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一名患有全身型幼年特发性关节炎和肾病综合征的儿童。

A child with systemic onset juvenile idiopathic arthritis and nephrotic syndrome.

作者信息

Singhal Jyoti S, Pande Nivedita, Sharma Jyoti

机构信息

King Edward Memorial Hospital, Pune, India.

出版信息

Pediatr Nephrol. 2025 Feb;40(2):381-383. doi: 10.1007/s00467-024-06495-2. Epub 2024 Sep 9.

Abstract

INTRODUCTION

Amyloidosis of the kidney is a rare complication in children with juvenile idiopathic arthritis (JIA), more commonly seen with systemic onset juvenile idiopathic arthritis (SOJIA). It usually presents with asymptomatic proteinuria.

CASE REPORT

An 11.5-year-old boy with onset of SOJIA at 6 years of age came to our clinic with anasarca. Urinalysis and serum albumin suggested a diagnosis of nephrotic syndrome (NS) and kidney biopsy confirmed amyloidosis deposits. Treatment with injection tocilizumab was initiated. The proteinuria has decreased, and kidney functions are normal.

CONCLUSION

Children with SOJIA should be monitored for proteinuria so that they can be offered timely appropriate therapy.

摘要

引言

肾淀粉样变性是幼年特发性关节炎(JIA)患儿中一种罕见的并发症,在全身型幼年特发性关节炎(SOJIA)中更为常见。它通常表现为无症状蛋白尿。

病例报告

一名11.5岁男孩,6岁起病,患全身型幼年特发性关节炎,因全身水肿前来我院就诊。尿液分析和血清白蛋白提示诊断为肾病综合征(NS),肾脏活检证实有淀粉样变性沉积物。开始使用托珠单抗注射治疗。蛋白尿已减少,肾功能正常。

结论

应监测全身型幼年特发性关节炎患儿的蛋白尿情况,以便能及时给予适当治疗。

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