Hemalatha V, Batcup G, Brereton R J, Spitz L
J Pediatr Surg. 1980 Apr;15(2):178-80. doi: 10.1016/s0022-3468(80)80012-1.
Intrathoracic foregut duplication cysts are rare congenital foregut malformations that usually produce respiratory symptoms in early infancy. Surgical resection of this anomaly is usually followed by permanent cure. Two cases of intrathoracic foregut duplication cyst associated with esophageal atresia are reported. The first patient had an associated tracheoesophageal fistula while the second had an isolated atresia. Both patients survived following resection of the cysts.
胸内前肠重复囊肿是罕见的先天性前肠畸形，通常在婴儿早期出现呼吸道症状。手术切除这种异常通常可实现永久性治愈。本文报告了两例与食管闭锁相关的胸内前肠重复囊肿病例。第一例患者伴有气管食管瘘，第二例患者为单纯性闭锁。两例患者在囊肿切除后均存活。
