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Congenital esophageal stenosis because of tracheobronchial remnant and treated by circular myectomy: a case report.

机译:因气管支气管残余而导致的先天性食管狭窄,并通过圆环肌切除术治疗:1例。

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摘要

Congenital esophageal stenosis (CES) is a rare anomaly, and appropriate management is not well established. We performed myectomy of the esophageal wall in a child with critical esophageal stenosis caused by tracheobronchial remnant (TBR). An 18-month-old boy was admitted to our hospital having frequent vomiting and failure to thrive. Esophagography and esophagoscopy showed abrupt stenosis at the lower esophageal wall. Balloon dilatation was performed but was ineffective. Surgery was performed under a diagnosis of CES because of TBR. Cartilage was palpable in the stenotic esophageal wall, and extirpation of the muscular layer of the stenotic portion was performed, leaving the mucosal layer intact. The muscular layer was closed loosely using interrupted 5-0 absorbable sutures to match the oral and anal sides together. Postoperatively, the esophageal passage was improved to the point that the patient was able to take solid foods without vomiting. This successful outcome suggests that circular myectomy ofthe TBR is worth recommending as a surgical procedure for short segment and stenosis of patients with CES because of TBR.
机译:先天性食管狭窄(CES)是一种罕见的异常,尚无适当的治疗方法。我们对由气管支气管残余(TBR)引起的严重食管狭窄的儿童进行了食管壁肌切除术。一名18个月大的男孩因呕吐频繁且未能failure壮成长,被送入我们的医院。食管造影和食管镜检查显示食管下壁突然狭窄。进行了球囊扩张术,但无效。由于TBR,在CES的诊断下进行了手术。在狭窄的食管壁可触及软骨,并切除狭窄部分的肌肉层,使粘膜层完整。使用间断的5-0可吸收缝线将肌肉层松散地闭合,以使口腔和肛门两侧配合在一起。术后食管通道得到了改善,以至于患者可以不呕吐地摄取固体食物。这一成功的结果表明,值得推荐的是TBR环形肌切除术作为因TBR而导致CES患者的短节段和狭窄的手术方法。

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