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异基因骨髓移植后供体淋巴细胞输注相关的膜性肾病。

Membranous nephropathy associated with donor lymphocyte infusion following allogeneic bone marrow transplantation.

作者信息

Miyazaki Yasuhiko, Mori Yasukiyo, Kishimoto Noriko, Matsumoto Noriaki, Zen Katsuhiro, Amakawa Ryuichi, Kishimoto Yuji, Fukuhara Shirou

机构信息

First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

出版信息

Int J Hematol. 2003 Oct;78(3):262-5. doi: 10.1007/BF02983805.

Abstract

Nephrotic syndrome after hematopoietic stem cell transplantation (HSCT) followed by donor lymphocyte infusion (DLI) has never been described. We report the case of a myelodysplastic syndrome (MDS) patient who developed nephrotic syndrome with membranous nephropathy 18 months after allogeneic HSCT and 4 months after DLI. A 50-year-old woman with MDS underwent allogeneic bone marrow transplantation from her HLA-matched brother. MDS relapsed 55 days after transplantation, donor lymphocytes were infused as adoptive immunotherapy, and complete remission was achieved. Four months after the third DLI, the patient developed nephrotic syndrome with proteinuria up to 9 g/day. Renal biopsy revealed granular deposits of immunoglobulin G along the glomerular basement membrane, and subepithelial electron-dense deposits. A diagnosis of membranous nephropathy was made. For maintenance of the immunotherapeutic effect of DLI, minimum doses of immunosuppressive therapy for decreasing proteinuria were administered, and improvement of nephrotic syndrome and persistent complete remission of MDS were achieved.

摘要

造血干细胞移植(HSCT)后接受供体淋巴细胞输注(DLI)并发肾病综合征的情况此前从未有过报道。我们报告了一例骨髓增生异常综合征(MDS)患者,该患者在异基因HSCT后18个月及DLI后4个月出现了伴有膜性肾病的肾病综合征。一名50岁的MDS女性患者接受了来自其HLA配型相合的兄弟的异基因骨髓移植。移植后55天MDS复发,作为过继性免疫疗法输注了供体淋巴细胞,并实现了完全缓解。在第三次DLI后4个月,患者出现了肾病综合征,蛋白尿高达9g/天。肾活检显示免疫球蛋白G沿肾小球基底膜呈颗粒状沉积,以及上皮下电子致密沉积物。诊断为膜性肾病。为维持DLI的免疫治疗效果,给予了最低剂量的免疫抑制治疗以减少蛋白尿,实现了肾病综合征的改善以及MDS的持续完全缓解。

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