Glomerulonephritis Flashcards

1
Q

define nephrotic syndrom

A

Albumin <30 g/L
Proteinuria >3g/24 hours
+/- oedema

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2
Q

5 presentations of GN

A
Asymptomatic urinary abnormalities
CKD
Nephrotic syndrome
Nephritic syndrome
Rapidly progressive GN
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3
Q

2 roles of mesangial cells

A

structure

communication

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4
Q

what is the specialisation of the epithelial cell of the capillary loop?

A

fenestration

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5
Q

what type of cell is a podocyte

A

epithelial

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6
Q

role of podocytes

A

important in charge and size permeability of the barrier

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7
Q

4 responses of podocytes to injury

A

apoptosis

foot process effacement

detachment from GBM

loss of slit diaphragm

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8
Q

3 examples of glomerular diseases

A

minimal change disease
FSGS- Focal segmental glomerulosclerosis
diabetic nephropathy

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9
Q

4 primary causes of nephrotic disease

A

focal segmental glomerulosclerosis

membranous

minimal change

membranoproliferative

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10
Q

5 secondary causes of nephrotic disease

A

drugs e.g. NSAIDs, tamoxifen, lithium, antimicrobials

infections e.g. HIV, hep B, hep C, syphilis, malaria

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11
Q

3 types of investigations into nephrotic disease

A

immunology e.g. ANA, dsDNA, C3 and C4, myeloma screen

microbiology e.g. hep B and C

radiolog e.g. renal USS +/- doppler, CXR

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12
Q

5 complications of nephrotic disease

A

thromboembolism- loss of anticoag factors

infection- loss of IgG

hyperlipidaemia- loss of LDLR

nutrition

AKI- renal vein problems

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13
Q

what do you see on microscopy in minimal change

A

normal light microscopy

diffuse foot effacement on electron microscopy

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14
Q

5 secondary causes of minimal change

A
H and NHL
malignant thymoma
renal cell carcinoma
GVHD
lithium
NSAIDs
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15
Q

3 categories of causes that can cause focal segmental glomerulosclerosis

A

familial e.g. mutation in nephrin gene

virus associated e.g. HIV, EBV

medication e.g. ecstasy

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16
Q

primary cause of membranous nephropathy

A

autoimmune reaction of a circulating antibody directed to a specific antigen on the podocyte surface

17
Q

3 mechanisms of glomerular immune complex deposition

A
  • circulating immune complex trapping
  • in situ immune deposit formation (exogenous antigens)- ag and ab from within the body meet in the kidney
  • in situ immune deposit formation (endogenous antigens)- abs meet ags already in the kidney
18
Q

What is the most common cause of glomerulonephritis

A

IgA nephropathy

19
Q

basic pathophysiology of IgA nephropathy

A

mesangial cell deposition of IgA

20
Q

how do we classify vasculitis

A

according to size of blood vessel involved