Glomerular Injury Flashcards
What is the difference between a primary and secondary glomerular injury?
Primary: just affecting the glomerulus
Secondary: a systemic disease that has, in turn, damaged the glomerulus
What are the 4 sites of glomerular injury?
- subepithelial: anything that affects podocytes side of glomerular BM
- Within glomerular basement
- Subendothelial: inside the BM
- Mesangial/paramesangial: supporting capillary loop
What is the pathology of proteinuria?
Protein in the urine is caused by podocyte damage and widening of the fenestration slits, causing protein to leak out
What defines nephrotic syndrome? What is the likely site of injury?
> 3.5g of protein filtered in 24 hours. Oncotic pressure reduces, giving rise to edema. Podocyte and subepithelial damage is likely
Name 3 primary causes of proteinuria/nephrotic syndrome
- Minimal change glomerulonephritis (GN)
- Focal segmental glomerulosclerosis (FSGS)
- Membranous glomerulonephritis
Define glomerulonephritis and 6 stimuli
Damage/inflammation of the glomerular BM resulting in altered function
- virus
- post-infective
- bacteria
- parasites
- drugs
- hereditary
How might a patient present with nephrotic/nephritic syndrome?
Nephrotic: low albumin, oedema, frothy urine
Nephritic: Increased BP, coca-cola urine, decreased urine output
Name 6 things you could do to investigate a patient who may have a glomerular disease
- Urine dip
- Urine microscopy
- BP
- Blood
- Biopsy
- Microscopy: light and electron
When does minimal change glomerulonephritis usually present? What is a good investigation to do?
Childhood - adolescence
Do a renal biopsy and electron microscopy to see podocyte damage
When does focal segmental glomerulosclerosis typically present?
What is the significance of the ‘sclerosis’
What might you see under electron microscopy?
Adulthood:
Podocytes undergo damage and scar (sclerosis)
May see a thickened BM
When/how does membranous glomerulonephritis typically occur?
What histological features might be noticed?
It is the most common cause of nephrotic syndrome in adults, and is caused by immune complex deposits in the sub-epithelial space (probably an autoimmune basis against podocytes)
Histology: ‘speckly BM’ and thickened capillary
What is IgA nephropathy?
How does it classically present?
The commonest glomerular nephropathy, occuring at any age and characterised by deposition of IgA antibody in the glomerulus. Classically presents with visible/invisible hematuria and normal C3 complement levels
Name the 2 hereditary nephropathies
Anti GBM BM and Alport syndrome
What are the 2 common secondary causes of proteinuria/nephrotic syndrome?
- Diabetes mellitus
2. Amyloidosis
What is goodpasture syndrome? What investigations could you do and what might you see?
Very rapidly progressing glomerular nephritis, caused by an autoantibody to collagen IV in BM (but only affects kidney)
Could do chest x-ray: see pulmonary infiltrates and microscopy to see depositions of IgG along the glomerular BM