Suppr超能文献

先天性气管环完全缺如伴三叉形隆突:罕见临床及内镜表现的病例报告

Congenital complete absence of tracheal rings with trifurcate carina: Case report of a rare clinical and endoscopic presentation.

作者信息

Schwartz Isaac E, Utz Edward R, Gaudreau Philip A

机构信息

Department of Otolaryngology/Head & Neck Surgery, Naval Medical Center San Diego, San Diego, CA, United States.

Department of Otolaryngology/Head & Neck Surgery, Naval Medical Center San Diego, San Diego, CA, United States.

出版信息

Int J Pediatr Otorhinolaryngol. 2018 Aug;111:1-6. doi: 10.1016/j.ijporl.2018.05.009. Epub 2018 May 24.

Abstract

We describe the case of a child with isolated absence of cartilaginous tracheal rings and a trifurcate carina. At 6 months of age, the patient presented to our multidisciplinary airway clinic with stridor and recurrent severe respiratory infections requiring hospitalization. Radiographs showed airway narrowing. Exam demonstrated biphasic stridor. Flexible fiberoptic laryngoscopy demonstrated only mild laryngomalacia. Operative bronchoscopy demonstrated severe tracheomalacia with absence of any visible tracheal rings and a trifurcate carina. Subsequent CT imaging corroborated these findings and did not demonstrate any other major abnormality. The patient did not require operative intervention and his subsequent course was uncomplicated.

摘要

我们描述了一名患有孤立性软骨气管环缺如和三叉形隆突的儿童病例。6个月大时,该患者因喘鸣和反复严重呼吸道感染需住院治疗,前来我们的多学科气道诊所就诊。X线片显示气道狭窄。检查发现双相喘鸣。可弯曲纤维喉镜检查仅显示轻度喉软化。手术支气管镜检查显示严重气管软化,未见任何可见的气管环,且有三叉形隆突。随后的CT成像证实了这些发现,未显示任何其他主要异常。该患者无需手术干预,其后续病程无并发症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验