Anderson K D, Guzzetta P C
J Pediatr Surg. 1983 Dec;18(6):747-50. doi: 10.1016/s0022-3468(83)80017-7.
Two children with congenital microgastria and associated anomalies requiring surgery as infants, developed severe dumping syndrome which necessitated a remedial operation. A Roux-en-Y jejunal pouch (Hunt-Lawrence) was formed at 22 months and 10 months respectively. Weight gain was immediate in both patients and has been sustained for 6 months and 8 years respectively. Symptoms of the dumping syndrome were relieved and the pouch delays filling of the jejunum.
两名患有先天性小胃并伴有相关异常的儿童在婴儿期需要进行手术，术后出现了严重的倾倒综合征，这使得必须进行补救手术。分别在22个月和10个月时形成了Roux-en-Y空肠袋（亨特-劳伦斯式）。两名患者体重均立即增加，分别持续了6个月和8年。倾倒综合征的症状得到缓解，且该肠袋延缓了空肠的充盈。
