Ikeda Kensuke, Okamoto Tomoko, Yamamura Takashi, Ohsawa Isao, Furutera Rie, Murata Miho
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry.
Rinsho Shinkeigaku. 2013;53(1):19-23. doi: 10.5692/clinicalneurol.53.19.
A 59-year-old man (case 1) with multiple sclerosis (MS) presented with shortness of breath and general fatigue. He had been treated using interferon β-1b (IFNβ-1b) since he was 51 years of age. Laboratory test results showed hypoproteinemia and hypoalbuminemia, proteinuria, and absence of hematuria. He was diagnosed with nephrotic syndrome, and the administration of IFNβ-1b was stopped. Percutaneous renal biopsy was performed, and the histology revealed membranous nephropathy. A 33-year-old woman (case 2) with MS, who had been treated using IFNβ-1b for 7 years, was diagnosed with proteinuria during a medical checkup. She was referred to a nephrologist and was found to have hypoalbuminemia and proteinuria. A diagnosis of nephrotic syndrome was made, and IFNβ-1b therapy was stopped. The patient underwent percutaneous renal biopsy, and the histology revealed membranous nephropathy. Both patients were treated using intravenous methylprednisolone followed by oral prednisolone. Case 1 was administered ciclosporin orally, and his clinical symptoms and laboratory test results improved at first, but his laboratory test results subsequently showed recurrence of proteinuria. Case 2 was administered mizoribine orally, resulting in improvement in clinical symptoms and laboratory test results. Case 2 showed relapse of multiple sclerosis, but the symptoms were mild and were alleviated after steroid therapy. IFNβ therapy has several complications including nephropathy. Previously, several cases of nephrotic syndrome associated with IFNβ within 2 years of therapy were reported, but drug-induced nephropathy could appear after several years of the therapy as our cases. We should pay attention to nephrotic syndrome under using long-term IFNβ.
一名59岁患有多发性硬化症(MS)的男性(病例1)出现呼吸急促和全身乏力。他自51岁起就开始使用β-1b干扰素(IFNβ-1b)进行治疗。实验室检查结果显示低蛋白血症、低白蛋白血症、蛋白尿,且无血尿。他被诊断为肾病综合征,随后停用了IFNβ-1b。进行了经皮肾活检,组织学检查显示为膜性肾病。一名33岁患有MS的女性(病例2),使用IFNβ-1b治疗7年,在一次体检中被诊断出蛋白尿。她被转诊至肾病科医生处,发现有低白蛋白血症和蛋白尿。诊断为肾病综合征,停用了IFNβ-1b治疗。患者接受了经皮肾活检,组织学检查显示为膜性肾病。两名患者均先接受静脉注射甲泼尼龙治疗,随后口服泼尼松龙。病例1口服环孢素,其临床症状和实验室检查结果起初有所改善,但随后实验室检查结果显示蛋白尿复发。病例2口服咪唑立宾,临床症状和实验室检查结果均有所改善。病例2出现了多发性硬化症复发,但症状较轻,经类固醇治疗后得到缓解。IFNβ治疗有多种并发症,包括肾病。此前,有报道称在治疗2年内出现了几例与IFNβ相关的肾病综合征,但正如我们的病例所示,药物性肾病可能在治疗数年之后出现。我们在长期使用IFNβ时应注意肾病综合征。