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儿童先天性软骨套管状气管的管理

Management of congenital cartilaginous sleeve trachea in children.

作者信息

Hamilton Jane, Clement W Andrew, Kubba Haytham

机构信息

University of Glasgow, Scotland, United Kingdom.

Department of Otolaryngology - Head and Neck Surgery, Royal Hospital for Sick Children, Glasgow G3 8SJ, Scotland, United Kingdom.

出版信息

Int J Pediatr Otorhinolaryngol. 2014 Nov;78(11):2011-4. doi: 10.1016/j.ijporl.2014.08.031. Epub 2014 Sep 1.

Abstract

AIMS

Children with congenital tracheal cartilaginous sleeve may present to otolaryngology services with airway problems. We wish to describe our overall management in a series of four children with this very rare anomaly.

METHODS

Retrospective case note review of children diagnosed with congenital tracheal cartilaginous sleeve presenting to our department between 2006 and 2014.

RESULTS

Four patients were seen. One had Opitz G syndrome, two had Pfeiffers syndrome and one had no associated anomalies. Two children were successfully managed with laryngeal reconstruction using an anterior costal cartilage graft, while the third and fourth required a short period of tracheostomy only. All four are well and currently asymptomatic from an airway point of view.

CONCLUSION

Congenital tracheal cartilaginous sleeve is a very rare and potentially challenging problem. Otolaryngologists should be aware that it can occur in children with syndromes other than craniosynostosis (and indeed, those with no syndrome) and that it can be successfully treated using established airway management techniques.

ETHICAL APPROVAL

Registered with Clinical Governance Committee.

摘要

目的

患有先天性气管软骨套的儿童可能因气道问题就诊于耳鼻喉科。我们希望描述我们对一系列四名患有这种极为罕见异常的儿童的总体治疗情况。

方法

对2006年至2014年间在我们科室诊断为先天性气管软骨套的儿童进行回顾性病例记录审查。

结果

共诊治了四名患者。一名患有奥匹兹G综合征,两名患有 Pfeiffer 综合征,一名无相关异常。两名儿童通过使用前肋软骨移植进行喉重建成功治疗,而第三名和第四名仅需要短期气管切开术。从气道角度来看,所有四名患者目前情况良好且无症状。

结论

先天性气管软骨套是一个非常罕见且具有潜在挑战性的问题。耳鼻喉科医生应意识到它可发生于除颅缝早闭综合征之外的儿童(实际上,也可发生于无综合征的儿童),并且可以使用既定的气道管理技术成功治疗。

伦理批准

已在临床治理委员会注册。

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