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先天性咽喉带:一例罕见的呼吸窘迫病例报告。

Congenital pharyngolaryngeal band: report of an unusual case of respiratory distress.

作者信息

Fayoux P, Vachin F, Merrot O, Chevalier D, Robert Y

机构信息

Service d'ORL et Chirurgie Cervicofaciale, Hôpital Claude Huriez--CHRU Lille, 2 Ave Oscar Lambret, Lille 59037, France.

出版信息

Int J Pediatr Otorhinolaryngol. 2003 Dec;67(12):1379-81. doi: 10.1016/j.ijporl.2003.07.003.

Abstract

Congenital pharyngolaryngeal band (PLB) is an extremely rare congenital abnormality, characterized by a fibrous web extending from the nasopharynx to the epiglottis. We report a case of unilateral pharyngolaryngeal band in a new-born who presented severe airway obstruction and feeding difficulties. The band extended from the right postero-inferior part of the nasopharynx to the right lateral margin of the larynx. Faucial pillars and tonsil were absent on this side. Endoscopic and radiological assessments excluded associated cervicofacial abnormality. Two endoscopic laser resection procedures were necessary to liberate the larynx from PLB. Clinical and radiological assessment advocated a second pharyngeal pouch development failure as the origin to PLB.

摘要

先天性咽喉带(PLB)是一种极其罕见的先天性异常,其特征是有一个从鼻咽延伸至会厌的纤维网。我们报告一例新生儿单侧咽喉带病例,该患儿出现严重气道阻塞和喂养困难。该带从鼻咽右后下部延伸至喉的右侧边缘。此侧腭弓和扁桃体缺如。内镜和影像学评估排除了相关的颈面部异常。需要进行两次内镜激光切除手术以将喉部从咽喉带中解放出来。临床和影像学评估认为第二咽囊发育失败是咽喉带的起源。

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