Glomerulonephritis Flashcards

(38 cards)

1
Q

common causes of glomerular disease (4)

A

diabetic nephropathy, glomerulonephritis, amyloid nephropathy, transplant glomerulonephropathy

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2
Q

commonest cause of renal failure in adults

A

diabetic nephropathy

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3
Q

second commonest cause of renal failure in adults

A

chronic glomerulonephritis

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4
Q

Pathogenesis behind glomerulonephritis

A

immune mediated disease of the kidneys affecting the glomeruli with tubulointerstitial damage - usually driven by antibodies

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5
Q

3 different patterns of injury in glomerulonephritis

A

Mesangial cells, endothelial cells, podocytes

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6
Q

Proliferative injury in glomerulonephritis (2)

A

endothelial or mesangial cells

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7
Q

how do mesangial cells cause proliferative damage in the kidney?

A

release Ang II, vasoconstric, cause chemokines and inflammatory cells

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8
Q

How do endothelial cells cause proliferative damage in the kidneys?

A

cause a vasculitis which causes rapid damage to the kidney

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9
Q

How does damage to podocytes cause kidney damage?

A

podocytes atrophy causing loss of the barrier and thus protein but no blood will leak

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10
Q

Nephrotic syndrome is a triad of…

A

hypoalbuminaemia, proteinuria, oedema

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11
Q

Presentation of nephrotic syndrome may be…

A

mild increase in BP, normal to mild decrease in GFR

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12
Q

Nephritic syndrome tends to have…

A

proteinuria, haematuria (micro/frank) and potentially hypoalbuminaemia

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13
Q

Presentation of nephritic syndrome may be…

A

mod-severe increased in BP, mod-severe decrease in GFR

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14
Q

How does glomerulonephritis lead to increased BP?

A

damage to glomerulus restricts blood flow, leading to compensatory BP increase to try and restore flow

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15
Q

How does glomerulonephrities lead to protein and blood in the urine?

A

damage to podocytes leads to protein and blood leaking into urine

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16
Q

Glomerulonephritis likely to cause nephrotic syndrome

A

Membranous, minimal change, FSGS, mesangiocapillary

17
Q

Secondary causes of nephrotic syndrome

A

diabetes, SLE, amyloid, Hep B/C

18
Q

Glomerulonephritis likely to cause nephritic syndrome

A

IgA nephropathy, Mesangiocapillary

19
Q

Secondary causes of neprhitic syndrome

A

Post-streptococcal, vasculitis, Anti-GBM

20
Q

Blood tests to do to assess glomerulonephritis

A

FBC, U&Es, LFTs, ESR, CRP, Ig, Complement, autoantibodies

21
Q

What autoantibodies should be tested for in glomerulonephritis?

A

ANCA, Anti-GBM, dsDNA, ANA, HBsAg

22
Q

What tests (general) should be done to assess glomerulonephritis?

A

Blood tests, urine, imaging, ?Renal biopsy

23
Q

What imaging should be done to assess glomerulonephritis?

A

CXR

Renal USS

24
Q

Why are ACEi and ARBs useful in management of glomerulonephritis?

A

decreased proteinuria, decrease BP

25
Commonest glomerulonephritis in developed world
IgA nephropathy
26
How does IgA nephropathy normally present?
haematuria (micro/frank)
27
Typical patient for IgA nephropathy
young man with episodic haematuria but well between attacks
28
Features of Henoch Schonlein Purpura
purpuric rash on extensor surfaces, flitting polyarthritis, abdo pain, nephritis
29
What is Henoch Schonlein Purpura?
A systemic variant of IgA nephropathy causing a small vessel vasculitis
30
Anti-GBM autoantibodies are specifically against?
Type IV collagen
31
Where is Type IV collagen found?
in the basement membranes of the lung and kidney - causes pulmonary haemorrhage in smokers
32
Treatment of Anti-GBM glomerulonephritis
plasma exchange + steroids +/- cytotoxics
33
What is post-streptococcal glomerulonephritis?
diffuse, proliferative GN occuring 1-12 weeks after a sore throat of skin infection
34
Tests for post-streptococcal glomerulonephritis?
Anti-streptolysin O and decreased C3
35
Biopsy findings in rapidly progressive GN
all have crescents affecting the glomeruli
36
3 categories of rapidly progressive GN
immune complex disease (45%), ANCA +ve disease (50%), anti-GBM (5%)
37
How does rapidly progressive GN present?
AKI +/- systemic features - pulmonary haemorrhage is the commonest cause of death in ANCA +ve patients
38
Treatment for rapidly progressive GN
immunosuppression, steroids, plasma exchange and cyclophosphamide