Glomerulonephritis Disease Flashcards

1
Q

define IgA neuropathy

A

a type of glomerulonephritis characterised by IgA deposits within the glomeruli mesangium

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2
Q

cause of IgA neuropathy

A

increased synthesis of IgA that forms immune complexes easily trapped within the mesangium, causing build up and responses that trigger damage

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3
Q

clinical features of IgA neuropathy

A

gross or microscopic haematuria
hypertension
facial + leg oedema
recent respiratory illness

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4
Q

investigations of IgA neuropathy

A

bloods (FBC, U+Es, RFTs, creatinine)
urinalysis + MC&S
renal biopsy with immunofluorescence staining

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5
Q

common findings on investigations in IgA neuropathy

A

urine: +ve RBC + protein + WBCs
biopsy: IgA +C3 deposits in granular pattern in basement membrane

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6
Q

conservative management of IgA neuropathy

A

monitor and optimise fluid balance

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7
Q

medical management of IgA neuropathy

A

ACE inhibitors and ARBs

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8
Q

indications for use of corticosteroids (e.g. prednisolone) in IgA neuropathy

A

severe inflammatory damage

rapidly declining kidney function

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9
Q

define post-streptococcal glomerulonephritis (post strep GN)

A

a type of glomerulonephritis commonly occurring 1-2wks following a strep throat infection

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10
Q

clinical features of post-strep GN

A

acute insidious onset of haematuria, oliguria, hypertension and periorbital oedema
previous streptococcal illness 1-6wks ago

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11
Q

investigations of post-strep GN

A

urinalysis MC&S
bloods (FBC, U+Es, and immunoglobulins)
renal biopsy

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12
Q

common findings on investigations of post-strep GN

A

biopsy: IgG and C3 subepithelial deposition
urine: +ve blood + protein

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13
Q

management of post-strep GN

A

supportive measures

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14
Q

define anti-glomerular basement membrane disease (Goodpastures)

A

a genetic autoimmune condition characterised by a combo of glomerulonephritis, alveolar haemorrhage and circulating anti-GBM antibodies

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15
Q

risk factors of goodpastures disease

A
genetics (HLA-DRB1)
smoking 
exposure to organic solvents/hydrocarbons 
infection 
cocaine inhalation 
occupational exposure to metal dusts
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16
Q

clinical features of goodpastures disease

A
fluctuating fever 
nausea + vomiting 
weight loss 
chest pain + SOB 
oedema 
haematuria 
arthralgia
17
Q

investigations of Goodpastures disease

A

bloods (FBC, U+Es, ESR, antinuclear antibodies and complement)
CXR
renal or lung biopsy

18
Q

management of Goodpastures disease

A

plasmapheresis

high dose oral prednisolone or cyclophosphamide

19
Q

requirements of renal transplant in Goodpastures disease

A

end stage renal disease
serum anti-GBM antibodies undetectable for 12 mnths
disease remission for 6mnths

20
Q

define minimal change disease

A

a disease of the kidneys occurring due to minimal histological changes in the nephrons

21
Q

clinical features of minimal change disease

A

facial swelling that spreads to oedema
nausea + vomiting
abdominal pain
lethargy

22
Q

investigations of minimal change disease

A

urine dipstick

bloods (FBC, U+Es, LFTs)

23
Q

management of minimal change disease

A

fluid restriction and ⬇️ salt intake
corticosteroids (prednisolone)
human albumin and furosemide

24
Q

investigation findings in minimal change

A

+ve protein

25
define membranous glomerulonephritis
the most common type of glomerulonephritis in adults
26
causes of membranous glomerulonephritis
anti-phospholipase A2 antibodies hepatitis B malignancy
27
clinical features of membranous glomerulonephritis
oedema of face and legs recurrent infections fatigue SOB
28
investigation findings of membranous glomerulonephritis
basement membrane thickening with subepithelial electron dense deposits "spike and dome" appearance
29
investigations of membranous glomerulonephritis
bloods (FBC, LFTs, RFTs, lipid and coagulation screen) urine dipstick US KUB CXR + AXR
30
management of membranous glomerulonephritis
ACE inhibitor or ARB | immunosuppression (corticosteroid + cyclophosphamide)