Pediatric Urology, Department of Women's and Children's Health, Padua University Hospital, Padua, Italy.
Pediatric Surgery, Department of Women's and Children's Health, Padua University Hospital, Padua, Italy.
Pediatr Transplant. 2021 Nov;25(7):e14074. doi: 10.1111/petr.14074. Epub 2021 Jun 22.
Allograft venous thrombosis is a severe complication after kidney transplantation (KT). Early diagnosis and prompt treatment are crucial in preserving the survival of the allograft. In this study, we aimed to describe an emergent strategy for the management of acute allograft venous thrombosis.
A 4-year-old girl, weighing 13.5 kg, was diagnosed with bilateral congenital renal hypodysplasia, urogenital sinus and anorectal malformation. The patient was referred to our department for living-donor KT. Her mother was eligible as a donor, presenting a body weight ratio of 1:4.5. Thrombosis of the inferior vena cava (ICV) was also identified, without any predisposing factor for thrombophilia. KT was performed by an extraperitoneal approach without complications. Venous anastomosis required a human vascular graft sutured to the ICV, and renal artery was anastomosed to the aorta. On postoperative day (POD) 8, acute abdominal pain and hematuria led to the diagnosis of an allograft venous thrombosis. An emergent laparotomy was required to explant the allograft, followed by bench surgery. The allograft was irrigated with thrombolytic agents and lactated Ringer's solution and then after removing the venous vascular graft, it was reimplanted through vascular anastomosis with the ICV and aorta. The recovery of perfusion and function was good with diuresis since day 4 after re-surgery. At 2-year follow-up, the child presented normal allograft function with an estimated GFR of 65 ml/min/1.73 m .
According to our experience, explantation of the kidney allograft, followed by irrigation with thrombolytics in bench surgery, and reimplantation resulted in unexpected optimal outcomes in the case of allograft venous thrombosis.
同种异体移植静脉血栓形成是肾移植(KT)后的严重并发症。早期诊断和及时治疗对于保存移植物的存活至关重要。在本研究中,我们旨在描述一种用于管理急性同种异体移植静脉血栓形成的紧急策略。
一名 4 岁女孩,体重 13.5 公斤,被诊断为双侧先天性肾发育不全、尿生殖窦和肛门直肠畸形。该患者被转至我科进行活体供肾 KT。她的母亲符合供体标准,体重比为 1:4.5。还发现下腔静脉(ICV)血栓形成,没有任何血栓形成倾向的因素。KT 通过腹膜外途径进行,无并发症。静脉吻合需要将人体血管移植物缝合到 ICV 上,肾动脉吻合到主动脉上。术后第 8 天,出现急性腹痛和血尿,诊断为同种异体移植静脉血栓形成。需要紧急剖腹手术切除移植物,然后进行 bench 手术。用溶栓剂和乳酸林格氏液冲洗移植物,然后在移除静脉血管移植物后,通过与 ICV 和主动脉的血管吻合重新植入。再手术后第 4 天,开始利尿,灌注和功能恢复良好。在 2 年的随访中,患儿的移植物功能正常,估计肾小球滤过率(eGFR)为 65ml/min/1.73m。
根据我们的经验,在同种异体移植静脉血栓形成的情况下,切除肾移植物,然后在 bench 手术中用溶栓剂冲洗,再重新植入,结果出乎意料地良好。