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Updated: Jul 21, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Acute glomerulonephritis in children. An evolutive morphologic and immunologic study of the glomerular inflammation
Insights
This study tracked children with acute nephritic syndrome, finding that most cases involved streptococcal infections. Follow-up biopsies revealed varying recovery rates, with a significant portion showing persistent or worsening kidney lesions.
Area of Science:
- Pediatric Nephrology
- Immunology
- Infectious Diseases
Background:
- Acute nephritic syndrome is characterized by proteinuria, hematuria, edema, and hypertension in children.
- Streptococcal infections are a common trigger for acute nephritic syndrome in pediatric populations.
- Renal biopsy is crucial for diagnosing and understanding the progression of glomerulonephritis.
Purpose of the Study:
- To investigate the clinical and morphologic evolution of acute nephritic syndrome in children.
- To correlate clinical presentation with renal biopsy findings over time.
- To assess the long-term renal outcomes following streptococcal infection-associated nephritic syndrome.
Main Methods:
- Prospective study of 80 children diagnosed with acute nephritic syndrome.
- Initial renal biopsies within 60 days of disease onset, with follow-up biopsies in 46 patients between 6 and 45 months.
- Analysis included light microscopy, immunofluorescence, and electron microscopy, alongside clinical data.
- Detection of streptococcal infection in 73 out of 80 cases.
Main Results:
- 77 patients exhibited C3 deposits in renal biopsies, indicating active glomerulonephritis.
- Follow-up biopsies showed complete resolution in 27% of cases.
- 56% of patients had residual minor lesions, while 17% showed increased severity of kidney damage.
- 3 patients with typical clinical symptoms lacked morphologic evidence of glomerulonephritis.
Conclusions:
- Acute nephritic syndrome, often linked to streptococcal infections, shows diverse recovery patterns in children.
- A significant proportion of children experience persistent or progressive renal lesions despite initial treatment.
- Renal biopsy is essential for monitoring disease activity and predicting long-term prognosis in pediatric nephritic syndrome.
Abstract:
This study deals with 80 children showing a clinically typical acute nephritic syndrome with proteinuria and/or hematuria, edema, and hypertension. Their ages ranged between 2 years 5 months and 16 years; 36 cases were female. In 73 cases a streptococcal infection was demonstrated; the remaining 7 cases did not show morphologic differences with the former. No previous renal disease nor familial history of nephropathies were elicited. In every case a renal biopsy was obtained in the first 60 days of clinical disease; in 46 cases a second renal biopsy was obtained sometime between 6 and 45 months since the beginning of the disease. In 3 cases the renal tissue was considered to be normal by light microscopy, immunofluorescence and electron microscopy in both the first and second biopsies. These 3 patients were not considered as cases of morphologic acute glomerulonephritis in spite of showing a typical clinical picture and they are not included in the evaluation of the glomerular inflammatory evolution. In all the remaining 77 cases C3 granular and segmentary intramembranous and mesangial dense deposits were found in the first biopsy. The second biopsy showed morphologic and immunologic normalization in 27% of the cases, slight lesions in 56% and an increase in severity in 17% of the cases.
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