Iuchtman M, Sternberg A, Iurman S
Dept. of Surgery A, Hillel Jaffe Medical Center, Hadera.
Harefuah. 1991 Mar 1;120(5):263-4.
A 2.5 kg female neonate, born after a normal 39-week pregnancy to Arab parents (1st degree cousins), developed unremitting vomiting of gastric contents, not bile-stained. Barium study demonstrated a grossly distended stomach with complete obstruction of the outlet. At laparotomy, pyloric atresia and a heterotopic pancreas located subserosally on the antrum of the stomach were diagnosed. A 3-cm gap was measured between the occluded antrum and the duodenum. Transmesocolic gastrojejunostomy was performed, and oral feeding was started 5 days later. Pyloric atresia and heterotopic pancreas are both rare congenital malformations. To the best of our knowledge, the combination of pyloric atresia and heterotopic pancreas has not previously been reported.
一名2.5千克的女新生儿,在39周正常孕期后出生,父母为阿拉伯人(一级表亲),出现持续呕吐胃内容物,无胆汁染色。钡餐检查显示胃明显扩张,出口完全梗阻。剖腹手术时,诊断为幽门闭锁和位于胃窦浆膜下的异位胰腺。在闭锁的胃窦和十二指肠之间测量出3厘米的间隙。进行了经结肠系膜胃空肠吻合术,5天后开始经口喂养。幽门闭锁和异位胰腺都是罕见的先天性畸形。据我们所知,此前尚未有幽门闭锁和异位胰腺合并出现的报道。