| Objective To study the feature of clinic, pathology and prognosis inchildren with steroid-resistant nephritic syndrome(SRNS).Methods Children with SRNS hospitalized in Division ofNephrology and Immunology of our hospital from January2003toDecember2012were analyzed retrospectively in clinic, pathology andprognosis.Results162patients were investigated,which accounted for10.8%of children with Primary nephritic syndrome(PNS),and the mean age ofonset was6.9±3.8years.(1)Renal biopsy was performed in132patients,of them60showed mesangial proliferative glomerulonephritis(MsPGN),30showed focal segmental glomerulosclerosis(FSGS),19showed minimalchange disease(MCD),8showed membranoproliferativeglomerulonephritis (MPGN),5showed membranous nephropathy (MN),1showed proliferative sclerosis glomerulonephritis (PSGN). Patients with non minimal change disease (non-MCD) had a signifinant prevalence ofhematuria. The distribution of pathologic type between age groups andclinical classification was signifinantly different respectively (P<0.05).(2)132patients were followed up,of them58was in complete remission,26was in partial remission,15was not in remission,8was dead, and themean time for complete remission was15months(3~84).Prognosiscorrelated with pathologic type(P<0.01)。Conclusion (1)There was a preponderance of non-MCD in childrenwith SRNS,and with MsPGN and FSGS being the major pathologic type.Hematuria was a predictor of glucocorticoid resistance.(2)Children withSRNS had a long time proteinuria and poor prognosis. FSGS had a poorprognosis compared to those with MsPGN. |