Sahin Hatice, Gok Oguz Ebru, Akoglu Hadim, Atilgan Gokhan, Ulusal Okyay Gulay, Karaveli Gursoy Guner, Kip Teymur Tugba, Ertoy Dilek, Canbakan Basol, Ayli Mehmet Deniz
Department of Nephrology, Diskapi Yildirim Beyazit Education and Research Hospital, Ankara, Turkey.
Iran J Kidney Dis. 2018 Oct;12(5):315-318.
Two-thirds of complement C3 glomerulopathy (C3G) recur after transplantation and commonly cause graft loss. There is not a standard treatment protocol for these cases. We present a kidney transplant patient with recurrent C3G who was successfully treated with eculizumab. Nephrotic proteinuria and hematuria occurred and creatinine levels increased after transplantation. A graft biopsy revealed recurrent C3G. The patient was administered 250 mg pulse methylprednisolone for 3 days and had 9 sessions of plasmapheresis. Since elevated creatinine levels and proteinuria persisted, eculizumab was instituted. A complete remission was observed after 9-month maintenance eculizumab treatment. Eculizumab may be a potentially effective option in kidney transplant patients with recurrent C3G unresponsive to other treatment modalities.
三分之二的补体C3肾小球病(C3G)在移植后复发,且通常导致移植肾失功。对于这些病例尚无标准的治疗方案。我们报告一例复发性C3G肾移植患者,其接受依库珠单抗治疗获得成功。该患者移植后出现肾病性蛋白尿和血尿,肌酐水平升高。移植肾活检显示C3G复发。患者接受了3天的250mg甲泼尼龙冲击治疗,并进行了9次血浆置换。由于肌酐水平升高和蛋白尿持续存在,遂开始使用依库珠单抗治疗。依库珠单抗维持治疗9个月后观察到完全缓解。对于其他治疗方式无反应的复发性C3G肾移植患者,依库珠单抗可能是一种潜在有效的选择。