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Clinicopathological features of paediatric renal biopsies in Shanghai over a 31 year period.

Authors :
ZHENG, YIBING
XU, HONG
ZHOU, LIJUN
CAO, QI
SUN, LI
SHEN, QIAN
GUO, WEI
FANG, XIAOYAN
LIU, HAIMEI
ZHANG, JUN
RAO, JIA
CHEN, JIN
Source :
Nephrology. Mar2012, Vol. 17 Issue 3, p274-277. 4p. 1 Chart.
Publication Year :
2012

Abstract

ABSTRACT: Aim: To identify the variations in paediatric renal biopsy pathology and clinicopathological features during the past 31 years. Methods: A retrospective analysis of paediatric renal biopsies performed at a single institution in Shanghai from January 1979 to December 2009 was conducted. Results: The major pathologies included minor glomerular abnormalities (MGA, 26.1%), IgA nephropathy (IgAN, 17%) and mesangial proliferative glomerulonephritis (MsPGN) without IgA deposition (11.3%). The major clinical presentations included nephrotic syndrome (NS, 39.4%), haematuria with proteinuria (24.4%) and persistent microscopic haematuria (15.1%). MGA accounted for 46.9% of the cases in NS. IgAN and HSN accounted for 24% and 28.9% of patients with concomitant haematuria and proteinuria, and thin basement membrane nephropathy accounted for 51.2% of cases with persistent microscopic haematuria. The frequency of IgAN (78.6%) was much higher than that of TBMN (29.0%) in patients with persistent microscopic haematuria with abnormal urinary albumin. Conclusion: Minor glomerular abnormalities and IgAN were the major renal diseases in our study population, and the focus of our paediatric nephrologists. The high proportion of TBMN suggested that there should be limited use of renal biopsy for patients with persistent microscopic haematuria and renal biopsy should be performed in the presence of proteinuria or abnormal levels of urinary albumin. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13205358
Volume :
17
Issue :
3
Database :
Academic Search Index
Journal :
Nephrology
Publication Type :
Academic Journal
Accession number :
71933917
Full Text :
https://doi.org/10.1111/j.1440-1797.2011.01548.x