Department of Nephrology, Japanese Red Cross Otsu Hospital, 1-1-35 Nagara, Otsu, Shiga, 520-8511, Japan.
Department of Pathology and Oncology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
CEN Case Rep. 2022 Feb;11(1):120-125. doi: 10.1007/s13730-021-00637-3. Epub 2021 Aug 28.
Although bisphosphonates are well known to cause kidney disease, there are very few published cases of focal segmental glomerulosclerosis (FSGS) following treatment with minodronate. Here we report the case of an 86-year-old woman who developed acute kidney injury and nephrotic syndrome after receiving monthly oral minodronate for 24 months. Kidney biopsy revealed cellular variant FSGS. Treatment was initiated with the discontinuation of minodronate followed by intravenous methylprednisolone pulse and prednisolone at 35 mg/day. Subsequently, the patient's renal function gradually worsened, requiring initiation of hemodialysis. However, renal function and proteinuria improved markedly and hemodialysis was withdrawn 1 month after the initiation of steroid therapy. This is, to our knowledge, the first published case of FSGS induced by long-term use of minodronate, and also the first case of cellular variant FSGS induced by bisphosphonates although collapsing variant of FSGS is commonly caused by bisphosphonates. Our study indicates that patients on bisphosphonates should be closely monitored for proteinuria and renal impairment, regardless of the type of bisphosphonate.
虽然双膦酸盐众所周知会导致肾脏疾病,但用米诺膦酸盐治疗后发生局灶节段性肾小球硬化症(FSGS)的情况非常少见。我们在此报告一例 86 岁女性患者,她在接受每月口服米诺膦酸盐治疗 24 个月后出现急性肾损伤和肾病综合征。肾活检显示为细胞型 FSGS。治疗方案为停用米诺膦酸盐,随后静脉注射甲基强的松龙脉冲和泼尼松龙 35mg/天。随后,患者的肾功能逐渐恶化,需要开始血液透析。然而,在开始类固醇治疗 1 个月后,肾功能和蛋白尿显著改善,并且停止了血液透析。据我们所知,这是首例由米诺膦酸盐长期使用引起的 FSGS 病例,也是首例由双膦酸盐引起的细胞型 FSGS 病例,尽管 FSGS 的塌陷型通常由双膦酸盐引起。我们的研究表明,无论双膦酸盐的类型如何,接受双膦酸盐治疗的患者都应密切监测蛋白尿和肾功能损害。