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Preoperative Tracheoscopy for Esophageal Atresia and/or Congenital Esoaerian Fistula: Experience at Cliniques Universitaires Saint Luc in Brussels

机译:食管闭锁和/或先天性食管瘘的术前气管镜检查:布鲁塞尔圣卢克诊所的经验

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Introduction: Congenital septal anomalies between the trachea and the esophagus are rare conditions. It seemed to us interesting to recall the contribution of tracheoscopy in the diagnostic and therapeutic strategy of esophageal atresia and congenital esoaerian fistulas. Patients and methods: This is a retrospective study between June 1994 and June 2014 of children who underwent a tracheoscopy, at the Saint-Luc University Clinics in Brussels, the diagnostic set of esophageal atresia (EA) or a congenital esoaerian fistula was suspected. Results: A total of 43 children with esophageal atresia or congenital esoaerian fistula underwent tracheoscopy. Before the tracheoscopy, the diagnosis of the anatomical type of atresia of the esophagus and esoaerian fistula was as follows: type C, 34 (79.1%); type A, 4 (9.3%); type E, 5 (11.6%). After performing the tracheoscopy, the diagnosis was changed as follows: type C, 34 (79.1%); type A, 3 (7%); type E, 4 (9.3%); type B, 1 (2.3%), a patient with a tracheoesophageal laryngo cleft (2.3%). Tracheoscopy also made it possible to find 2 cases of tracheomalacia, 2 cases with 3 bronchial tubes and one case associating a diverticulum of the trachea. No complications were correlated with the performance of the tracheoscopy. Conclusion: Our study confirms the benefits of tracheoscopy in the laden price of esophageal atresia or congenital esoaerian fistula.
机译:简介:气管和食道之间的先天性间隔异常是罕见的情况。在我们看来,回顾气管镜在食管闭锁和先天性食管瘘的诊断和治疗策略中的贡献似乎很有趣。患者和方法:这是一项对1994年6月至2014年6月在布鲁塞尔的圣卢克大学诊所接受气管镜检查的儿童进行的回顾性研究,怀疑是诊断性食管闭锁(EA)或先天性食管瘘。结果:总共有43例患有食管闭锁或先天性食管瘘的儿童接受了气管镜检查。气管镜检查前,对食管和食管瘘的闭锁的解剖类型的诊断如下:C型34例(79.1%); A型,4(9.3%); E型5(11.6%)。进行气管镜检查后,诊断改变如下:C型,34(79.1%); A型,3(7%); E型,4(9.3%); B型1例(2.3%),气管食管喉裂(2.3%)。气管镜检查还可以发现2例气管软化症,2例带有3支支气管的导管和1例伴有气管憩室的病例。气管镜检查无并发症发生。结论:我们的研究证实了气管镜检查在食管闭锁或先天性食管瘘的高昂价格中的优势。

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