Korean Journal of Nephrology 2010;29(2):292-295.
Rituximab and Plasmapheresis for Post-transplant Recurrence of FSGS
Ju-Yeon Nam, M.D.1, An-Sook Choi, M.D.1, Su-Jin Kim, M.D.1, Byoung-Hoon Ji, M.D.1, Joon-Suk Oh, M.D.1, Young-Ki Son, M.D.1, Yong-Hun Sin, M.D.1, Joong-Kyung Kim, M.D.1 and Yong-Jin Kim, M.D.2
Division of Nephrology, Department of Internal Medicine Bong Seng Memorial Hospital, Busan, Korea1
Department of Pathology, Yeung Nam University Hospital2
증례 : 신장 이식 후 재발한 국소성 분절성 사구체 경화증 치료로 사용한 Rituximab과 혈장교환술 plasmapheresis 1예
남주연1, 최안숙1, 김수진1, 지병훈1, 오준석1, 손영기1, 신용훈1, 김중경1, 김용진2
김원묵 기념 봉생병원 내과학교실1 , 영남대학교 병리학교실2
Abstract
Focal segmental glomerular sclerosis (FSGS) is known to recur in 20-40% of the renal allografts with graft loss in about half of these cases. We report a successful treatment of a recurrent FSGS after kidney transplantation with rituximab and plasmapheresis. An 16-year-old patient whose primary kidney disease was FSGS developed recurrence of proteinuria after living donor kidney transplantation despite preemptive plasmapheresis and one dose of rituximab (375 mg/m2). After kidney transplantation, nephritic range proteinuria was detected. Kidney biopsy was done and showed recurrent FSGS. She undergone 11 times of plasmapheresis in the first 4 week post transplantation. In addition, she received additional one dose of rituximab (375 mg/m2) on day 14. Proteinuria was decreased below nephritic range at 37 day. Ten months later, proteinuria was at 30 mg/day with excellent graft function. No significant adverse events related to rituximab or plasmapheresis were observed. Rituximab with plasmapheresis may be another option for recurrent FSGS after kidney transplantation.
Key Words: Focal segmental glomerulosclerosis, Rituximab, Kidney transplantation
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