Deiraniya A K
Thorax. 1974 Nov;29(6):720-5. doi: 10.1136/thx.29.6.720.
, , 720-725. Two cases of distal oesophageal obstruction due to tracheobronchial remnant after the successful treatment of proximal oesophageal atresia with an associated tracheo-oesophageal fistula are reported. This association of congenital distal oesophageal stenosis due to tracheobronchial remnant with oesophageal atresia and tracheo-oesophageal fistula has not previously been reported in the literature. The diagnosis should be suspected in cases of distal oesophageal obstruction presenting in childhood or adult life with a history dating back to infancy or childhood. Radiologically a short stenotic non-relaxing segment is the hallmark. There is no hiatus hernia and no gastro-oesophageal reflux. Surgical excision is recommended and can be achieved easily through a thoracic approach. Dilatation is difficult, at times impossible and occasionally hazardous, and any benefit is transient. Excision of the stenotic segment with primary end-to-end anastomosis is the method of choice and almost always possible.
报道了2例近端食管闭锁合并气管食管瘘成功治疗后因气管支气管残余导致远端食管梗阻的病例。先天性远端食管狭窄由气管支气管残余引起,与食管闭锁和气管食管瘘相关联,此前文献中未见报道。对于儿童期或成年期出现远端食管梗阻且病史可追溯至婴儿期或儿童期的病例,应怀疑此病。放射学上,短的狭窄且不松弛的节段是其特征。无食管裂孔疝且无胃食管反流。建议手术切除,可通过开胸手术轻松实现。扩张困难,有时无法进行,偶尔有危险,且任何益处都是短暂的。切除狭窄节段并进行端端吻合是首选方法,且几乎总是可行的。 720 - 725页。