 days after her birth. On chest roentgenogram atelectasis of right lung was found. She had been on respirator since 21 days after her birth. On bronchogram and pulmonary arteriogram, the trachea and right bronchus were compressed and shifted with the anomalous origin of left pulmonary artery which originated from the right pulmonary artery and passed between the trachea and esophagus. These results confirmed the diagnosis of pulmonary artery sling. Hence, she was referred to our hospital for surgical treatment. She underwent surgical repair on 46-day-old. In operation, we chose a mid-sternal splitting incision, and excised 5 mm of ductus arteriosus. Under extracorporeal circulation, the left pulmonary artery was amptated from the right pulmonary artery and pulled back to left side between the trachea and the esophagus. The left pulmonary artery was anastomosed to the main pulmonary artery at the anterior to the left bronchus. She weaned from respirator, and was extubated on the 3rd day after procedure. She recovered uneventfully in post-operative course. On the 24th day after operation she discharged from hospital. On pulmonary perfusion scanning and pulmonary arteriography performed one year after operation, the left pulmonary artery was patient with slightly decreased perfusion in the left lung. Surgical repair for pulmonary artery sling was recognized as high mortality because of frequently associated tracheobronchial anomalies. In the Japanese literature, only 4 patients survived surgically and lived in late stage.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报道了一例对46日龄患有肺动脉吊带的女孩进行手术修复的病例。她出生后12天因呼吸困难入院。胸部X线片显示右肺肺不张。她自出生后21天起就一直使用呼吸机。支气管造影和肺动脉造影显示,气管和右支气管受压并移位,左肺动脉起源异常,起自右肺动脉并在气管和食管之间穿行。这些结果证实了肺动脉吊带的诊断。因此,她被转诊至我院接受手术治疗。她在46日龄时接受了手术修复。手术中,我们选择胸骨正中劈开切口,切除了5毫米的动脉导管。在体外循环下,将左肺动脉从右肺动脉离断并拉回到气管和食管之间的左侧。将左肺动脉与左主支气管前方的主肺动脉进行吻合。术后第3天她脱离呼吸机并拔除气管插管。术后恢复顺利。术后第24天她出院。术后一年进行的肺灌注扫描和肺动脉造影显示,左肺动脉灌注稍减少。由于常伴有气管支气管畸形,肺动脉吊带的手术修复被认为死亡率较高。在日本文献中,仅有4例手术存活并活到后期。(摘要截短至250字)

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