Japanese journal of pediatric nephrology
Online ISSN : 1881-3933
Print ISSN : 0915-2245
ISSN-L : 0915-2245
Case Reports
A case of nephrotic syndrome showing collaptic glomeruli and tubulointerstitial changes
Hironobu EguchiBunshiro AkikusaRyugo HiramotoShinsuke Matsumoto
Author information
JOURNAL FREE ACCESS

2012 Volume 25 Issue 2 Pages 153-156

Details
Abstract

We experienced a 10-year-old boy with steroid-resistant nephrotic syndrome accompanied with collaptic glomeruli and tubulointerstitial change such as tubules filled with urinary casts, interstitial fibrosis and inflammatory cells in interstitium. In the beginning, it was greatly difficult to wean this patient from full dosage of prednisolone. The introduction of cyclosporine treatment enabled maintaining the remission and weaning steroid. The second renal biopsy was performed one year after combination therapy including cyclosporine treatment, which revealed no remarkable findings. The patient was finally diagnosed with minimal change nephrotic syndrome based on these results, and then prednisolone was stopped. To date, the single use of cyclosporine has been successfully keeping the remission.

Content from these authors
© 2012 The Japanese Society for Pediatric Nephrology
Previous article Next article
feedback
Top