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Intrinsic renal disease (nephrotic syndrome (secondary causes (Hep B/C…
Intrinsic renal disease
nephrotic syndrome
characterised by:
hypoalbuminaemia<25g/L
increased catabolism in proximal tubule
proteinuria >3.5g/day (ACR >250mg/mmol)
structural damage to glomerular barrier
oedema
increased salt and water retention
increased capillary hyrdaulic conductivity (TNFalpha and ANP)
primary causes
minimal change nephropathy
commonest cause in children
effacement of podocyte foot processes
70% of adults achieve remission with steroids but most relapse
idiopathic/NSAIDs/paraneoplastic
membranous nephropathy
20-30% in adults
idiopathic/malignancy/Hep B/drugs/autoimmunity
diffusely thickened GBM
spontaneous remission in 30%
antibodies against phospholipase A2 present in 80%
focal segmental glomerulosclerosis
may be idiopathic or secondary
HIV associated with collapsing subtype
50% have impaired renal function at diagnosis
spontaneous remission <10%
may respond to plasma exchange
mesangiocapillary glomerulonephritis
immune complex mediated
underlying cause in most cases
complement mediated
less common
extrarenal manifestations
prognosis poor
mesangial and endocapillary proliferation
thickened capillary basement membrane
double contouring of capillary walls
secondary causes
Hep B/C
usually membranous
Hep C can cause MCGN
SLE
membranous
diabetic nephropathy
amloidosis
pre-eclampsia
paraneoplastic
drug related