Glomerulonephritis Flashcards
What are the clinical presentations of glomerulonephritis? (5)
- Isolated haematuria and/or proteinuria
- Nephrotic syndrome
- Nephritic syndrome
- RPGN
- CKD
Isolated Haematuria
Microscopic vs gross haematuria
RBC 3 or more RBC/hpf or 10x10^6 cells/L
Exclude urological causes
Glomerular haematuria - RBC cast, dysmorphic RBCs
Causes: IgAN, thin membrane disease, Alport’s disease
Isolated Proteinuria
Non-nephrotic range vs nephrotic range
- Proteinuria > 0.3g/day to 3.5g/day
- Nephrotic range haematuria >3.5g/day
Non-glomerular causes: overflow or tubular proteinuria
Non-persistent: functional proteinuria, orthostatic
Persistent proteinuria: glomerular causes
Nephrotic Syndrome
Proteinuria > 3.5g/day
Hypoalbuminaemia < 25 - urine loss of albumin , inadequate compensatory hepatic synthesis
Oedema - change in Starling forces, reduced oncotic pressure, sodium retention (tubular defect)
Hyperlipidaemia - increased hepatic synthesis, defective lipoprotein lipase activity, increased urine loss of HDL
Mechanism:
Increased glomerular permeability and loss of protein in urine
Complications of Nephrotic syndrome
- Hypercoagulability
- AKI - volume depletion, ATN, interstitial oedema, drugs, renal vein thrombosis
Causes of Nephrotic Syndrome
- Common (5)
- Less common (3)
Common
1. Minimal change disease
2. FSGS
3. Membranous nephropthy
4. Diabetic nephropathy
5. Amyloidosis
Less common
6. MPGN type 1
7. Dense drposit disease
8. Cryoglobulinaemic MPGN
Nephritic Syndrome
Reduced GFR and oliguria
Haematuria with RBC cast
Variable degree of proteinuria (non-nephrotic range)
Oedema
Hypertension (due to urinary retention)
Mechanism
Inflammatory injury of glomerular capillary wall
Causes of Nephritic Syndrome
Common
1. IgAN
2. Lupus
3. Infection
Less common
4. ANCA
5. MPGN
RPGN
Rapid loss of renal function (days to weeks) with oliguria or anuria
Features of glomerulonephritis, dysmorphic erythrocyturia, RBC casts, glomerular proteinuria
Crescenteric GN
Pathological term - extracapillary proliferation due to focal rupture of glomerular capillary wall
Presence of crescents in > 50% of glomeruli
Causes of RPGN / CGN
- Anti-GBM disease - Goodpasture’s syndrome if pulmonary haemorrhage
- Pauci-immune GN - systemic vasculitis or renal limited disease
- Immune complex GN
How to differentiate between other causes of rapid renal failure vs RPGN/CGN ?
Differentials - rapid loss of renal function and oliguria but NO dysmorphic RBCs, RBC casts, substatial proteinuria
- Acute thrombotic microangiopathy
- Atheroembolic renal disease
- ATN
- Acute tubulointerstitial nephritis
CKD
Chronic glomerulonephritis with slowly progressive renal impairment
No clinical event early in the course of disease to bring to medical attention
Late presentation: hypertension, proteinuria, renal impairment
Biopsy not appropriate (shrunken kidneys)
Initial Investigations for GN
- Blood - FBC, RP, LFT with albumin
- UFEME
- Urine ACR/PCR
- 24 hour total urine protein
- US kidneys +/- RAS Doppler
- +/- CT KUB or contrasted CT AP
Further Investigations for Nephrotic Syndrome
- Myeloma panel (paraproteinaemia, amyoidosis, MM)
- Serum anti-PLA2R (idiopathic membranous GN)
- Anti-thrombospondin (malignancy immune-mediated membranous GN) (send to Mayo)
- C3, C4 (post-infectious, SLE, C3/C4 GN)
- ANA, dsDNA (SLE panel)
- Virology: Hep B, Hep C, HIV (membranous, cryoglobulinaemia, side effect of medication, screen pre-treatment)
Further Investigations for Nephritic Syndrome
- C3, C4
- Anti-dsDNA
- Virology
- ANA
- ANCA: anti-MPO, anti-proteinase 3
- Cryoglobulin
- Anti-GBM