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右旋心、左肺动脉吊带和气管狭窄患者行滑式气管成形术后发生主动脉-气管瘘:1 例报告。

Aortotracheal fistula after slide tracheoplasty in a patient with dextrocardia, left pulmonary artery sling and tracheal stenosis: a case report.

机构信息

Department of Critical Care Mackay Memorial Hospital, CVICU-B, 7F, No. 92, Sec. 2, Zhongshan N. Rd, Taipei City, Taiwan.

Department of Pediatric Cardiology Mackay Children's Hospital, PICU, 11F, No. 92, Sec. 2, Zhongshan N. Rd, Taipei City, Taiwan.

出版信息

J Cardiothorac Surg. 2021 Mar 31;16(1):62. doi: 10.1186/s13019-021-01438-6.

Abstract

BACKGROUND

Aortotracheal fistula (ATF) is an uncommon and fatal complication of tracheal or aortic surgery, especially among pediatric patients.

CASE PRESENTATION

We reported a case in a 1-year-old boy with dextrocardia, left pulmonary artery sling and long segment tracheal stenosis. He received slide tracheoplasty at 9 months of age and had post-operative refractory granulation at distal trachea status post repeated balloon dilatation and laser vaporization. Episodes of hemoptysis occurred on post-operative day 81. Bronchoscopy revealed a pulsating pseudoaneurysm at lower trachea which ruptured during the procedure Urgent surgical repair under cardiopulmonary bypass with deep hypothermic circulatory arrest was done. No recurrent bleeding or significant neurologic deficits noticed at a 4-month follow-up.

CONCLUSION

Congenital anomaly that changes the spatial relationship between trachea and aorta could have contributed to formation of ATF. This warrant future attention when managing tracheal granulation with this not uncommon anatomy.

摘要

背景

主动脉-气管瘘(ATF)是气管或主动脉手术后少见但致命的并发症,尤其在儿科患者中更为常见。

病例介绍

我们报告了一例 1 岁男孩的病例,该男孩患有右位心、左肺动脉吊带和长段气管狭窄。他在 9 个月大时接受了滑式气管成形术,术后远端气管出现难治性肉芽组织,在经历了多次球囊扩张和激光汽化后仍未得到缓解。术后第 81 天出现咯血。支气管镜检查发现下气管有搏动性假性动脉瘤,在手术过程中破裂。在体外循环和深低温循环停止下进行紧急手术修复。在 4 个月的随访中,未发现再次出血或明显的神经功能缺损。

结论

改变气管和主动脉空间关系的先天性异常可能导致 ATF 的形成。在处理具有这种常见解剖结构的气管肉芽组织时,这需要引起未来的关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2dd/8011094/dc0840f63d4f/13019_2021_1438_Fig1_HTML.jpg

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