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双侧先天性后鼻孔闭锁的经验

Experience with bilateral congenital atresia of the posterior nasal choanae.

作者信息

Prescott C A

出版信息

J Laryngol Otol. 1986 Nov;100(11):1255-61. doi: 10.1017/s0022215100100933.

Abstract

Atresia of the posterior nasal choanae is an unusual congenital condition. The embryological explanation is uncertain, that felt to be the most probable being presented here. Bilateral choanal atresia tends to be associated with neonatal airways obstruction and steps to be taken in its diagnosis and management are outlined. The definitive treatment of the condition is surgical excision, by either a trans-nasal or a trans-palatal approach. The conclusions arrived at as to the most effective method of management of these cases from a personal series of fourteen cases are detailed. A preference for the trans-nasal surgical approach is indicated and surgical details for this method are given, some aspects of which have not been previously reported.

摘要

后鼻孔闭锁是一种罕见的先天性疾病。胚胎学解释尚不确定,此处给出最可能的解释。双侧后鼻孔闭锁往往与新生儿气道阻塞有关,并概述了其诊断和处理措施。该疾病的确定性治疗方法是手术切除,可采用经鼻或经腭入路。详细介绍了从个人的14例病例系列中得出的关于这些病例最有效治疗方法的结论。表明了对经鼻手术入路的偏好,并给出了该方法的手术细节,其中一些方面此前尚未有报道。

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