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首页> 外文期刊>International journal of pediatric otorhinolaryngology >Congenital right bronchial stenosis with high bifurcation: Successful management with side to side tracheobronchial anastomosis
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Congenital right bronchial stenosis with high bifurcation: Successful management with side to side tracheobronchial anastomosis

机译:先天性右支气管狭窄,高分分叉:成功的管理与侧面的气管吻合术

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摘要

Congenital bronchial stenosis is a rare entity [1,2]. While there are some reports of congenital bronchial anomalies and their repair in the thoracic literature this is first report in the literature of a bronchial take off just below the larynx managed with surgical success. Here we present a case of a former 33-weeker born with a tracheoesophageal fistula, Tetralogy of Fallot, and a high bifurcation of the right mainstem bronchus with a concomitant long segment bronchial stenosis. Preoperative planning included printing 3-D reconstructed models of the airway to analyze various treatment options. At 3 months of age the patient was taken to the operating room for surgical repair of the Tetralogy of Fallot and side-to-side tracheobroncheoplasty. The patient was extubated on postoperative day 3 and was discharged home without need for any ventilatory support.
机译:先天性支气管狭窄是一种罕见的实体[1,2]。 虽然有一些先天性支气管异常的报道及其在胸部文献中的修复,这是在喉部下方的支气管脱落的一篇文献中的第一个报告,喉部脱离了手术成功。 在这里,我们提出了一个前33周的案例出生,出生于气管瘘,Tetralogy的椎间盘,以及具有伴随的长段支气管狭窄的右主干支气管的高分分叉。 术前规划包括印刷3-D重建的气道模型来分析各种治疗方案。 在3个月的年龄左右,患者被带到手术室,用于外科手术修复的椎间盘和侧面的气管般成形术。 患者在术后第3天在术后拔下,并在不需要任何通风载体的情况下排出回家。

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