Ishida Ryo, Shimizu Akira, Kitani Takashi, Nakata Mayumi, Ota Noriyoshi, Kado Hiroshi, Shiotsu Yayoi, Ishida Mami, Tamagaki Keiichi
Division of Nephrology, Department of Medicine, Kyoto Prefecture University of Medicine, Japan.
Intern Med. 2016;55(19):2837-2842. doi: 10.2169/internalmedicine.55.7011. Epub 2016 Oct 1.
A 30-year-old woman with myelodysplastic syndrome underwent allogeneic hematopoietic stem cell transplantation (HSCT) derived from her HLA-matched sister six years previously. She received preconditioning total body irradiation with renal shielding and was subsequently administered cyclosporin A (CyA) as prophylaxis against graft-versus-host disease (GVHD). Four months after HSCT, asymptomatic proteinuria and glomerular hematuria developed during CyA tapering without obvious extrarenal involvements of GVHD, and persisted for six years. A renal biopsy revealed endothelial injury in the glomeruli, and the deposition of C4d was detected diffusely on glomerular capillaries and focally on peritubular capillaries, suggesting that nephropathy involved antibody- or complement-associated immune reactions.
一名30岁的骨髓增生异常综合征女性患者,六年前接受了来自其HLA配型相合妹妹的异基因造血干细胞移植(HSCT)。她接受了肾脏屏蔽的全身预处理照射,随后给予环孢素A(CyA)预防移植物抗宿主病(GVHD)。HSCT后四个月,在CyA减量过程中出现无症状蛋白尿和肾小球血尿,无明显GVHD肾外累及,并持续了六年。肾活检显示肾小球内皮损伤,C4d在肾小球毛细血管弥漫性沉积,在肾小管周围毛细血管局灶性沉积,提示肾病涉及抗体或补体相关的免疫反应。