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先天性气管异常:运用连续大体切片的病理学研究及文献综述

Congenital tracheal anomalies: pathology study using serial macrosections and review of the literature.

作者信息

Chen J C, Holinger L D

机构信息

Department of Otolaryngology, National Taiwan University Hospital, Taipei, Republic of China.

出版信息

Pediatr Pathol. 1994 May-Jun;14(3):513-37. doi: 10.3109/15513819409024281.

Abstract

This description of congenital tracheal lesions is presented with a focus on the information derived from the specimens collected for the Laryngeal Development Laboratory at the Children's Memorial Hospital in Chicago from 1975 to 1992. During this period, 115 laryngotracheal specimens were obtained, 22 of which were found to have congenital tracheal anomalies. Six specimens were determined to have tracheomalacia, including one with primary tracheomalacia and five with secondary tracheomalacia: three were associated with tracheoesophageal fistula and two with aberrant innominate artery. Thirteen specimens had a trapped first tracheal arch; one, complete tracheal rings; and two, tracheal cartilaginous sleeve. Three specimens had tracheal agenesis, and three, tracheoesophageal fistula. Some specimens have more than one tracheal anomaly. Sixteen patients also had anomalies of other systems.

摘要

本文对先天性气管病变的描述重点在于1975年至1992年期间从芝加哥儿童纪念医院喉发育实验室收集的标本中获取的信息。在此期间,共获得115份喉气管标本,其中22份被发现存在先天性气管异常。6份标本被确定为气管软化,其中1份为原发性气管软化,5份为继发性气管软化:3份与气管食管瘘相关,2份与迷走无名动脉相关。13份标本存在第一气管弓陷闭;1份为完整气管环;2份为气管软骨套。3份标本为气管缺如,3份为气管食管瘘。部分标本存在不止一种气管异常。16名患者还存在其他系统的异常。

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