Glomerulonephritis Flashcards

1
Q

what are 5 examples of glomerular disease

A

diabetic nephropathy, pyelonephritis (infection), glomerulonephritis (inflamm), amyloid nephropathy, transplant nephropathy

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2
Q

what is glomerulonephritis

A

inflammation of the glomeruli usually by an autoimmune response

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3
Q

what are types of glomerulonephtis (4)

A

nephritic syndrome (proteinuria), nephritic syndrome (haematuria), mixed, rapidly progressive

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4
Q

what antibody mediated responses can cause glomerulonephritis (4)

A

intrinsic antigen, deposition of immune complexes, T cell mediated

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5
Q

what can cause circulating immune complexes

A

infection eg hep C, HIV // drugs eg gold // cancer eg lymphoma

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6
Q

what types of vasculitis can cause glomerulonephritis

A

GPA and MPA

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7
Q

what secondary causes can cause glomerulonephritis

A

infection, drugs, malignancies, systemic eg ANCA vasculitis GPA and MPA, LUPUS

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8
Q

what are symptoms of glomerulonephritis

A

haematuria (nephritic syndrome), proteinuria (nephrotic syndrome), HYPERTENSION, AKI, CDK, ESRD

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9
Q

how do you diagnose glomerulonephritis

A

BP, bloods, urinalysis, kidney biopsy

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10
Q

what investigations are done on the kidney biopsy

A

light microscopy, electro-microscopy, immunofluorescence

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11
Q

what is seen in light microscopy

A

hypercellularity, inflamm cells, sclerosis and crescents (bad)

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12
Q

what is seen in electron microscopy

A

basement membrane deposits

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13
Q

what is seen in immunoflueroscence

A

antibody type

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14
Q

what is proliferative glomerulonephritis

A

proliferation of mesengial cells

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15
Q

what is focal vs diffuse disease

A

focal <50% of glomeruli affected and diffuse >50%

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16
Q

what are crescents associated with

A

bad prognosis

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17
Q

what are the treatment aims of glomerulonephritis

A

reduce proteinuria, induce remission, preserve long-term renal function

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18
Q

what non-immunosuppresive treatment can be used in glomerulonephritis

A

anti-hypertensives, ACEi/ ARBs, diuretics, statins

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19
Q

what immunosuppressive drugs are used to treat glomerulonephritis (6)

A

steroids eg prednisolone, azathioprine, cyclophosphate, caclineurin inhibitors, IV immunoglobulin, plasmapheresis

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20
Q

what cells are the site of injury in nephrotic syndrome and what does this result in

A

podocytes: protein in urine and atrophies and loss of charge barriers

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21
Q

is nephrotic syndrome proliferative or non-proliferative

A

non-proliferative

22
Q

what are the signs of nephrotic syndrome (5)

A

proteinuria >3g/day, hypoalbuminaemia, oedema, hypercholestraemia, normal renal function

23
Q

what is the main protein lost in nephrotic syndrome

24
Q

what are complications of nephrotic syndrome

A

infection, renal vein thrombosis, PE, volume depletion

25
what are the 3 main categories of nephrotic syndrome
minimal change, focal segmental glomerulosclerosis, membranous
26
what is the most common cause of nephrotic syndrome in children
minimal change
27
what is the most common cause of nephrotic syndrome in adults
FSGS
28
what is the 2nd most common cause of nephrotic syndrome in adults
membranous
29
what types of nephrotic syndrome are likely to cause progressive renal failure
FSGS: 50% get ESRF in 10 years // membranous: 40% get ESRF with slow progression
30
what type of renal biopsy do you do in minimal change nephrotic syndrome and what does it show
light microscopy - looks normal and is associated with good prognosis
31
how do you treat minimal change nephrotic syndrome
oral steroids (94% remission) 2nd line cyclophosphamide
32
what type of renal biopsy do you do in FSGS nephrotic syndrome and what does it show
immunoflueroscence: minimal Ig // light: rosneal appearance
33
how do you treat FSGS
60% remission with steroids. 2nd line ciclosporin
34
what does a renal biopsy show membranous nephrotic syndrome
sub-epithelial immune complex in basement
35
how do you treat membranous nephrotic syndrome
steroids/ alkylating agents eg cyclophosphamide + all on ACEi's
36
what cells are the site of injury in nephritic syndrome and what does this result in
mesangial cells: release chemokines --> inflamm /// endothelial --> vasculitis
37
is nephritic syndrome proliferative or non-proliferative
proliferative - due to mesangial cell involvement
38
how does nephritic syndrome present (6)
hypertension + haematuria, acute renal failure oliguria, oedema, henoch schonlein purpura (HSP)
39
what is the most common cause of GN in the world
IgA nephropathy (nephritic)
40
what are the symptoms if IgA nephropathy
asymptomatic haematuria, macroscopic haematuria after resp/ GI infection, HSP
41
what is seen on a renal biopsy for IgA nephropathy
IgA deposits in mesangium and mesangial hypercellularity
42
how commonly does IgA nephropathy progress to ESRF
25%
43
how do you treat IgA nephropathy
BP control, ACE/ARBs, fish oil
44
what is membranoproliferative GN
mixed nephrotic and nephritic syndrome
45
what is seen in a biopsy of membranoproliferative GN
hypercellular glomeruli + thick membranes
46
what is rapidly progressive GN
rapid deterioration of acute renal failure that is treatable
47
what is rapidly progressive GN associated with
active urinary sediment, glomerular crescent on biopsy
48
what are ANCA+ive causes of rapidly progressive GN
GPA, MPA
49
what are ANCA-ive causes of rapidly progressive GN
goodpastures, HSP, SLE
50
how do you treat rapidly progressive GN
steroids + cyclophsophamide/ azathioprine + supportive dialysis