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[先天性声门-声门下狭窄]

[Congenital glottic-subglottic stenoses].

作者信息

Narcy P, Juvanon J M, Contencin P, Bobin S

出版信息

Ann Otolaryngol Chir Cervicofac. 1985;102(6):443-8.

PMID:4091393
Abstract

One particular form of congenital stenosis of larynx that should be considered as a separate entity is the combination of a glottic stenosis with subglottic retraction. The salient features of this malformation are analyzed in 15 cases: laryngeal dyspnea with dysphonia in 2 of 3 patients and the possible detection of a subglottic anomaly on lateral radiography of larynx. However, confirmation of diagnosis can only be by laryngotracheoscopy. It is important to establish a diagnosis of subglottic stenosis associated with a palmation, since treatment and prognosis are very different from those of an isolated glottic palmation: all attempts at endoscopic treatment resulted in failure that intubation or tracheotomy was necessary in 7 cases. One of the 3 fatal cases was directly related to lack of detection of the subglottic stenosis. A successful laryngoplasty was performed in 10 children.

摘要

一种应被视为独立病症的先天性喉狭窄特殊形式是声门狭窄合并声门下缩窄。对15例这种畸形的显著特征进行了分析:3例患者中有2例出现喉喘鸣伴发音困难,并且在喉部侧位X线片上可能检测到声门下异常。然而,诊断的确认只能通过喉镜气管镜检查。确定与蹼状畸形相关的声门下狭窄的诊断很重要,因为其治疗和预后与孤立的声门蹼状畸形非常不同:所有内镜治疗尝试均失败,7例患者需要插管或气管切开术。3例死亡病例中有1例直接与未检测到声门下狭窄有关。10名儿童成功进行了喉成形术。

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