Glomerulonephritis Flashcards

1
Q

What are the clinical features in nephritic syndrome?

A

Haematuria (visible or non-visible)
Oliguria (reduced output)
Proteinuria < 3g/24hr
Fluid retention

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2
Q

What are the criteria for nephrotic syndrome?

A

All of:

  • peripheral oedema
  • proteinuria >3g/24hr
  • serum albumin <25g/l
  • hypercholesterolaemia
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3
Q

What is the difference between glomerulonephritis and interstitial nephritis?

A

Glomerulonephritis - inflammation of/around the glomerulus

Interstitial nephritis - inflammation of the space between cells and tubules (interstitium)

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4
Q

What is glomerulosclerosis and what causes it?

A

Scarring of the glomerulus caused by:

  • any glomerulonephritis
  • obstructive uropathy
  • focal segmental glomerulosclerosis
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5
Q

How are most types of glomerulonephritis treated?

A

Immunosuppression e.g. steroids

Blood pressure control with ACEi or ARBs

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6
Q

What are the different types of glomerulonephritis?

A
Minimal change disease
Focal segmental glomerulosclerosis
Membranous GN
IgA nephropathy (mesangioproliferative GN or Berger's disease)
Post streptococcal GN (diffuse proliferative GN)
Mesangiocapilliary GN
Rapidly progressive GN
Goodpastures syndrome
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7
Q

How do patients with nephrotic syndrome usually present?

A
Oedema 
Frothy urine (proteinuria)
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8
Q

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

A

Minimal change disease

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9
Q

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

A

Focal segmental glomerulosclerosis

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10
Q

What are the features of minimal change disease?

A

Nephrotic syndrome in children
Idiopathic
Responds well to steroids

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11
Q

What is IgA nephropathy also called?

A

Berger’s disease

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12
Q

What is the peak age for IgA nephropathy? What are the features?

A

20s

1-2 days post URTI

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13
Q

What is seen on histology in IgA nephropathy?

A

IgA deposits + glomerular mesangial proliferation

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14
Q

What is the most common type of glomerulonephritis? What age of patients typically get it?

A

Membranous GN

- peak in 20s and 60s

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15
Q

What causes membranous GN?

A
Majority idiopathic
May be secondary to:
- malignancy
- rheumatoid disorders
- drugs e.g. NSAIDs
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16
Q

What is seen on histology in membranous GN?

A

IgG and complement deposits on the basement membrane

17
Q

What are the features of post streptococcal GN?

A

Patients under 30:

  • 1-3 weeks post strep infection (tonsillitis or impetigo)
  • nephritic syndrome
  • usually full recovery
18
Q

What are the features of goodpasture syndrome?

A

Anti-GBM antibodies attack glomerulus and pulmonary basement membranes
–> glomerulonephritis (AKI) + haemoptysis

19
Q

What are the features of rapidly progressive GN?

A

Very acute illness with sick patient but responds well to treatment

20
Q

What does histology show in rapidly progressive GN?

A

Crescentic glomerulonephritis