Glomerulonephritis Flashcards

1
Q

features of nephritic syndrome?

A

haematuria (can be microscopic or macroscopic)
oliguria
proteinuria (not as much as nephrotic so must be <3g)
fluid retention (can be central/peripheral/anywhere)

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2
Q

features of nephrotic syndrome?

A

peripheral oedema
proteinuria (3g or more in 24 hrs)
serum albumin <25g/L
hypercholesterolaemia

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3
Q

how are most types of glomerulonephritis treated?

A
immunosuppression (eg steroids)
BP control (ACE inhibitors or ARBs)
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4
Q

what does nephrotic syndrome predispose to?

A

thrombosis
hypertension
high cholesterol

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5
Q

most common cause of nephrotic syndrome in children?

A

minimal change disease

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6
Q

what usually causes minimal change disease?

A

idiopathic

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7
Q

how is minimal change disease usually treated?

A

steroids

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8
Q

most common cause of nephrotic syndrome in adults?

A

focal segmental glomerulosclerosis

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9
Q

what is IgA nephropathy also known as?

A

bergers disease

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10
Q

most common cause of primary glomerulonephritis (not caused by another disease)?

A

IgA nephropathy

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11
Q

peak age of presentation of IgA nephropathy?

A

20s

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12
Q

what does histology show in IgA nephropathy?

A

IgA deposits

glomerular mesangial proliferation

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13
Q

most common glomerulonephritis overall?

A

membranous glomerulonephritis

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14
Q

peak incidence of membranous?

A

bimodal peak

in 20s and 60s

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15
Q

what does histology show in membranous?

A

IgG and complement deposits on basement membrane

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16
Q

what causes membranous?

A

70% are idiopathic

can be secondary to malignancy, rheumatic disorders and drugs (eg NSAIDs)

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17
Q

how does post-strep glomerulonephritis present?

A

patients usually under 30
1-3 weeks after strep infection (tonsillitis or impetigo)
develop nephritic syndrome
usually a full recovery

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18
Q

what happens in goodpastures syndrome?

A

anti GBM antibodies attach glomerulus and pulmonary basement membranes
this causes glomerulonephritis and pulmonary haemorrhage

19
Q

classic picture of goodpastures disease?

A

acute kidney failure and haemoptysis

20
Q

what will histology show in rapidly progressive glomerulonephritis?

A

crescentic glomerulonephritis

21
Q

how does rapidly progressive glomerulonephritis usually present?

A

very acute illness with sick patients

often secondary to goodpastures

22
Q

what is glomerulonephritis?

A

group of kidney diseases mainly characterised by inflammatory disease primarily affecting the glomeruli
can be primary or secondary to other systemic disorder such as diabetes

23
Q

how can glomerulonephritis present?

A

nephrotic or nephritic

24
Q

types of primary glomerulonephritis?

A
membranous nephropathy
minimal change disease
focal segmental glomerulosclerosis
mesenagiocapillary (membranoproliferative)
IgA nephropathy
rapidly progressive glomerulonephritis
25
which types of primary glomerulonephritis present with nephrotic syndrome?
membranous nephropathy minimal change disease focal segmental glomerulosclerosis mesenagiocapillary (membranoproliferative)
26
which types of primary glomerulonephritis present with nephritic syndrome?
IgA nephropathy | rapidly progressive glomerulonephritis
27
types of rapidly progressive glomerulonephritis?
type 1 = anti-GBM disease type 2 = immune complex (SLE, HSP, IgA) type 3 = vasculitis
28
main cause of glomerulonephritis in kids?
minimal change disease
29
main cause of glomerulonephritis in adults in overall?
IgA nephropathy
30
how do most glomerulonephritis develop?
result of immune dysregulation which can be due to inappropriate response to self antigen or foreign antigen
31
diagnostic features of minimal change disease?
electron microscopy might show effacement of podocytes but light microscopy and immunofluorescence dont show any changes
32
second most common cause of glomerulonephritis in adults?
membranous
33
which type of glomerulonephritis can present nephrotic or nephritic?
mesangiocapillary (membranoproliferative)
34
what cause mesangiocapillary (membranoproliferative) glomerulonephritis?
immune deposition in the glomerulus, thickening of basement membrane and activation of complement pathway leads to glomerular damage
35
which type of glomerulonephritis is most associated with hep C?
mesangiocapillary (membranoproliferative)
36
diagnostic features of IgA nephropathy?
IgA deposition seen in glomerulus | presents with haematuria 1-2 days after symptoms of a URTI
37
how is glomerulonephritis diagnosed?
``` urinalysis routine bloods for renal function, clotting, LFTs, glucose and inflammatory markers immuno-serological screen imaging renal biopsy ```
38
how is urinalysis used in glomerulonephritis?
dipstick for urine anf blood culture and cytology microscopy can show dysmorphic red blood cells (low MCV) and casts
39
types of serology screening in glomerulonephritis?
``` ANCA anti-GBM ANA anti-dsDNA C3 and C4 HBV, HCV and HIV serum immunoglobulins and urine electrophoresis (exclude myeloma) ```
40
how is glomerulonephritis managed non pharmacologically?
lifestyle changes can help cases secondary to chronic disease (eg diabetes) salt and water restriction
41
how can glomerulonephritis be managed pharmacologically?
ACEi can decrease proteinuria and improve mortality steroids reduce immunological factors and induce remission diuretics help with oedema and BP control statins help lipids anticoagulation in nephrotic syndrome as it causes hypercoagulability cyclophosphamide can be used in resistant cases (immune related)
42
surgical management of glomerulonephritis?
renal transplant
43
types of secondary glomerulonephritis that present nephrotic?
diabetes SLE class 5-6 amylooid hepatitis B/C
44
what types of secondary glomerulonephritis present nephritic?
post-strep SLE class 1-4 vasculitis (HSP, GPA) goodpastures disease (anti-GBM)