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腹腔镜辅助下肝外胆管切除、胆管成形术及扩大的肝管空肠吻合术治疗复杂性肝胆管扩张症。

Laparoscopically assisted extrahepatic bile duct excision with ductoplasty and a widened hepaticojejunostomy for complicated hepatobiliary dilatation.

作者信息

Li Suolin, Wang Wenbo, Yu Zengwen, Xu Weili

机构信息

Department of Pediatric Surgery, The Second Hospital of Hebei Medical University, 215# Hepingxi Road, Shijiazhuang, China,

出版信息

Pediatr Surg Int. 2014 Jun;30(6):593-8. doi: 10.1007/s00383-014-3501-2. Epub 2014 Apr 10.

Abstract

BACKGROUND

Complicated hepatobiliary dilatation is characterized by congenital cystic dilatation of the biliary tree extending to involve the intrahepatic biliary channels. Some studies have reported on laparoscopic excision for common choledochal cyst, yet there are little reports on laparoscopic surgery for congenital choledochal cyst with intrahepatic bile duct dilatation. In this paper, we present our experiences in laparoscopic extrahepatic bile duct excision combined with ductoplasty and hepaticojejunostomy for complicated hepatobiliary dilatation.

METHODS

We retrospectively studied 153 children (age ranged between 3 months and 12 years) who had undergone laparoscopic cholangiopancreatography and radical choledochal resection in our institute from 2002 to 2012. A co-existing extra- and intra-hepatic dilatation was found in 26 patients. After resecting the extrahepatic dilated duct and widening the portohepatic or intrahepatic ductal lumen (ductoplasty) under the laparoscopic video, a widened hepaticojejunostomy at the hilum was performed using a Roux-en-Y jejunal limb.

RESULTS

Laparoscopic procedures were successfully performed in all children with complicated hepatobiliary dilatation and their ductal stenoses at the hilum were corrected. In 13 patients with a stricture that converged into the common hepatic duct, the stenotic segment was incised and a wide hepaticojejunostomy was completed at the porta hepatis. A constrictive confluence of the right and left hepatic duct was observed in eight cases, a bi-ductal portojejunostomy was achieved at the bifurcation after making incision in the bilateral stenotic hepatic ducts to create a large stoma. A downstream stricture of the left hepatic duct was identified and incised from the hilum to the dilated segment along the lateral wall in three cases, so that a long hepaticojejunostomy to left intrahepatic duct lay in an oblique orientation. In two cases, a septum was found in the right hepatic ductal terminal and excised through the hilar orifice. Postoperative complications were observed in two children including temporary bile leakage and hepaticojejunal anastomotic stricture each one. The intrahepatic duct dilatation was remarkably reduced in size during the follow-up.

CONCLUSIONS

Laparoscopic cholangiopancreatography is a valuable method in offering an accurate delineation of complicated hepatobiliary dilatation associated pancreaticobiliary maljunction and only necessitates simple equipments. With the aid of the magnified laparoscopic view, the radical resection of extrahepatic biliary duct and correction of the portohepatic bile ductal stenosis can be exactly performed. Laparoscopic hepaticojejunostomy at the hilum is effective and safe for children with complicated hepatobiliary dilatation.

摘要

背景

复杂性肝胆管扩张症的特征是胆管先天性囊性扩张并累及肝内胆管。一些研究报道了腹腔镜下胆总管囊肿切除术,但关于先天性胆总管囊肿合并肝内胆管扩张的腹腔镜手术报道较少。在本文中,我们介绍了腹腔镜下肝外胆管切除联合胆管成形术及肝管空肠吻合术治疗复杂性肝胆管扩张症的经验。

方法

我们回顾性研究了2002年至2012年在我院接受腹腔镜胰胆管造影和根治性胆总管切除术的153例儿童(年龄3个月至12岁)。其中26例存在肝内外胆管同时扩张。在腹腔镜视野下切除肝外扩张胆管并扩大肝门或肝内胆管腔(胆管成形术)后,用Roux-en-Y空肠袢在肝门处进行扩大的肝管空肠吻合术。

结果

所有复杂性肝胆管扩张症患儿均成功实施了腹腔镜手术,其肝门处胆管狭窄得到纠正。13例汇合至肝总管的狭窄患者,切开狭窄段并在肝门处完成广泛的肝管空肠吻合术。8例观察到左右肝管狭窄性汇合,在双侧狭窄肝管切开后在分叉处进行双管肝门空肠吻合术以形成大的吻合口。3例在肝门处发现左肝管下游狭窄并沿侧壁从肝门至扩张段切开,从而使左肝内胆管的长段肝管空肠吻合呈斜位。2例在右肝管末端发现隔膜并通过肝门孔切除。2例患儿出现术后并发症,分别为暂时性胆漏和肝管空肠吻合口狭窄。随访期间肝内胆管扩张明显缩小。

结论

腹腔镜胰胆管造影是准确描绘合并胰胆管连接异常的复杂性肝胆管扩张症的有价值方法,且仅需简单设备。借助放大的腹腔镜视野,可准确实施肝外胆管根治性切除及肝门胆管狭窄矫正。肝门处腹腔镜肝管空肠吻合术对复杂性肝胆管扩张症患儿有效且安全。

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