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Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
A child with systemic onset juvenile idiopathic arthritis and nephrotic syndrome
Jyoti S Singhal1, Nivedita Pande1, Jyoti Sharma2
1King Edward Memorial Hospital, Pune, India.
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.
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