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小儿活体肝移植治疗布加综合征:应用冷冻保存肺静脉移植物重建肝后下腔静脉 1 例报告。

Pediatric living donor liver transplant for Budd-Chiari syndrome using a cryopreserved pulmonary vein graft for retro-hepatic vena cava reconstruction: A case report.

机构信息

Department of General Surgery, Université de Montréal, Montréal, Québec, Canada.

Department of Pediatric Surgery, Centre hospitalier universitaire Sainte-Justine, Montréal, Québec, Canada.

出版信息

Pediatr Transplant. 2024 Feb;28(1):e14674. doi: 10.1111/petr.14674. Epub 2023 Dec 6.

DOI:10.1111/petr.14674
PMID:38054589
Abstract

INTRODUCTION

In pediatric patients with Budd-Chiari syndrome (BCS), living donor liver transplantation (LDLT) raises substantial challenges regarding IVC reconstruction.

CASE PRESENTATION

We present a case of an 8-year-old girl with BCS caused by myeloproliferative syndrome with JAK2 V617F mutation. She had a complete thrombosis of the inferior vena cava (IVC) with multiple collaterals, developing a Budd-Chiari syndrome. She underwent LDLT with IVC reconstruction with a cryopreserved pulmonary vein graft obtained from a provincial biobank. The living donor underwent a laparoscopic-assisted left lateral hepatectomy. The reconstruction of the vena cava took place on the back table and the liver was implanted en bloc with the reconstructed IVC in the recipient. Anticoagulation was immediately restarted after the surgery because of her pro-thrombotic state. Her postoperative course was complicated by a biliary anastomotic leak and an infected biloma. The patient recovered progressively and remained well on outpatient clinic follow-up 32 weeks after the procedure.

CONCLUSION

IVC reconstruction using a cryopreserved pulmonary vein graft is a valid option during LDLT for pediatric patients with BCS where reconstruction of the IVC entails considerable challenges. Early referral to a pediatric liver transplant facility with a multidisciplinary team is also important in the management of pediatric patients with BCS.

摘要

介绍

在小儿布加综合征(BCS)患者中,活体肝移植(LDLT)在腔静脉重建方面带来了巨大的挑战。

病例介绍

我们报告了 1 例由 JAK2 V617F 突变引起的骨髓增殖性综合征导致的小儿 BCS 病例。该患者下腔静脉(IVC)完全血栓形成,伴有多处侧支循环形成布加综合征。她接受了 LDLT 治疗,并使用从省级生物库获得的冷冻保存肺静脉移植物进行 IVC 重建。供体接受了腹腔镜辅助左外侧肝切除术。腔静脉重建在手术台上进行,肝脏与重建的 IVC 一起整块植入受者体内。由于她存在血栓前状态,手术后立即重新开始抗凝治疗。术后,患者出现胆肠吻合口漏和感染性胆汁瘤,病情复杂。患者逐渐恢复,在手术后 32 周的门诊随访中情况良好。

结论

在小儿 BCS 患者的 LDLT 中,使用冷冻保存肺静脉移植物进行 IVC 重建是一种有效的选择,因为 IVC 的重建具有相当大的挑战性。在小儿 BCS 的管理中,早期向具有多学科团队的小儿肝移植中心转诊也很重要。

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