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小儿肝移植中的肝动脉血栓形成:血栓切除术后的移植物挽救

Hepatic artery thrombosis in pediatric liver transplantation: graft salvage after thrombectomy.

作者信息

Garcia-Gallont R, Bar-Nathan N, Shaharabani E, Yussim A, Shapira R, Zahavi I, Shapira Z, Dinari G, Mor E

机构信息

Department of Transplantation, Amedesqua Hospital, Guatemala City, Guatemala.

出版信息

Pediatr Transplant. 1999 Feb;3(1):74-8. doi: 10.1034/j.1399-3046.1999.00012.x.

Abstract

Hepatic artery thrombosis (HAT) is a devastating complication that may occur after orthotopic liver transplantation (OLT). A higher incidence has been reported in children. Salvage of the graft by thrombectomy has been suggested as an alternative to re-transplantation. In this study we report the outcome of three children who underwent thrombectomy for HAT. Between January 1992 and June 1998, 14 children (< 17 yrs of age) underwent liver transplantation. Three developed HAT (one a whole-liver graft recipient, age 17; two living-related graft recipients, ages 4 and 4.5 yr). In the first patient, thrombosis of the hepatic artery was associated with scattered areas of parenchymal necrosis on computed tomography. In the two living-related patients, HAT was found incidentally during re-exploration for bleeding (day 2 and day 10). Thrombectomy was performed in all three patients. At 18-24 months after thrombectomy, all three children had normal graft function. In the first patient, complete regeneration of the liver has been documented by computed tomography and a late asymptomatic recurrent thrombosis is suggested by absence of arterial flow on Doppler examination. The hepatic artery is patent in the two living-related recipients. One of these living-related recipients developed ischemic bile duct stricture and underwent successful percutaneous balloon dilatation. We conclude that long-term normal graft function can be achieved by thrombectomy in pediatric liver recipients with HAT, even in the presence of limited parenchymal damage.

摘要

肝动脉血栓形成(HAT)是原位肝移植(OLT)后可能发生的一种严重并发症。据报道,其在儿童中的发生率较高。有人建议通过血栓切除术挽救移植肝,作为再次移植的替代方案。在本研究中,我们报告了3例因HAT接受血栓切除术的儿童的治疗结果。1992年1月至1998年6月期间,14例(年龄<17岁)儿童接受了肝移植。3例发生了HAT(1例为全肝移植受者,年龄17岁;2例为活体亲属供肝移植受者,年龄分别为4岁和4.5岁)。在第1例患者中,肝动脉血栓形成与计算机断层扫描显示的实质坏死散在区域相关。在2例活体亲属供肝患者中,HAT是在因出血再次探查时(第2天和第10天)偶然发现的。3例患者均接受了血栓切除术。血栓切除术后18 - 24个月时,3例儿童的移植肝功能均正常。在第1例患者中,计算机断层扫描已证实肝脏完全再生,而多普勒检查显示无动脉血流提示有晚期无症状复发性血栓形成。2例活体亲属供肝受者的肝动脉通畅。其中1例活体亲属供肝受者发生了缺血性胆管狭窄,并成功接受了经皮气囊扩张术。我们得出结论,即使存在有限的实质损伤,对于患有HAT的小儿肝移植受者,通过血栓切除术也可实现长期正常的移植肝功能。

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