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Epidemiology of renal disease in children in the region of southern Croatia: a 10-year review of regional biopsy detabases (CROSBI ID 133678)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Bazina, Mirna ; Glavina-Durdov, Meri ; Ščukanec-Špolar, Mira ; Bazina, Antonela ; Vukojević, Katarina ; Ljutić, Dragan ; Saraga, Marijan Epidemiology of renal disease in children in the region of southern Croatia: a 10-year review of regional biopsy detabases // Medical science monitor, 13 (2007), 4; 172-172

Podaci o odgovornosti

Bazina, Mirna ; Glavina-Durdov, Meri ; Ščukanec-Špolar, Mira ; Bazina, Antonela ; Vukojević, Katarina ; Ljutić, Dragan ; Saraga, Marijan

engleski

Epidemiology of renal disease in children in the region of southern Croatia: a 10-year review of regional biopsy detabases

Epidemiological data on some renal diseases in children are available from world national registries of renal biopsies. However, there is no published study of biopsy-proven childhood glomerulonephritis in Croatia. This report is the first review of pathohistological data covering a pediatric population over a 10-year period in the Croatian region of Dalmatia. A retrospective study was done on all renal biopsies from 65 children under 18 years of age received by the Clinical Hospital Split between 1995 and 2005. The histopathological findings were reviewed to determine the pattern of biopsy-proven glomerulonephritis. Indications for renal biopsy and clinico-pathological correlations were studied. Data on serum creatinine concentration, 24-h proteinuria, hematuria, clinical diagnosis, pathohistological diagnosis, and post-biopsy complications were collected. The main indications for biopsy were nephrotic syndrome (41.5%), hematuria with proteinuria (23.1%), and isolated hematuria (12.3%). The most frequent renal diseases in decreasing order were mesangioproliferative glomerulonephritis (27.7%), IgA nephropathy (13.8%), and Henoch-Schönlein nephritis (10.8%). Tubulointerstitial nephritis, focal segmental glomerulosclerosis, and endoproliferative glomerulonephritis each accounted for 6.2%. Alport syndrome, fibrillary glomerulonephritis, and minimal change diseases were each found in 4.6% of cases. Other forms of glomerulonephritis were rarely found. The present data represent the basis for a future Croatian Registry of Renal Biopsies and are an important contribution to the epidemiology of renal diseases in south-eastern Europe. Three cases of fibrillary glomerulonephritis in children with steroid-dependent nephrotic syndrome, not reported in other countries’ registries, were also found. The importance of ultrastructural analysis of biopsy specimens is emphasized.

childern; epidemiology; fibrillary glomerulonephritis; registry; renal biopsy

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Podaci o izdanju

13 (4)

2007.

172-172

objavljeno

1234-1010

Povezanost rada

Temeljne medicinske znanosti, Kliničke medicinske znanosti

Indeksiranost