Jona J Z, Belin R P
J Pediatr Surg. 1977 Apr;12(2):227-32. doi: 10.1016/s0022-3468(77)80012-2.
This is a report of the fourth known case of intramural TEF with diaphragmatic esophageal atresia. These patients present clinically as a typical esophageal atresia with tracheoesophageal fistula, but in effect have the following unusual features: 1) high TEF entering the trachea in the neck; 2) diaphragmatic-type atresia of the esophagus with uninterrupted muscular coat; 3) the location of this diaphragm is at the level of the carina producing in effect a long intramural fistulous tract. It is believed that faulty recannulization of a segment of the esophagus in association with H-type TEF may explain this uncommon anomaly.
这是第四例已知的伴有膈膜型食管闭锁的壁内气管食管瘘病例报告。这些患者临床上表现为典型的食管闭锁合并气管食管瘘,但实际上具有以下不寻常特征:1)高位气管食管瘘,瘘口位于颈部气管;2)食管呈膈膜型闭锁,肌层连续;3)该膈膜位于气管隆突水平,实际上形成了一条长的壁内瘘管。据信,食管某段再通异常合并H型气管食管瘘可能解释了这种罕见的异常情况。