A case of nephrotic syndrome due to lupus nephritis which was controlled with low-density lipoprotein apheresis.

Yuji Kamijo, Yoko Kaneko, Toru Ichikawa, Nobuhiko Kobayashi, Takayuki Koyama, Tetsuji Kakegawa, Hiroshi Kamijo, Keiichi Kono, Satoshi Minami, Naoki Tanaka, Hideo Arakura, Masayuki Hirata, Makoto Higuchi, Kendo Kiyosawa, Kazuhiko Hora
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引用次数: 10

Abstract

Our report discusses a 29 year old female patient with nephrotic syndrome due to lupus nephritis, biopsy-proven World Health Organization classification Types IVb and V that was controlled with low-density lipoprotein (LDL) apheresis. She was initially treated with steroid therapy, including methylprednisolone pulse therapy, and the serological activity of her systemic lupus erythematosus was suppressed. However, her nephrotic state, accompanied by severe hyperlipidemia, persisted despite the steroid therapy. Since we could not obtain her consent to administer immunosuppressants such as cyclophosphamide, we tried to treat her using LDL apheresis (LDL-A). We found that her urine protein excretion, hyperlipidemia, hypoalbuminemia, and renal function improved following the initiation of LDL-A. This suggests that LDL-A may be an effective therapy for nephrotic syndrome due to lupus nephritis through short-term amelioration of hyperlipidemia.

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狼疮性肾炎肾病综合征应用低密度脂蛋白分离治疗1例。
我们的报告讨论了一例29岁女性狼疮肾炎肾病综合征患者,活检证实为世界卫生组织分类IVb和V型,并采用低密度脂蛋白(LDL)采血控制。她最初接受类固醇治疗,包括甲基强的松龙脉冲治疗,她的系统性红斑狼疮血清学活性被抑制。然而,尽管类固醇治疗,她的肾病状态,并伴有严重的高脂血症,持续存在。由于我们无法获得她同意使用免疫抑制剂如环磷酰胺,我们尝试使用低密度脂蛋白单采(LDL- a)治疗她。我们发现她的尿蛋白排泄、高脂血症、低白蛋白血症和肾功能在开始LDL-A治疗后得到改善。提示LDL-A可能通过短期改善高脂血症而有效治疗狼疮性肾炎所致肾病综合征。
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Presidential Address: PRESIDENTIAL ADDRESS Fluctuations in the peripheral blood leukocyte and platelet counts in leukocytapheresis in healthy volunteers. Mobilization factors of peripheral blood stem cells in healthy donors. Cytokine removal by plasma exchange with continuous hemodiafiltration in critically ill patients. In vitro evaluation of newly developed adsorbent for selective removal of glycosylated low-density lipoprotein.
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