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节段性肝移植术后胆肠吻合口狭窄的特征与治疗

Characterization and treatment of biliary anastomotic stricture after segmental liver transplantation.

作者信息

Schindel D, Dunn S, Casas A, Billmire D, Vinocur C, Weintraub W

机构信息

Department of Pediatric Surgery, St Christopher's Hospital for Children, Philadelphia, Pennsylvania 19134, USA.

出版信息

J Pediatr Surg. 2000 Jun;35(6):940-2. doi: 10.1053/jpsu.2000.6932.

DOI:10.1053/jpsu.2000.6932
PMID:10873040
Abstract

BACKGROUND/PURPOSE: Biliary anastomotic strictures (BAS) after left lateral segment liver transplantation (LLST) may cause graft dysfunction, sepsis, and patient mortality. A review of the authors' experience was performed to better characterize the risk factors and corrective management.

METHODS

The medical records of 9 children who underwent a LLST in whom a BAS developed from 1989 to the present were reviewed retrospectively.

RESULTS

Seventy-five of 199 liver transplants (38%) at the authors' institution since 1989 have been LLST. BAS developed in 12% of these cases. BAS were diagnosed less than 12 months after transplantation in 4 children (mean, 7.5 months; range, 5 to 11 months) and greater than 12 months in 5 children (mean, 37 months; range, 14 to 72 months). Early strictures (<12 months) were associated with hepatic artery thrombosis (n = 1), and posttransplant bile leak (n = 1) and ducts from segment II and III exiting separately from the left lateral segment (n = 2). The diagnosis of BAS was heralded by episodes of liver biopsy-proven cholangitis in all patients and confirmed radiographically. Seven children underwent successful biliary exploration and revision of the hepaticojejunostomy. Two of these children ultimately required retransplantation secondary to chronic graft rejection.

CONCLUSIONS

BAS in LLST are a source of significant morbidity and should be considered in children after LLST who present with cholangitis. Surgical correction is possible in most cases.

摘要

背景/目的:左外叶肝移植(LLST)术后胆管吻合口狭窄(BAS)可导致移植物功能障碍、脓毒症和患者死亡。回顾作者的经验以更好地明确危险因素和矫正处理方法。

方法

回顾性分析1989年至今9例接受LLST且发生BAS的儿童的病历。

结果

自1989年以来,作者所在机构199例肝移植中有75例(38%)为LLST。其中12%的病例发生了BAS。4例儿童在移植后不到12个月被诊断为BAS(平均7.5个月;范围5至11个月),5例儿童在移植后超过12个月被诊断为BAS(平均37个月;范围14至72个月)。早期狭窄(<12个月)与肝动脉血栓形成(n = 1)、移植后胆漏(n = 1)以及来自第II和III段的胆管分别从左外叶引出(n = 2)有关。所有患者均经肝活检证实的胆管炎发作预示了BAS的诊断,并经影像学检查确诊。7例儿童成功接受了胆管探查和肝空肠吻合术修复。其中2例儿童最终因慢性移植物排斥反应而需要再次移植。

结论

LLST中的BAS是严重发病的一个原因,对于出现胆管炎的LLST术后儿童应予以考虑。大多数情况下手术矫正可行。

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