Manson D, Filler R, Gordon R
Department of Diagnostic Imaging, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8.
Pediatr Radiol. 1996;26(6):427-30. doi: 10.1007/BF01387321.
Two cases of congenital tracheal stenosis were managed conservatively despite mild to moderate initial respiratory symptomatology in infancy. Serial CT examinations were performed on each child, with tracheal dimensions and cross-sectional areas measured in the region of stenosis at each CT examination. The examinations document increases in tracheal cross-sectional area in the region of stenosis over time, confirming tracheal cartilage growth. We present these data to dispel the hypothesis that tracheal growth does not occur in complete-ring tracheal stenosis. The selection of cases for surgical repair must be considered with the knowledge that this anomaly does not carry an inevitably poor prognosis.
两例先天性气管狭窄患儿在婴儿期虽有轻度至中度初始呼吸道症状,但采用了保守治疗。对每个患儿进行了系列CT检查,每次CT检查时均在狭窄区域测量气管尺寸和横截面积。检查记录显示,狭窄区域的气管横截面积随时间增加,证实了气管软骨的生长。我们展示这些数据以消除关于完全环状气管狭窄中气管不会生长的假说。在选择手术修复病例时,必须认识到这种异常情况并非必然预后不良。