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后鼻孔闭锁和后鼻孔狭窄。

Choanal atresia and choanal stenosis.

作者信息

Ramsden James D, Campisi Paolo, Forte Vito

机构信息

ENT Department, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK.

出版信息

Otolaryngol Clin North Am. 2009 Apr;42(2):339-52, x. doi: 10.1016/j.otc.2009.01.001.

Abstract

Congenital narrowing of the nasal airway at the posterior choanae, which can be uni- or bilateral, is an uncommon condition in pediatric patients. The surgical management of choanal atresia varies widely in different centers. This article discusses the different surgical strategies including: dilation and stenting; trans-palatal repair; and transnasal resection utilizing endoscopic sinus surgery (ESS) techniques. The merits of stents, lasers, CT-guided surgery, and the use of additional agents including mitomycin C are reviewed, as well as the particular problems associated with managing bilateral choanal atresia in neonates.

摘要

后鼻孔处先天性鼻气道狭窄,可为单侧或双侧,在儿科患者中是一种罕见病症。不同中心对后鼻孔闭锁的手术治疗差异很大。本文讨论了不同的手术策略,包括:扩张和支架置入;经腭修复;以及利用鼻内镜鼻窦手术(ESS)技术进行经鼻切除。文中还综述了支架、激光、CT引导手术以及包括丝裂霉素C在内的其他药物的优点,以及新生儿双侧后鼻孔闭锁治疗中存在的特殊问题。

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