Morgan C L, Grossman H, Leonidas J
Clin Radiol. 1979 May;30(3):353-8. doi: 10.1016/s0009-9260(79)80101-4.
Roentgenographic and clinical findings in a spectrum of malformations of the trachea and oesophagus are discussed. Five previously unreported patients representing four rare anomalies of tracheal agenesis, laryngotracheo-oesophageal cleft, oesophageal atresia with a tracheo-oesophageal (T-E) fistula to the proximal oesophageal pouch, and T-E fistula without oesophageal atresia (H-type fistula) are presented. These anomalies can be characterised by a failure in separation of the oesophagus and trachea and by atresia of either organ. All of the patients were diagnosed roentgenographically. Since the incidence of associated abnormalities is high in babies with these anomalies, a generalised embryological defect must be a basic assumption in any theory to explain the development of T-E anomalies.
本文讨论了一系列气管和食管畸形的X线及临床检查结果。介绍了五例先前未报道的患者,分别代表四种罕见的异常情况:气管闭锁、喉气管食管裂、食管闭锁伴气管食管(T-E)瘘至食管近端盲袋,以及无食管闭锁的T-E瘘(H型瘘)。这些异常的特征可能是食管和气管分离失败以及任一器官闭锁。所有患者均通过X线检查确诊。由于患有这些异常的婴儿中相关异常的发生率较高,在任何解释T-E异常发育的理论中,普遍的胚胎学缺陷必定是一个基本假设。