Glomerular Disease Flashcards

1
Q

A young man develops macroscopic haematuria 1-2 days after URTI?

A

IgA nephropathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Definition of Glomerulonephritis?

A

Immune mediated disease of the kidneys affecting the glomeruli. There is disruption somewhere in the 3 layered barrier of the glomerulus leading to haematuria/ and or proteinuria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Damage to endothelial or mesangial cells results in a ___1_____ and ___2______
Damage to the podocytes leads to a ____3______ and _____4_____

A

1) proliferative lesion
2) haematuria
3) non-proliferative lesion
4) proteinuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How can glomerulonephritis be classified?

A

By clinical syndrome
By histological classification
By cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the 5 clinical syndromes glomerulonephritis can cause?

A

1) Asymptomatic proteinuria or haematuria
2) Acute glomerulonephritis/ acute nephritic syndrome
3) Chronic glomerulonephritis
4) Rapidly progressive glomerulonephritis
5) Nephrotic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

GLOMERULONEPHRITIS CLINICAL SYNDROME

Asymptomatic proteinuria or haematuria?

A

Just have the proteinuria or haematuria and this signals mild glomerular damage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

GLOMERULONEPHRITIS CLINICAL SYNDROME

Acute glomerulonephritis/ Nephritic Syndrome?

A

Haematuria, acute fall in GFR, Na+ and H2O retention and hypertension. Oedema but less so than nephrotic.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

GLOMERULONEPHRITIS CLINICAL SYNDROME

Chronic Glomerulonephritis?

A

Slow progressive damage, proteinuria, haematuria, hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

GLOMERULONEPHRITIS CLINICAL SYNDROME

Rapidly progressive glomerulonephritis?

A

Very rapid renal failure, oliguria, haematuria, proteinuria, usually without other symptoms of nephritic syndrome (ie hypertension and oedema)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

GLOMERULONEPHRITIS CLINICAL SYNDROME

Nephrotic syndrome?

A

Consists of heavy proteinuria leading to hypoalbuminaemia and oedema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

4 histological classifications of glomerulonephritis explain?

A

1) Proliferative or Non-proliferative
- presence or absence of proliferation of mesangial cells
2) Focal or diffuse
- < or > 50% glomeruli affected
3) Global or segmental
> all or part of glomerulus affected
4) Crescenteric
> presence of crescents which are epithelial cell extra capillary proliferations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

3 types of non-proliferative glomerulonephritis?

A

1) Minimal change glomerulonephritis
2) Focal segmental glomerulosclerosis
3) Membranous glomerulonephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

4 types of proliferative glomerulonephritis?

A

1) IgA nephropathy
2) Post infectious Glomerulonephritis
3) Membranoproliferative glomerulonephritis
4) Rapidly progressive glomerulonephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Minimal change glomerulonephritis presents as ______

A

nephrotic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Minimal change glomerulonephritis accounts for ____ of all nephrotic syndrome in kids and ______

A

80% in children

20% in adults

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Does minimal change glomerulonephritis cause progressive renal failure?

A

No

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Describe histology of minimal change glomerulonephritis?

A

No abnormalities on light microscopy but electron microscopy reveals abnormal fused podocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

No abnormalities on light microscopy but electron microscopy reveals abnormal fused podocytes

A

Minimal change glomerulonephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Focal segmental glomerulosclerosis presents as ____

A

nephrotic syndrome

20
Q

Non proliferative glomerulonephritis usually present as ____

A

nephrotic syndrome

21
Q

Focal segmental glomerulosclerosis is associated with ____

A

HIV, obesity, kidney reflux disease, heroin use and gene mutations

22
Q

_____ of focal segmental glomerulosclerosis progress to renal failure

23
Q

Treatment of focal segmental glomerulosclerosis?

A

Prolonged steroids can help but 50% still progress to renal failure

24
Q

Membranous glomerulonephritis presents as _____

It is ____ progressive

A

nephrotic syndrome

slowly

25
Membranous glomerulonephritis causes?
usually idiopathic but can be associated with heptatits B/ parasites, SLE, malignancies, penicillamine
26
Describe microscopy of membranous glomerulonephritis?
Immune complex deposition and complement activation against the glomerular basement membrane proteins results in microscopically thickened glomerular basement membrane. Immunofluorescene shows IgG uptake
27
_____ of membranous glomerulonephritis progresses to end stage renal disease
30%
28
Treatment of membranous glomerulonephritis?
Steroids, alkylating agents, B cell monoclonal antibodies
29
What is the most common glomerulonephritis?
IgA nephropathy (a sort of non-systemic form of HSP)
30
IgA nephropathy presents as ______
nephritic syndrome
31
IgA nephropathy often occurs ____
24-48hrs after an URTI
32
IgA nephropathy on biopsy?
Mesangial cell proliferation and expansion of light microscopy with IgA deposits in mesangium on IF.
33
Management of IgA nephropathy?
No specific management, lower BP with ACEi/ ARB potentially steroids, many people have recurrence even after transplant
34
When does post infectious glomerulonephritis usually occur?
Typically occurs 2 weeks after an infection usually strep pyogenes
35
Treatment of post infectitious glomerulonephritis?
Only need supportive treatment usually recovers
36
Membranoproliferative glomerulonephritis presents with _____
combined nephritic and nephrotic syndrome
37
What happens in membranoproliferative glomerulonephritis? Histology?
Subendothelial deposition of immune complexes | Thickened basement membrane and mesangium
38
Causes of membranoproliferative glomerulonephritis?
SLE or hepatitis
39
Treatment and prognosis of membranoproliferative glomerulonephritis?
Has poor prognosis need to treat underlying cause
40
What conditions present as rapidly progressive glomerulonephritis?
All can present but Vasculitis ANCA +ve GPA, EGPA and MPA Goodpastures only present as rapidly progressing other common are SLE and HSP
41
Rapidly progressive glomerulonephritis results in _____
rapid progression to renal failure over weeks
42
Immune complexes can be a cause of glomerulonephritis but where can we get circulating immune complexes from?
Auto-immune diseases e.g. SLE Infection- hepatitis, bacteria, HIV Drugs- gold penicillamine Cancer often lymphomas
43
Complications of nephrotic syndrome?
Pulmonary emboli Infection (loss of immunoglobulins) Renal vein thrombosis (loss of clotting factors) Hypovolaemia
44
Treatment of nephrotic syndrome?
Fluid + salt restriction Diuretic ACE inhibitor IV albumin if hypovolaemia
45
Minimal change nephropathy can occur after _____ or ______
infection or allergic reaction