Glomerulonephritis Flashcards

(38 cards)

1
Q

What is the definition of nephrotic syndrome?

A

Proteinuria >3.5g/24 hours
Hypoalbuminaemia <30g/L
Peripheral oedema

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2
Q

What is the definition of nephritis syndrome?

A

Haematuria
Hypertension
Oliguria

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3
Q

What are the potential causes of nephrotic syndrome?

A
Minimal change disease
Focal segmental glomerulonephropathy
Membranous glomerulonephropathy
Thin basement membrane disease
Fibronectin glomerulonephropathy
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4
Q

What are the potential causes of nephritic disease?

A
IgA nephropathy
Goodpastures syndrome
Membranoproliferative glomerulonephropathy
Post-infectious glomerulonephropathy
Granulomatosis with polyangiitis
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5
Q

What are the specific complications associated with nephrotic syndrome?

A

Thromboembolism

Risk of infection

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6
Q

What are the potential complications of glomerulonephropathy?

A
Risk of infection
Hypervolaemia
Hypertension
Hypercholesterikaemia
Hypercoagulability
CV disease
AKI
CKD
End stage renal disease
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7
Q

What is Rapidly progressive glomerulonephritis?

A

Acute nephritic syndrome alongside formation of crescents (due to the thrombosis and rupture of glomerular capillaries compressing surrounding glomerular structures)

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8
Q

What age group of patients is most likely to have rapidly progressing glomerulonephritis?

A

20 - 50 years

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9
Q

What investigations should be conducted for glomerulonephritis?

A

Bloods - U&Es, glucose, ANA, anti-dsDNA, ANCA, complement, Hep B/C, HIV, paraprotein, anti-GBM antibodies, anti-steptolysin O antibody,

Urinalysis - protein, blood
Urine protein creatinine ratio
Urine microscopy
Renal ultrasound

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10
Q

What management strategies form part of the basic treatment of glomerulonephritis?

A

ACEi/ARB
VTE prophylaxis
Fluid / salt restriction or sometimes diuretics
Treatment of the underlying cause

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11
Q

What is the most common cause of nephrotic syndrome in children?

A

Minimal change disease

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12
Q

What findings will be seen on immunofluorescence, light microscopy and electron microscopy in minimal change disease?

A

Immunofluoresence and light microscopy - unremarkable

Electron microscopy - fusion of podocyte foot processes

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13
Q

How is minimal change disease managed?

A

Nutritional support
Salt and fluid restriction
Corticosteroids
If steroids fail, rituximab

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14
Q

What findings will be seen on immunofluorescence, light microscopy and electron microscopy in focal segmental glomerulosclerosis?

A

Immunofluoresence and light microscopy - unremarkable

Electron microscopy - segmental scarring of certain glomeruli and fusion of podocyte fusion processes

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15
Q

What is the management official segmental glomerulosclerosis?

A

Generally supportive

Steroids in some patients

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16
Q

What are the potential causes of focal segmental glomerulosclerosis?

A

Primary - genetic mutations

Secondary - HIV, lupus, reflux nephropathy

17
Q

What is the most common cause of nephrotic syndrome in adults?

A

Focal segmental glomerulosclerosis

18
Q

What age group of patients are most commonly affected by membranous glomerulonephritis?

A

Age 30-50 years

19
Q

What are the potential causes of membranous glomerulonephritis?

A

Idiopathic
Hep B
Malaria
Lupus

20
Q

What findings will be seen on immunofluorescence, light microscopy and electron microscopy in membranous glomerulonephritis?

A

Microscopy - thickening glomerular basement membrane

Immunofluorescence - diffuse uptake of IgG

21
Q

How is membranous glomerulonephritis managed?

A

Steroids for progressive disease

Supportive care

22
Q

What is the most common type of nephritic syndrome in adults?

A

IgA nephropathy

23
Q

How long after an upper respiratory tract infection does IgA nephropathy usually present?

24
Q

What findings will be seen on immunofluorescence, light microscopy and electron microscopy in IgA nephropathy?

A

Microscopy - increase numbers of mesangial cells

Immunohistochemistry - IgA deposition within mesangial cells

25
What is the management of IgA nephroapthy?
Supportive care Steroids Immunosuppressants in some cases
26
How long after upper respiratory tract infection does post-strep glomerulonephritis usually present?
2 weeks later
27
What investigations findings are typically seen in post-strep glomerulonephritis?
Diffuse proliferative and exudative glomerular histology Dominant C3 staining and subepithelial humps Raised serum strep titres
28
What is the management of post-strep glomerulonephritis?
Mostly supportive (it is usually self-limiting)
29
What conditions are associated with membranoproliferazive glomerulonephritis?
Hep C | Autoimmune disease e.g. SLE
30
What investigations findings are typically seen in membranoproliferative glomerulonephritis?
Thickening basement membrane and mesangium Tram tracking appearance Subendothelial deposition of IgG
31
How is membranoproliferative glomerulonephritis managed?
Steroids in children | Antiplatelets in adults
32
What respiratory complications can occur in Goodpasture's syndrome?
Pulmonary haemorrhage
33
What investigations findings are typically seen in goodpastures syndrome?
Serum anti-GBM antibodies | IgG deposits along basement membrane on immunohistochemistry
34
How is good pastures syndrome managed?
High dose immunosuppression - steroids and cyclophosphamide +/- plasmapheresis
35
What investigations findings are typically seen in granulomatosis with polyangiitis?
Positive c-ANCA | Leukocytoclastic vasculitis with necrosis and granulomatous inflammation
36
How is granulomatosis with polyangiitis managed?
Immunosupression induction with high dose steroids and Rituximab / cyclophosphamide Maintenance therapy - steroids, methotrexate
37
What investigations findings are typically seen in microscopic polyangiitis?
Positive p-ANCA antibodies | Anaemia
38
How is microscopic polyangiitis managed?
Long term steroids / cyclophosphamide