Ibrahim N B, Sandry R J
Thorax. 1981 Jun;36(6):465-8. doi: 10.1136/thx.36.6.465.
Congenital oesophageal stenosis caused by heterotopic cartilage and other tracheobronchial structures in the oesophageal wall is a very rare condition. The first case was described by Frey and Duschl in 1936, and only 16 further cases have been reported since that date. We report two further cases of the anomaly. The first, like the majority described previously, was an isolated defect in an otherwise normal child. The second was associated with an oesophageal atresia with a tracheooesophageal fistula and multiple developmental anomalies of the gastrointestinal tract.
由食管壁内异位软骨及其他气管支气管结构引起的先天性食管狭窄是一种非常罕见的病症。首例病例由弗雷和杜施尔于1936年描述,自那时起仅又报道了16例。我们报告另外两例该异常病例。第一例与之前描述的大多数病例一样,是一名其他方面正常儿童的孤立缺陷。第二例与食管闭锁合并气管食管瘘及胃肠道多处发育异常有关。