Maeda Ryo, Kawasaki Yukihiko, Suzuki Shigeo, Ohara Shinichiro, Kazuhide Suyama, Hosoya Mitsuaki
Department of Pediatrics, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima, Fukushima, 960-1295, Japan.
Department of Pediatrics, Ohara General Hospital, 6-11 Omachi, Fukushima, Fukushima, 960-8041, Japan.
CEN Case Rep. 2018 May;7(1):13-16. doi: 10.1007/s13730-017-0282-1. Epub 2017 Nov 15.
Minor infections, allergies, insect bites, and bee stings are commonly reported causes of nephrotic syndrome (NS). Herein, we report, to the best of our knowledge, the first case of NS relapse due to Kawasaki disease (KD). An 8-year-old boy presented with high fever of 4-day duration. He had developed steroid-dependent NS at the age of 4 years and remained in remission after steroid and mizonbin therapy. Renal biopsy, performed at the age of four, showed minimal change (MC) disease. Upon examination, the patient fulfilled 5 of 6 criteria for KD under the Japanese diagnostic guidelines, with positive proteinuria. He was diagnosed with NS relapse caused by KD. Proteinuria resolved after treatment with intravenous immunoglobulin and cyclosporine A. We present the case of an 8-year-old boy, whose NS relapsed due to KD. To the best of our knowledge, this is the first case report. It is necessary to recognize that KD can trigger relapse of MCNS.
轻微感染、过敏、昆虫叮咬和蜜蜂蜇伤是肾病综合征(NS)常见的报道病因。在此,据我们所知,我们报告了首例因川崎病(KD)导致肾病综合征复发的病例。一名8岁男孩出现持续4天的高热。他在4岁时患上激素依赖型肾病综合征,在接受激素和咪唑立宾治疗后病情缓解。4岁时进行的肾活检显示为微小病变(MC)病。经检查,该患者符合日本诊断指南中川崎病6项标准中的5项,伴有蛋白尿。他被诊断为川崎病导致的肾病综合征复发。静脉注射免疫球蛋白和环孢素A治疗后蛋白尿消失。我们报告了一名8岁男孩的病例,其肾病综合征因川崎病复发。据我们所知,这是首例病例报告。有必要认识到川崎病可引发微小病变肾病综合征复发。