Glomerulonephritis and systemic diseases Flashcards

1
Q

What are the 3 cardinal features of glomerular abnormalities?

A

1) Proteinuria
2) Haematuria
3) Urinary casts

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2
Q

What is membranous GN?

A

A thickened glomerular basement membrane as a result of subepithelial immune complex deposits of IgG and C3. Usually idiopathic but can be secondary to malignancy.

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3
Q

What is minimal change GN?

A

Podocyte foot processes fuse (seen on electron microscopy- immunological studies and light microscopy are normal)

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4
Q

What is the most common cause of incidental haematuria?

A

IgA nephropathy

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5
Q

What treatments are appropriate in all glomerulonephritis?

A

Aggressive blood pressure treatment
Statins
Avoid nephrotoxic drugs

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6
Q

What is the main treatment for minimal change GN?

A

Corticosteroids

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7
Q

How can we treat membranous GN with deteriorating renal function?

A

Regimens including steroids and cyclophosphamide, ciclosporin or rituximab.

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8
Q

How do we treat rapidly progressive GN?

A

More aggressive immunosuppressive regimens- including corticosteroids, cyclophosphamide and plasmapheresis.

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9
Q

How do we slow progression of renal disease in diabetes?

A

Aggressive blood pressure control:
ACE inhibitors and/or ARBs.

Good glycaemic control
Smoking cessation
Control of lipids
Antiplatelet agents (aspirin)

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10
Q

What are the pathologies causing renovascular disease?

A

1) Atherosclerotic renal artery stenosis.
2) Fibromuscular dysplasia.

Also: thromboembolism, renal artery dissection, cholesterol embolism

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11
Q

How does atherosclerotic renal artery stenosis present?

A

HTN
Renal impairment
If bilateral, pulmonary oedema

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12
Q

What are the 3 characterising features of HUS?

A

Haemolytic anaemia
Thrombocytopenia (platelet consumption)
acute renal failure

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13
Q

In which vasculitis do we find pANCA?

A

Microscopic polyangiitis

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14
Q

In which vasculitis do we usually find cANCA (in 90% of cases)?

A

Wegener’s granulomatosis (Granulomatosis with polyangiitis)

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15
Q

What does a renal biopsy show in Wegeners?

A

Focal necrotizing GN, sometimes with crescent formation and granuloma.

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16
Q

How do we treat Wegeners and microscopic polyangiitis?

A

Corticosteroids, cyclophosphamide (or rituximab) and plasmapheresis.

17
Q

What is Goodpasture’s syndrome characterised by?

A

Pulmonary haemorrhage (more common in smokers), haematuria, rapidly progressive renal failure.

Anti-GBM positive.

18
Q

Which systemic diseases can have renal involvement?

A
Diabetes mellitus
Myeloma
Amyloidosis
HUS
Renovascular disease
Renal vasculitis
Wegener's granulomatosis (granulomatosis with polyangiitis)
Microscopic polyangiitis
Goodpasture's syndrome
Polyarteritis nodosa (PAN)
SLE
Henoch-Schonlein purpura
Scleroderma
Cryoglobulinaemia