Literature DB >> 18044469

[Clinical and histopathological characteristics of biopsy-proven renal diseases in Croatia].

Danica Batinić1, Mira Sćukanec-Spoljar, Danko Milosević, Mirna Subat-Dezulović, Marjan Saraga, Jasna Delmis, Zvonimir Puretić, Andrea Cvitkovic-Kuzmić, Natasa Skitarelić, Marija Spajic, Ljiljana Nizić, Kristina Vrljicak, Maja Matković, Hrvoje Kniewald, Danko Batinić, Lana Grković, Irena Borojević, Sanja Flajsman, Durdica Kosuljandić-Vukić, Semsa Marić, Danica Ljubanović.   

Abstract

There is little data on the spectrum of renal diseases in children in Croatia. The Croatian Society for Pediatric Nephrology has established the Registry of Biopsy-Proven Renal Diseases in an attempt to address this issue nationwide. Here we report preliminary results of a retrospective analysis of clinical and histopathological data of 565 children aged < or =17 years presenting to 9 hospitals in Croatia from 1991 to 2004, in whom kidney biopsy was performed. The most common indication for renal biopsy was nephrotic syndrome (39.1%), followed by asymptomatic proteinuria/hematuria (22.0%) and acute nephritic syndrome (17.0%). All biopsies were analysed by light-, immunofluorescent and electron microscopy. The majority of children, 552 out of 565 (92.4%), had glomerulonephritis (GN). Tubulointerstitial nephritis was found in 16 (2.8%), congenital renal parenchyma anomalies in 14 (2.5%) and vascular disease in 11 (1.9%) cases. One (0.2%) child had sarcoidosis with nephrocalcinosis. The sample was non-diagnostic in 1 (0.2%) case. Among children with GN, primary GN accounted for 70.9%, secondary GN for 16.1% and hereditary GN for 13.0% cases. The most frequent primary GN forms were focal segmental glomerulosclerosis (FSGS) (24.6%), mesangial proliferative glomerulonephritis (MEPGN) (19.2%) and IgA nephropathy (18.1%). Acute GN in resolution was found in 11.1% and minimal changes GN in 6.8% of cases. Most children with secondary GN had nephritis of Henoch-Schönlein purpura (HSP) (54.7%) and nephritis of systemic lupus erythematosus (SLE) (40.5%), while among hereditary GN Alport syndrome was most common (80.9%). In the group of children with primary GN who presented with nephrotic syndrome, most common forms were FSGS (38.5%) and MEPGN (24.0%). Minimal changes GN accounted for only 10.9% of cases. IgA nephropathy, primary or related to HSP (20.0%), FSGS (16.1%), MEPGN (12.6%) and Alport syndrome (9.7%) were the most common biopsy-proven renal diseases in Croatian children. The analysis provided data on the frequency of histological renal lesions in children in Croatia. The higher frequency of FSGS and MEPGN among Croatian children in comparison with other countries deserves further evaluation.

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Year:  2007        PMID: 18044469

Source DB:  PubMed          Journal:  Acta Med Croatica        ISSN: 1330-0164


  6 in total

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2.  The incidence of the nephrotic syndrome in childhood in Germany.

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3.  Clinical course & management of childhood nephrotic syndrome in Germany: a large epidemiological ESPED study.

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4.  Epidemiology of 10-year paediatric renal biopsies in the region of southern Croatia.

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5.  Clinical correlation and prognostic significance of immunofluorescence in renal biopsies of patients having Glomerulonephritis.

Authors:  Fauzia Zafar; M Faisal Mehar; Afsheen Asghar Khan; Rabia Saleem Safdar
Journal:  Pak J Med Sci       Date:  2021 Jan-Feb       Impact factor: 1.088

6.  Focal Segmental Glomerulosclerosis in Paediatric Population of South Punjab Pakistan: A Tertiary Care Hospital Experience.

Authors:  Rabia Saleem Safdar; M Faisal Mehar; Afsheen Asghar Khan; Nusrat Buzdar
Journal:  Pak J Med Sci       Date:  2021 Mar-Apr       Impact factor: 1.088

  6 in total

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