Chidhood Nephrotic Syndrome in Ilorin.
Abstract
Summary: A cohort of 17 children (12M:5F), aged 3-16 years, with nephrotic syndrome seen at the University of Ilorin Teaching Hospital, Ilorin, between Janu ary 1995 and December 1998 were studied. Renal biopsies were performed in eight patients. Five (63 per cent) of the biopsies showed focal mesangial proliferative glomerulonephritis while one each showed minimal change, membranoproliferative, and mesangial proliferative glomerulonephritis on light microscopy. Only three (17.6 per cent) of the 17 patients were steroid responsive, while six (35 per cent) were steroid resistant. The predominant histologi cal finding in the steroid resistant cases was focal mesangial proliferative le rate was 12 per cent from two deaths. The histopathological findings in the two patients who died of end-stage renal disease, consisted of minimal change lesion and membranoproliferative glomerulonephritis, respectively.
Downloads
Published
Issue
Section
License
This is an open-access journal, and articles are distributed under the terms of the Creative Commons Attribution 4.0 License, which allows others to remix, transform, and build upon the work even, commercially, as long as appropriate credit is given to the author, and the new creations are licensed under identical terms