先天性喉气管食管裂

J Pediatr Surg. 1976 Dec;11(6):933-7. doi: 10.1016/s0022-3468(76)80069-3.

Two infants with complete laryngotracheoesophageal cleft are presented. One infant had hypoplasia of the left bronchus and lung and the other had a cystic dysplastic right kidney. The literature is reviewed and a scheme for managing infants with this severe and as yet lethal anomaly is presented.

本文报告了两名患有完全性喉气管食管裂的婴儿。一名婴儿存在左支气管和肺发育不全，另一名婴儿患有右侧肾囊性发育不良。对相关文献进行了综述，并提出了一种针对这种严重且迄今仍致命的畸形婴儿的治疗方案。