Post-streptococcal glomerulonephritis (PSGN) is an acute nephritic syndrome caused by an immunological response to group A streptococcal (GAS) infection.
It is the most common cause of acute nephritis in children. The incidence peaks between 6 and 15 years of age. Boys are affected twice as much as girls.
- Causes
- Sporadic GAS infection
- Epidemic GAS infection
- Pathophysiology
- Throat or skin nfection with group A streptococcus
- Production of antibodies against the streptococcal antigens:
- Nephritis-associated plasmin-like receptor (NAPIr)
- Streptococcal pyrogenic exotoxin B (SPE B)
- In situ immune complex formaiton in the glomerular membrane
- Activation of complement and inflammation
- Damage to the glomerulus
- Subendothelial deposits cause haematuria and reduced glomerular filtration rate
- Subepithelial (’hump’) deposits cause proteinuria
- Signs and symptoms
- Pharyngitis or skin infection
- The incidence of PSGN is higher following skin infection that pharyngitis
- Clinical features appear 1 – 3 weeks after pharyngitis, and 3 – 6 weeks after skin infection
- It amay be asymptomatic
- Generalised oedema
- Respiratory distress due to pulmonary oedema
- Hypertension
- Microscopic haematuria
- Gross haematuria
- Tea or cola-coloured urine
- Oliguria
- Pharyngitis or skin infection
- Differentials
- IgA nephropathy
- C3 glomerulopathy
- Post-infectious glomerulonephritis
- Glomerulonephritis due to:
- Viral hepatitis
- Infective endocarditis
- Lupus nephritis
- IgA vasculitis (Henoch Schonlein Purpura)
- Investigations
- Urinalysis to confirm haematuria and quantify proteinuria
- Dysmophic RBCs with or without casts
- Mild proteinuria (nephrotic range proteinuria may also be present)
- Urean and creatinine
- A normal creatinine does not exclude severe renal dysfunction
- Throat or skin swab for culture to confirm the presence of GAS
- Serology (streptozyme test)
- Anti-streptolysin O (ASO)
- Anti-hyaluronidase (AHase)
- Anti-streptokinase (ASKase0
- Anti-DNAse B
- Anti-nicotinamide-adenine dinucleotidase (anti-NAD)
- Low C3 levels
- Renal biopsy is the definitive diagnostic test
- Diffuse glomerular cellular infiltration and endocapillary proliferation on light microscopy
- Diffuse granular deposits of C3 and IgG on immunofluorescence
- Subepithelial (dome-shaped ‘humps’) and subendothelial deposits on electron microscopy
- Urinalysis to confirm haematuria and quantify proteinuria
- Treatment
- Treat fluid overload
- Salt and water restriction
- Diuretics
- Monitor blood pressure and treat hypertension
- ACE-inhibitors should be used with caution due to the risk of hyperkalaemia
- Dialysis if indicated
- Antibiotics if there is persistent streptococcal infection
- Treat fluid overload
- Complications
- Pulmonary oedema
- Hypertensive encephalopathy
- Acute kidney injury
- Renal failure