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首页> 外文期刊>BMC Nephrology >Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report
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Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report

机译:患有抗磷脂综合征患者患者的血浆血浆肾脏移植前:案例报告

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Background Early graft thrombosis and bleeding complications remain important causes of early graft loss following kidney transplantation in patients with antiphospholipid syndrome. Anti-β2-glycoprotein I IgG is a disease-specific antibody in patients with antiphospholipid syndrome. Although plasmapheresis is partially effective for antibody removal, the optimal treatment allowing successful transplantation in patients with antiphospholipid syndrome has not been established. This is the first report of a patient with antiphospholipid syndrome who successfully underwent living-donor kidney transplantation following prophylactic plasmapheresis for removal of anti-β2-glycoprotein I IgG. Case presentation A 37-year-old Japanese female was scheduled to undergo a living-donor kidney transplant from her mother. At age 25?years, she experienced renal vein thrombosis, was diagnosed with antiphospholipid syndrome secondary to systemic lupus erythematosus, and was subsequently treated with prednisolone and warfarin. At age 37?years, she was diagnosed with end stage kidney disease, requiring maintenance hemodialysis because of recurrent renal vein thrombosis despite taking anticoagulation therapy. The pretreatment protocol consisted of prophylactic plasmapheresis plus full anticoagulation therapy to counteract the risks of early graft thrombosis. Anticardiolipin and anti-β2-glycoprotein I IgGs were successfully removed by both double filtration plasmapheresis and plasma exchange. The allograft kidney began to function soon after transplantation. No obvious thrombotic complications were observed after transplantation, although anti-β2-glycoprotein I IgG increased to the level observed before plasmapheresis. One year after transplantation, the patient’s kidney function remains stable while receiving anticoagulation therapy as well as a maintenance immunosuppressive regimen. Conclusion Prophylactic plasmapheresis plus full anticoagulation therapy may be an effective strategy in patients with antiphospholipid syndrome undergoing living-donor kidney transplantation.
机译:背景技术早期接枝血栓形成和出血并发症仍然是肾移植患者抗磷脂综合征患者肾移植后早期接枝损失的重要原因。抗β2-糖蛋白I IgG是抗磷脂综合征患者的疾病特异性抗体。虽然血浆粉术对抗体去除部分有效,但尚未建立允许抗磷脂综合征患者成功移植的最佳治疗。这是具有抗磷脂综合征的患者的第一报告,在预防血浆术后成功接受了抗β2-糖蛋白I IgG的预防性血浆术后患者肾移植。案例介绍一位37岁的日本女性被安排从她母亲那里接受养育肾脏移植。年龄在25岁时,她经历了肾静脉血栓形成,被诊断出患有Systemic Lupus红斑狼疮的抗磷脂综合征,随后用泼尼松龙和华法林治疗。年龄在37岁时,她被诊断出患有最终阶段的肾脏疾病,需要维持血液透析,因为尽管采取抗凝治疗,但仍然需要复发肾静脉血栓形成。预防性方案包括预防性血浆术治疗加上全抗凝治疗,以抵消早期接枝血栓形成的风险。通过双过滤浆术和血浆交换成功地除去抗甘露氨素和抗β2-糖蛋白I IgG。移植后,同种异体移植的肾脏开始很快发挥作用。移植后没有观察到明显的血栓形成并发症,尽管抗β2-糖蛋白I IgG增加到血浆施术前观察到的水平。移植后一年,患者的肾功能仍然稳定,同时接受抗凝治疗以及维持免疫抑制方案。结论预防性血浆丸剂加上全抗凝治疗可能是抗磷脂综合征患者患者肾移植患者的有效策略。

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