Glomerulonephritis Flashcards

1
Q

Does focal segmental glomerulonephritis (FSGS) cause nephrotic or nephritic syndrome?

A

Nephrotic

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2
Q

What age does focal segmental glomerulosclerosis most commonly present?

A

Young adults (20-30)

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3
Q

What are the causes of focal segmental glomerulosclerosis?

A

Idiopathic
Secondary to other renal pathology e.g. IgA Nephropathy, reflux nephropathy
HIV
Heroin
Alport’s syndrome
Sickle-cell

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4
Q

What happens in renal transplants in patients with FSGS?

A

Commonly recurrs

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5
Q

What is seen on light microscopy in FSGS?

A

Focal and segmental sclerosis and hyalinosis on light microscopy

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6
Q

What is seen on electron microscopy in FSGS?

A

Effacement of foot processes

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7
Q

What is the management for FSGS?

A

Steroids and immunosuppressants

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8
Q

What is the commonest form of nephrotic syndrome in adults?

A

FSGS (unsure might be membranous)

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9
Q

How can you tell the difference between IgA nephropathy and post-streptococcal glomerulonephritis (AKA diffuse proliferative glomerulonephritis)?

A

IgA starts a day or two after URTI, whereas post-streptococcal is weeks after infection

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10
Q

What are the 4 main features of nephritic syndrome?

A

Haematuria (microscopic or macroscopic)
Oliguria
Proteinuria (less than 3g/day)
Fluid retention

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11
Q

What are the 4 main features of nephrotic syndrome?

A

Peripheral oedema
Proteinuria >3g/day
Serum albumin <25g/l
Hypercholesterolaemia (due to increased production and decreased metabolism)

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12
Q

What is the commonest form of glomerulonephritis in children?

A

Minimal change disease

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13
Q

What is the cause of minimal change disease?

A

Idiopathic

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14
Q

What is the management and prognosis of minimal change disease?

A

Steroids
Good prognosis

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15
Q

What syndromes do post-streptococcal and IgA nephropathy cause?

A

Nephritic

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16
Q

What is the commonest overall glomerulonephritis in adults?

A

Membranous glomerulonephritis

17
Q

Is membranous glomerulonephritis nephrotic or nephritic?

A

Nephrotic most common

18
Q

What is the peak incidence of membranous glomerulonephritis?

A

50-60 years

19
Q

What are the causes of membranous glomerulonephritis?

A

idiopathic
infections: hepatitis B, malaria, syphilis
malignancy: lung cancer, lymphoma, leukaemia
drugs: gold, penicillamine, NSAIDs
autoimmune diseases: systemic lupus erythematosus (class V disease), thyroiditis, rheumatoid

20
Q

What antibodies are involved in idiopathic membranous glomerulonephritis?

A

anti-phospholipase A2 antibodies

21
Q

What does membranous glomerulonephritis look like on electron microscopy?

A

the basement membrane is thickened with subepithelial electron dense deposits. This creates a ‘spike and dome’ appearance

22
Q

What is the management of membranous glomerulonephritis?

A

ACEI or ARB (reduced proteinuria and improves prognosis)
Combination of steroid and cyclophosphamide in severe or progressive disease (many patients spontaneously improve)
Anticoagulation for high risk patients

23
Q

What is the prognosis for membranous glomerulonephritis?

A

Prognosis - rule of thirds
one-third: spontaneous remission
one-third: remain proteinuric
one-third: develop ESRF