小儿肝移植手术中腔门半肝切除术治疗完全性门-肠静脉血栓形成的十年随访:病例报告和文献综述。

IF 1.2 4区 医学 Q3 PEDIATRICS
John O Barron, Kadakkal Radhakrishnan, Christopher Coppa, Deborah Goldman, Vera Hupertz, Mike Leonis, Bijan Eghtesad, Koji Hashimoto
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引用次数: 0

摘要

背景:门静脉血栓是小儿肝移植术后可能出现的严重并发症。在极少数门-肠管完全血栓形成的情况下,腔门半肝切除术可提供移植物血流。在此,我们描述了一例小儿肝移植过程中腔门半肝切开术的长期结果,并回顾了目前的儿科文献:一名 9 个月大的女性患者因胆道闭锁和卡萨伊肠门造口术失败而接受了活体肝移植手术,手术因肠门静脉血栓形成而变得复杂。患者在术后第 12 天接受了再次移植,并进行了腔门肝移植:患者康复后未再出现并发症,10 年后,她的情况依然良好,移植物功能正常,未出现门静脉高压的临床后遗症。三维血管重建 CT 扫描显示脾脏系统重新闭塞,通过肠系膜下静脉分流系统引流至下腔静脉。腔门吻合口保持通畅,并有肝瓣血流。在之前报道的12例小儿肝移植中作为门静脉流入的腔门肝吻合术病例中,这是已知的随访时间最长的一例存活的同种异体肝移植。值得注意的是,门静脉高压后遗症在之前报道的12例病例中也很少见,没有出现长期肾功能障碍、下肢水肿或腹水的病例:结论:小儿腔门肝移植术后,移植器官功能正常且长期存活超过 10 年是可行的。与门静脉高压相关的并发症一般持续时间较短,这可能是由于侧支循环的稳健发展。有必要提供更多有关长期结果的报告,以便在考虑将小儿腔门有瓣肝移植术用于肝脏流入时做出明智的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ten-year follow-up of cavoportal hemitransposition in pediatric liver transplantation for complete portomesenteric venous thrombosis: A case report and literature review.

Background: Portal vein thrombosis is a potentially devastating complication following pediatric liver transplantation. In rare instances of complete portomesenteric thrombosis, cavoportal hemitransposition may provide graft inflow. Here we describe long-term results following a case of pediatric cavoportal hemitransposition during liver transplantation and review the current pediatric literature.

Methods: A 9-month-old female with a history of biliary atresia and failed Kasai portoenterostomy underwent living donor liver transplantation, which was complicated by portomesenteric venous thrombosis. The patient underwent retransplantation with cavoportal hemitransposition on postoperative day 12.

Outcome: The patient recovered without further complication, and 10 years later, she continues to do well, with normal graft function and no clinical sequelae of portal hypertension. CT scan with 3-D vascular reconstruction demonstrated recanalization of the splanchnic system, with systemic drainage to the inferior vena cava via an inferior mesenteric vein shunt. The cavoportal anastomosis remains patent with hepatopetal flow. Of the 12 previously reported cases of pediatric cavoportal hemitransposition as portal inflow in liver transplantation, this is the longest-known follow-up with a viable allograft. Notably, sequelae of portal hypertension were also rare in the 12 previously reported cases, with no cases of long-term renal dysfunction, lower extremity edema, or ascites.

Conclusions: Long-term survival beyond 10 years with normal graft function is feasible following pediatric cavoportal hemitransposition. Complications related to portal hypertension were generally short-lived, likely due to the development of robust collateral circulation. Additional reports of long-term outcomes are necessary to facilitate informed decision making when considering pediatric cavoportal hemitransposition for liver graft inflow.

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来源期刊
Pediatric Transplantation
Pediatric Transplantation 医学-小儿科
CiteScore
2.90
自引率
15.40%
发文量
216
审稿时长
3-8 weeks
期刊介绍: The aim of Pediatric Transplantation is to publish original articles of the highest quality on clinical experience and basic research in transplantation of tissues and solid organs in infants, children and adolescents. The journal seeks to disseminate the latest information widely to all individuals involved in kidney, liver, heart, lung, intestine and stem cell (bone-marrow) transplantation. In addition, the journal publishes focused reviews on topics relevant to pediatric transplantation as well as timely editorial comment on controversial issues.
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