Heij H A, Niessen G J
Department of Pediatric Surgery, Sophia Children's Hospital, Rotterdam, Netherlands.
J Pediatr Surg. 1987 Nov;22(11):1033. doi: 10.1016/s0022-3468(87)80511-0.
The association of annular pancreas with biliary tract anomalies is extremely rare. A patient is reported with annular pancreas, congenital absence of the gallbladder, and dilation of the common bile duct. Surgical correction of the duodenal obstruction was performed and intraoperative cholangiography was done. Recovery was uneventful and long-term liver function remained normal.
环状胰腺合并胆道异常极为罕见。本文报道了一例患有环状胰腺、先天性胆囊缺如及胆总管扩张的患者。对十二指肠梗阻进行了手术矫正,并进行了术中胆管造影。患者恢复顺利,长期肝功能保持正常。