Suppr超能文献

先天性气管蹼——一例报告

Congenital tracheal web--a case report.

作者信息

Miller B J, Morrison M D

出版信息

J Otolaryngol. 1978 Jun;7(3):218-22.

PMID:691088
Abstract

Congenital tracheal webs are rare. This report involves an eight year old girl presenting with a six year history of frequent colds, wheezing, and dyspnea in whom the tracheal web was successfully excised after failure of bronchoscopic dilation. Tracheal embryology is briefly reviewed and tracheal stenoses are classified. A history of recurrent chest infection and finding of stridor are the chief of recurrent chest infection and the finding of stridor are the chief features ot his lesion. Lateral chest roentgenogram, tracheal tomography, and bronchoscopy are useful in establishing the diagnosis.

摘要

先天性气管蹼很少见。本报告涉及一名8岁女孩,有6年频繁感冒、喘息和呼吸困难病史,在支气管镜扩张失败后成功切除气管蹼。简要回顾了气管胚胎学并对气管狭窄进行了分类。反复胸部感染病史和喘鸣音是其病变的主要特征。胸部侧位X线片、气管体层摄影术和支气管镜检查有助于确诊。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验