Glomerulonephritis (GN) Flashcards

(47 cards)

1
Q

define GN

A

immune-mediated disease of the kidneys affecting the glomerular capillary wall

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2
Q

how do endothelial cells respond to injury?

A

vasculitis

haematuria

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3
Q

how do podocytes respond to injury?

A

atrophies increase gap size of the barrier

proteinuria

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4
Q

how does the mesangium respond to injury?

A

proliferation and chemokines

haematuria

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5
Q

presentation of GN

A

haematuria
proteinuria
nephrotic/nephritic syndrome
hypertension

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6
Q

classification of proteinuria

A

Microalbuminuria (30-300mg albuminuria/day)
Asymptomatic proteinuria (<1g/day)
Heavy proteinuria (1-3g/day)
Nephrotic syndrome (>3g/day)

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7
Q

diagnosis of GN

A

urinarlysis (haematuria, proteinuria, granular casts, RBCs, lipiduria)
bloods
kidney biopsy (LM, IF, EM)

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8
Q

non-immunosuppressant management options of GN

A
anti-hypertension (<130/80, <120/75 if proteinuria)
ACEI/ARB
diuretics
statins
anticoagulants
antiplatelets
fish oil
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9
Q

immunosuppressant management options for GN

A
corticosteroids 
azathioprine
alkylating agents (cyclophosphamide)
calcineurin inhibitors (cyclosporin)
plasmapheresis (TPE)
antibodies
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10
Q

what are granular casts?

A

precipitation of Tamm-Horsfall mucoprotein in low pH

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11
Q

types of casts

A

hyaline (benign)
red cells (pathological)
leucocytes (infection/inflammation)
granular (chronic disease)

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12
Q

what does the presence of RBC casts in urine prove?

A

haematuria is glomerular

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13
Q

two classes of GN

A

primary

secondary

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14
Q

examples of secondary causes of GN

A

infection
drugs
systemic-ANCA, SLE, GP, HSP

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15
Q

what are the five types of idiopathic/ primary GN?

A
  1. minimal change
  2. focal segmental glomerulosclerosis (FSGS)
  3. membranous nephropathy
  4. IgA nephropathy
  5. membranoproliferative
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16
Q

who does minimal change present in?

A

children

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17
Q

presentation of minimal change GN

A

facial/ generalised oedema

nephrotic proteinuria

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18
Q

diagnosis of minimal change GN

A

normal renal biopsy with slight gaps between podocytes

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19
Q

management of minimal change GN

A

complete remission with steroids

20
Q

causes of FSGS

A

obesity
HIV
sickle cell
IV drug users

21
Q

what is the commonest cause of nephrotic syndrome in adults?

22
Q

diagnosis of FSGS

A

renal biopsy LM shows minimal Ig/complement deposition with podocyte fusion/sclerosis

23
Q

management of FSGS

A

some have remission on steroids

can progress to ESRF

24
Q

two types of membranous nephropathy

A
  1. primary

2. secondary

25
secondary causes of membranous nephropathy
``` HepB parasites SLE carcinoma of lung, colon melanoma lymphoma syphilis NSAIDs captopril gold penicillamine ```
26
diagnosis of membranous nephropathy
immune complex deposition (anti-PLA2r Ab and C3) in BM with thickened membrane on silver stain (spiky)
27
management of membranous nephropathy
steroids alkylating agents B cell monoclonal Ab
28
what can membranous nephropathy progress to?
ESRF
29
which is the commonest type of GN?
IgA nephropathy
30
presentation of IgA nephropathy
``` non-nephrotic proteinuria haematuria following resp/GI infection AKI/CKD Coeliac's HSP ```
31
diagnosis fo IgA nephropathy
biopsy shows mesangial cell proliferation | LM IgA deposits in mesangium
32
management of IgA nephropathy
BP control ACEI/ARB fish oil
33
what can IgA nephropathy progress to?
ESRF
34
causes of membranoproliferative GN
hep C SLE malignancy
35
who gets membranoproliferative GN?
adults and children
36
presentation of membranoproliferative GN
nephritic | nephrotic
37
diagnosis of membranoproliferative GN
thick membranes- tram tracks
38
what is rapidly progressive GN (RPGN)?
rapid deterioration of renal function over days/weeks
39
diagnosis of RPGN
active urinary sediment (RBCs, granular casts) | glomerular crescents on biopsy
40
causes of RPGN
any GN | ANCA +ve and -ve
41
management of RPGN
immunosuppression plasmapheresis dialysis if needed
42
presentation of nephritic syndrome
``` renal failure (high K+) oliguria haematuria oedema hypertension ```
43
diagnosis of nephritic syndrome
active urinary sediment (RBCs, granular casts)
44
nephrotic syndrome presentation
proteinuria can have normal renal function facial swelling oedema
45
diagnosis of nephrotic syndrome
proteinuria >3g/day hypoalbuminuria (<30) low complement hypercholesterolaemia
46
complications of nephrotic syndrome
``` infections renal vein thrombosis PE volume depletion (diuretics) vitamin D deficiency hypothyroidism ```
47
management of nephrotic syndrome
``` fluid and salt restriction diuretics ACEI/ARB anticoagulants immunosuppression ```