Rapid and persistent reduction of proteinuria following plasma exchange in a case of steroid-resistant focal segmental glomerulosclerosis.

E. Ishii, Y. Ando, K. Tamba, Y. Masunaga, E. Kusano, Y. Asano
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引用次数: 1

Abstract

We report on the case of a 45 year old male with focal segmental glomerulosclerosis (FSGS) in whom steroid-resistant proteinuria was reduced rapidly by plasma exchange. In 1994, he was admitted to our hospital because of massive proteinuria of several years' duration. Renal biopsy confirmed the diagnosis of FSGS. Proteinuria was suppressed partially with the use of dipyridamole. Though oral prednisolone (PSL, 30 mg/day) was effective initially, relapse occurred during PSL tapering. Doses of PSL up to 30 mg/day or additional mizoribine were ineffective. The patient was readmitted for a trial of plasma exchange in April 2000. Four sessions of plasma exchange with albumin replacement over 2 weeks immediately reduced the proteinuria from 3.2 g/day to 0.6 g/day without any change in medication. After discharge, proteinuria remained suppressed for more than 6 months despite a reduction of PSL dose to 15 mg. The rapid and long lasting effect of plasma exchange in the present case argues for the role of a putative circulatory factor in the pathogenesis of proteinuria in FSGS.
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类固醇抵抗局灶节段性肾小球硬化1例血浆置换后蛋白尿快速持续减少。
我们报告一例45岁男性局灶节段性肾小球硬化(FSGS)患者,其类固醇抵抗性蛋白尿通过血浆交换迅速减少。1994年因持续数年的大量蛋白尿入住我院。肾活检证实了FSGS的诊断。使用双嘧达莫可部分抑制蛋白尿。虽然口服强的松龙(PSL, 30mg /天)最初有效,但在PSL逐渐减少时发生复发。PSL的剂量高达30毫克/天或额外的米佐利滨无效。患者于2000年4月再次入院接受血浆置换试验。在2周内进行4次血浆置换和白蛋白替代,可立即将蛋白尿从3.2 g/天减少到0.6 g/天,而药物没有任何变化。出院后,尽管PSL剂量减少至15mg,但蛋白尿仍保持抑制超过6个月。在本病例中,血浆交换的快速和持久的效果证明了一种假定的循环因子在FSGS蛋白尿发病机制中的作用。
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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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