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Initial experience with complex laparoscopic biliary surgery in children: biliary atresia and choledochal cyst.

机译:儿童复杂腹腔镜胆道手术的初步经验:胆道闭锁和胆总管囊肿。

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BACKGROUND: Laparoscopic approaches are possible for many pediatric surgical diseases, including complex biliary disorders. The authors describe their early experience with laparoscopic procedures for biliary atresia and choledochal cysts. METHODS: A retrospective review was performed with Institutional Review Board (IRB) approval of children undergoing laparoscopic Kasai portoenterostomy (n = 2) or laparoscopic excision of a choledochal cyst with Roux-en-y biliary reconstruction (n = 3). The authors report the operative technique for these procedures and present their initial results. RESULTS: All procedures were performed with 4 to 5 trocars using 3- and 5-mm ports. Excision of the fibrous biliary remnant (biliary atresia) or of the cyst (choledochal cysts) was performed laparoscopically in all cases. The Roux-en-y limb was created through a 1-cm extension of the umbilical port site. Laparoscopic biliary reconstruction was performed successfully in 4 of 5 patients. In one child, the proximal extent of the choledochal cyst was at the bifurcation of the hepatic duct, and the biliary reconstruction was performed via an open incision with separate anastomoses of the right and left ducts. The gallbladder was used as a handle for retraction of the liver for portal visualization, as in a cholecystectomy, and was resected at the end of the procedure. All children with choledochal cysts have normal bilirubin values. One of 2 children who underwent laparoscopic Kasai has a normal postoperative bilirubin level, whereas the other child did not drain bile and underwent a successful liver transplantation. Mean length of surgery was 338 minutes; mean length of stay was 5.5 days. There were no significant postoperative complications. Cosmesis was excellent in all cases. CONCLUSIONS: Laparoscopic approaches for children with biliary atresia and choledochal cysts are possible. Excellent visualization of the portal structures can be achieved laparoscopically with adequate retraction of the liver. Further follow-up is needed to determine broader application.
机译:背景:腹腔镜手术方法可用于许多儿科手术疾病,包括复杂的胆道疾病。作者介绍了他们的腹腔镜手术治疗胆道闭锁和胆总管囊肿的早期经验。方法:对接受腹腔镜Kasai腔肠造口术(n = 2)或腹腔镜切除胆总管囊肿并经Roux-en-y胆道重建术(n = 3)的儿童进行回顾性审查,并获得了机构审查委员会(IRB)的批准。作者报告了这些程序的手术技术,并介绍了他们的初步结果。结果:所有手术均使用3毫米和5毫米端口使用4至5根套管针进行。在所有情况下,均通过腹腔镜切除纤维性胆道残余物(胆道闭锁)或囊肿(胆道囊肿)。 Roux-en-y肢体是通过脐部端口部位的1厘米延伸形成的。 5例患者中有4例成功进行了腹腔镜胆道重建术。在一个儿童中,胆总管囊肿的近端范围位于肝管的分叉处,并通过一个开放的切口进行胆道重建,左右导管分别吻合。如在胆囊切除术中一样,胆囊被用作肝门回缩的手柄,并在胆囊切除术中被切除。所有胆总管囊肿患儿的胆红素值均正常。接受腹腔镜开赛手术的2名患儿中,一名患儿的胆红素水平正常,而另一名患儿未排空胆汁并成功进行了肝移植。平均手术时间为338分钟;平均住院时间为5.5天。术后无明显并发症。在所有情况下美容效果都很好。结论:腹腔镜治疗胆道闭锁和胆总管囊肿的儿童是可行的。腹腔镜可以使肝脏充分回缩,从而实现门静脉结构的出色可视化。需要进一步跟踪以确定更广泛的应用。

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