» Articles » PMID: 490233

Microscopic Hematuria in School Children: Epidemiology and Clinicopathologic Evaluation

Overview
Journal J Pediatr
Specialty Pediatrics
Date 1979 Nov 1
PMID 490233
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

An unselected population of 8,954 children, age 8 to 15 years, was screened for hematuria. Four urine specimens from each were examined; microscopic hematuria was found in one or more specimens in 4.1%, and in two or more specimens in 1.1% of the children. The prevalence was not age or sex dependent. Those with two or more positive samples were re-examined twice during a half-year period: 33 had hematuria of 6 or more RBC/0.9 mm3, or more than 100,000 RBC/hour, on both occasions; renal biopsy performed on 28 of them revealed two cases of IgA-IgG nephropathy, one of focal segmental sclerosis, one of extracapillary glomerulonephritis, and one of possible hereditary nephritis. In 12 patients the biopsy was entirely normal; the rest showed equivocal changes. Co-existing proteinuria and the degree of hematuria correlated well with the severity of the morphologic alterations. Pathologic findings in microscopic hematuria seem to be less frequent than in hematuria in general; in most such patients, renal biopsy is probably not indicated. In some children the low-grade hematuria may merely represent the upper end of physiologic variation.

Citing Articles

Cracking the code: an integrated electronic medical record approach to early diagnosis of genetic kidney disease in children with microscopic haematuria.

Butler G, Satkumaran S, Shanks J, Segal A, Kausman J, Wilkins E Pediatr Nephrol. 2025; .

PMID: 39951044 DOI: 10.1007/s00467-025-06702-8.


Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria.

Liu J, Zhou D, Wang X, Shen T, Wang C, Dai R Ren Fail. 2024; 46(2):2423845.

PMID: 39540369 PMC: 11565656. DOI: 10.1080/0886022X.2024.2423845.


COL4A gene variants are common in children with hematuria and a family history of kidney disease.

Rheault M, McLaughlin H, Mitchell A, Blake L, Devarajan P, Warady B Pediatr Nephrol. 2023; 38(11):3625-3633.

PMID: 37204491 DOI: 10.1007/s00467-023-05993-z.


Clinical and diagnostic utility of genomic sequencing for children referred to a Kidney Genomics Clinic with microscopic haematuria.

Shanks J, Butler G, Cheng D, Jayasinghe K, Quinlan C Pediatr Nephrol. 2023; 38(8):2623-2630.

PMID: 36715773 DOI: 10.1007/s00467-022-05846-1.


Urinary Screening in Asymptomatic Indian Children: A Cross Sectional Epidemiological Study.

Banerjee M, Roy D, Lingeswaran M, Tomo S, Mittal A, Varma P EJIFCC. 2022; 33(3):242-251.

PMID: 36447804 PMC: 9644094.