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Published on: November 1, 2018
[Outcome of rapidly progressive glomerulonephritis post-streptococcal disease in children]
Manel Jellouli1, Sondos Maghraoui1, Kamel Abidi1
1Service de pédiatrie, hôpital Charles-Nicolle, 2037 Tunis, Tunisie.
Insights
Severe post-streptococcal glomerulonephritis in children can lead to kidney failure. Supportive dialysis was the key factor for renal survival in this study of rapidly progressive glomerulonephritis.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Glomerular Diseases
Background:
- Rapidly progressive glomerulonephritis (RPGN) is a rare, severe form of postinfectious glomerulonephritis.
- Post-streptococcal glomerulonephritis (PSGN) is a common cause of acute nephritis in children.
- This study focuses on severe PSGN presenting as RPGN.
Purpose of the Study:
- To describe the clinical outcomes of children with severe post-streptococcal glomerulonephritis.
- To identify factors influencing renal survival in pediatric RPGN secondary to streptococcal infection.
Main Methods:
- A retrospective study of pediatric patients diagnosed with severe PSGN between 1997 and 2009.
- Analysis of clinical presentation, renal biopsy findings, treatment modalities, and long-term renal function.
- Included 27 children with a mean age of 8.7 years, all presenting with renal failure.
Main Results:
- All 27 children presented with renal failure; 6 had nephrotic syndrome.
- Renal biopsies revealed crescents in 24 cases, indicating severe glomerular damage.
- While 66.6% received corticosteroids and 22% received corticosteroids with cyclophosphamide, only supportive dialysis (required by 11 patients) significantly improved renal survival (P=0.015).
- At follow-up, 81.5% achieved normal kidney function, but 3 progressed to end-stage renal disease.
Conclusions:
- Severe post-streptococcal glomerulonephritis, presenting as RPGN, is uncommon but carries a significant risk of poor renal outcomes.
- Despite advancements in supportive care, outcomes remain challenging.
- Supportive dialysis emerged as a critical factor for preserving kidney function in this cohort.
Background:
Rapidly progressive glomerulonephritis is a rare form of postinfectious glomerulonephritis. The aim of this study was to describe the outcome of our patients with severe post-streptococcal glomerulonephritis.
Methods:
This retrospective study was conducted in the department of pediatrics in Charles-Nicolle Hospital during a period of 13 years (1997-2009).
Results:
Twenty-seven children were identified. The mean age was 8.7 years. All patients presented renal failure at presentation. The mean serum creatinine at presentation was 376.9 μmol/L. Six patients presented nephrotic syndrome. Twenty-six children had renal biopsies. Renal biopsies showed crescents in 24 cases. Eighteen children received pulse dose of corticosteroids (66.6%) and 6 children (22%) received pulse dose of corticosteroids and cyclophosphamide. Eleven patients required dialysis. At last follow-up, 22 patients (81.5%) had normal kidney function, 2 had renal dysfunction and 3 reached end stage renal disease. The only significant determinant for renal survival was the supportive dialysis (P=0.015).
Conclusion:
Rapidly progressive glomerulonephritis is uncommon. There have been significant advancements in supportive, as well as specific therapy, but the outcome continues to be poor.
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