Haruki Ayumi, Ishikawa Eiji, Katayama Kan, Ito Takayasu, Hiramoto Takuya, Fujimoto Mika, Murata Tomohiro, Ito Masaaki
Department of Cardiology and Nephrology, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie, 514-8507, Japan.
BMC Nephrol. 2018 Jul 4;19(1):162. doi: 10.1186/s12882-018-0961-y.
While the majority of adult-onset minimal change nephrotic syndrome (MCNS) is a primary or an idiopathic form of disease, it can also occur as a secondary form. Reports on the spontaneous remission of MCNS are rare since the condition is typically treated with corticosteroids. We herein describe the spontaneous remission of adult-onset MCNS in a patient who developed nephrotic syndrome after type B influenza infection.
A 50-year-old woman experienced fever, cough, malaise, and low back pain, which had persisted for 6 days before she presented to our hospital, and edema of the face and limbs, which had persisted for 5 days before her presentation. She was diagnosed with type B influenza infection and later exhibited an exacerbation of facial edema, decreased urine output, and a high level of proteinuria. She was referred to our department after the diagnosis of nephrotic syndrome. On admission, her proteinuria level was 20.88 g/gCr and her selectivity index value was 0.13. The examination of a kidney biopsy specimen obtained on the fourth day of hospitalization under a light microscope revealed minor abnormalities. An immunofluorescence showed only nonspecific granular IgM deposits in the mesangium. Electron microscopy showed extensive foot process effacement without any immune complex deposits. Based on these findings, the patient was diagnosed with MCNS. After admission, the proteinuria decreased to 0.06 g/gCr with rest and sodium restriction (6 g/day) alone; a complete remission from nephrotic syndrome was observed at approximately 2 weeks after the onset of symptoms. There have been no signs of recurrence of nephrotic syndrome in the one years since.
We experienced a rare case in which spontaneous remission of MCNS occurred within a short period of 2 weeks after influenza B infection. When patients present with nephrotic syndrome after an infection, it is necessary to consider MCNS in the differential diagnosis, which also includes post-infectious glomerulonephritis and the acute exacerbation of IgA nephropathy.
虽然大多数成人起病的微小病变肾病综合征(MCNS)是原发性或特发性疾病形式,但它也可作为继发性形式出现。由于该疾病通常用皮质类固醇治疗,关于MCNS自发缓解的报道很少。我们在此描述一名在感染乙型流感后发生肾病综合征的患者中成人起病的MCNS的自发缓解情况。
一名50岁女性在前来我院就诊前持续发热、咳嗽、全身不适和腰痛6天,面部和四肢水肿5天。她被诊断为乙型流感感染,后来出现面部水肿加重、尿量减少和高蛋白尿。在诊断为肾病综合征后,她被转诊至我们科室。入院时,她的蛋白尿水平为20.88 g/gCr,选择性指数值为0.13。住院第四天获取的肾活检标本在光学显微镜下检查显示轻微异常。免疫荧光显示仅在系膜中有非特异性颗粒状IgM沉积。电子显微镜显示广泛的足突消失,无任何免疫复合物沉积。基于这些发现,该患者被诊断为MCNS。入院后,仅通过休息和限制钠摄入(6克/天),蛋白尿降至0.06 g/gCr;在症状出现后约2周观察到肾病综合征完全缓解。自那以后的一年中,没有肾病综合征复发的迹象。
我们遇到了一例罕见病例,即MCNS在乙型流感感染后短时间内(2周内)自发缓解。当患者在感染后出现肾病综合征时,在鉴别诊断中必须考虑MCNS,鉴别诊断还包括感染后肾小球肾炎和IgA肾病的急性加重。