Glomerulonephritis Flashcards

(35 cards)

1
Q

What is glomerulonephritis?

A

kidney disease that result from immunologic and inflammatory injury to the glomeruli

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2
Q

What are the features of nephrotic syndrome?

A

proteinuria, hypoalbuminaemia, oedema, hyperlipidaemia, variable haematuria, normo or hypertensive, variable GFR decline

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3
Q

What are the features of nephritic syndrome?

A

haematuria, hypertension, rapidly progressive GFR, may have nephrotic range proteinuria

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4
Q

What are the pathogenic types of GN?

A

immune complex GN, pauci-immune GN, anti GBM GN, monoclonal Ig GN, C3 glomerulopathy

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5
Q

What is immune complex GN?

A

characterised by granular deposits of polyclonal Ig

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6
Q

What are the main types of immune complex GN?

A

IgA nephropathy, lupus nephritis, fibrillary GN, infection related GN

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7
Q

What is the most common cause of primary GN?

A

IgA nephropathy

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8
Q

Which patients typically get IgA nephropathy?

A

males in teens to 20s

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9
Q

How do most patients with IgA nephropathy present?

A

with macroscopic haematuria

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10
Q

What are other less common ways that IgA nephropathy can present?

A

flank pain, fever, microscopic haematuria, mild proteinuria, malignant HTN, AKI

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11
Q

What other diseases is IgA nephropathy associated with?

A

cirrhosis, coeliac disease, HIV, minimal change disease, membranous GN, GPA

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12
Q

What are the indications for renal biopsy in IgA nephropathy?

A

persistent protein excretion, elevated serum creatinine, new onset hypertension, significant elevation in BP above previous stable baseline

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13
Q

When does lupus nephritis usually develop?

A

within 3-36 months of diagnosis of SLE

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14
Q

What regular testing should be done for patients with SLE?

A

urinalysis, spot PCR, serum creatinine, eGFR, dsDNA, complement levels

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15
Q

Which SLE patients should get a renal biopsy?

A

most patients who develop evidence of renal involvement (not if protein <0.5g/day)

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16
Q

What are the characteristic histopathological findings on renal biopsy for lupus nephritis?

A

glomerular deposits that stain predominantly for IgG but have co-deposits of IgA, IgM, C3 and C1q

17
Q

How do you diagnosis infection related GN?

A

kidney biopsy, preceding or concurrent infection, low C3

18
Q

What is the differential diagnosis for infection related GN?

A

SLE, cryoglulinaemia, C3 glomerulopathy, IgA, ANCA

19
Q

What are the risk factors for infection related GN?

A

male, diabetes, immunocompromised, alcoholism, malignancy, malnutrition, synthetic heart valve, IVDU, AIDS, TB

20
Q

What is pauci immune GN?

A

characterised by negative or few Ig deposits on IF (can be either ANCA positive or negative)

21
Q

Which ANCA do patients with GPA usually have?

22
Q

Which ANCA do patients with MPA usually have?

23
Q

Which has higher relapse rates GPA or MPA?

24
Q

Which histological subtype of pauci immune GN has the best survival?

25
Which histological subtype of pauci immune GN has the worst survival?
sclerotic
26
What is anti GBM GN?
characterised by linear deposits of Ig and frequently C3 along the GBM
27
What blood test confirms anti GBM GN?
anti GBM antibodies
28
What is the histological pattern of anti GBM GN?
severe necrotising and crescentic pattern
29
What are the associations with anti GBM GN?
smoking, hydrocarbons, alemtuzumab, HLA DR2
30
How do patients with anti GBM GN usually present?
with rapidly progressive GN and often with alveolar haemorrhage
31
What is the treatment for anti GBM GN?
plasma exchange, steroids, cytotoxic therapy
32
What is monoclonal Ig GN?
Monotypic Ig deposits in the kidney often associated with underlying monoclonal gammopathy
33
What are cryoglobulins?
circulating immunoglobulins that reversibly precipitate on cooling of the serum and redissolve on rewarming
34
What are the 3 types of cryoglobulins?
type 1 - single monoclonal immunoglobulin, due to underlying haematologic malignancy type 2 - mixed cryoglobulin, associated with underlying viral infections, dysproteinaemias or autoimmune diseases type 3 - mixed cryoglobulin associated with autoimmune diseases or infections
35
What causes C3 glomerulopathy?
dysregulation and persistent activation of the alternative complement pathway