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Acute Post-Streptococcal Glomerulonephritis in Children: A Comprehensive Review
Sérgio Veloso Brant Pinheiro1, Victor Buchini de Freitas2, Gustavo Valverde de Castro2
1Department of Pediatrics, Unit of Pediatric Nephrology, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
Insights
Acute post-streptococcal glomerulonephritis (APSGN) is a kidney injury in children caused by Streptococcus infections. While often resolving spontaneously, understanding its pathogenesis and preventing complications is key to reducing morbidity.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Immunology
Background:
- Acute post-streptococcal glomerulonephritis (APSGN) is an immune-complex mediated glomerular disease.
- It is triggered by Group A Streptococcus (GAS) infections and is a significant cause of acquired kidney injury in children.
Purpose of the Study:
- To review recent evidence on APSGN, covering epidemiology, pathogenesis, clinical and laboratory findings, histopathology, treatment, and prognosis.
- To provide an overview of this common childhood kidney disease.
Main Methods:
- Non-systematic review of current literature on APSGN.
- Discussion of epidemiological data, pathogenic mechanisms, clinical presentation, diagnostic findings, and therapeutic approaches.
Main Results:
- APSGN incidence is higher in developing countries (24.3/100,000) than developed countries (6.2/100,000).
- Key streptococcal antigens (e.g., nephritis-associated plasmin receptor, streptococcal pyrogenic exotoxin B) activate the complement system, leading to IC deposition and glomerulonephritis.
- Classic presentation includes nephritic syndrome (hematuria, oliguria, hypertension, edema) with characteristic histopathological findings of diffuse proliferative glomerulonephritis.
Conclusions:
- The pathogenesis of APSGN requires further elucidation.
- No specific treatment exists, but management focuses on preventing and treating complications, leading to generally good prognosis with rare progression to chronic kidney disease.
Background:
Acute post-streptococcal glomerulonephritis (APSGN) is an immune- complex (ICs) mediated glomerular disease triggered by group A β-hemolytic streptococcus (GAS) or Streptococcus pyogenes infections. APSGN represents a major cause of acquired kidney injury in children.
Methods:
This non-systematic review summarizes recent evidence on APSGN. We discuss the epidemiology, pathogenesis, clinical and laboratory findings, histopathology, treatment and prognosis of the disease.
Results:
The median APSGN incidence in children in developing countries is estimated at 24.3/100,000 per year, compared with 6.2/100,000 per year in developed countries. Nephritis-associated plasmin receptor, identified as glyceraldehyde-3-phosphate dehydrogenase, and the cationic cysteine proteinase streptococcal pyrogenic exotoxin B are thought to be two leading streptococcal antigens involved in the pathogenesis of APSGN, which activate the complement system, mainly via the alternative but also the lectin pathway. This process is critical for the generation of inflammation by the ICs deposited in the glomerulus. The classic phenotype is an acute diffuse proliferative glomerulonephritis leading to features of the nephritic syndrome, including hematuria, oliguria, hypertension and edema. The histopathology shows that the glomeruli are diffusely affected, mostly presenting enlarged glomerular tuffs due to hypercellularity. Proliferative endothelial and mesangial cells and inflammation have also been observed. APSGN frequently has spontaneous recovery. There is no specific therapy, but its morbidity and mortality are drastically reduced by the prevention and/or treatment of complications.
Conclusion:
Despite recent advances, the pathogenesis of APSGN is not fully understood. There is no specific treatment for APSGN. The prognosis is generally good. However, some cases may evolve into chronic kidney disease.
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