Nephrotic Syndromes Flashcards

(28 cards)

1
Q

What are the characteristics of nephrotic syndrome?

A
  • Oedema
  • Proteinuria (>3.5g/day)
  • Hypoalbuminemia
  • Hypogammaglobulinemia
  • Hypercoagulable state
  • Hyperlipidemia and hypercholsterolemia
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2
Q

What will the urine look like on nephrotic syndrome?

A

Frothy

- Will have fatty casts

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3
Q

Why is nephrotic syndrome associated with a hypercoagulable state?

A

Antithrombin III is lost in the urine

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4
Q

What coagulation factors does ATIII affect?

A

2, 9, 10, 11

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5
Q

Why is nephrotic syndrome associated with an increased risk of infection?

A

Loss of IgGs in urine (hypogammaglobinemia)

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6
Q

What is the most common nephrotic syndrome in children?

A

Minimal change disease

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7
Q

What can primary minimal change disease be caused by?

A
  • Idiopathic
  • Immunisation
  • Immune stimulus
  • Infection

4 i s

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8
Q

What can secondary minimal change disease be due to?

A

Lymphoma (cytokine-mediated change)

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9
Q

What is minimal change disease treated with?

A

Corticosteroids

- Primary disease has excellent response

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10
Q

What is minimal change disease also known as?

A

Lipoid nephrosis

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11
Q

What histology show in minimal change disease?

A

Light Microscopy - Normal glomeruli (lipid may be seen in PCT cells)

Negative immunoflouresence

Electron Microscopy - Effacement of podocyte foot processes

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12
Q

What groups of people have a higher risk of Focal Segmental Glomerulosclerosis?

A

Black people

Secondary disease may be due to:

  • HIV
  • Sickle cell
  • Heroin
  • Obesity
  • Interferon treatment
  • Congenital malformations
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13
Q

What can FSGS be treated with?

A

Steroids - inconistent response

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14
Q

What will light microscopy show in FSGS?

A

Segmental sclerosis and hyalinosis

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15
Q

What will Immunoflouresence show in FSGS?

A
  • Often negative

- May be positive for nonspecific focal deposits of IgM, C3, C1

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16
Q

What will electron microscopy show in FSGS?

A

Effacement of foot processes similar to minimal change disease

17
Q

What is membarnous nephropathy also known as?

A

Membranous glomerulonephritis

18
Q

What is membranous nephropathy’s response to corticosteroids like?

A

Poor response

19
Q

What is primary membranous nephropathy due to?

A

Antibodies to phospholipase A2 receptor (anti-PLA2R)

20
Q

What is secondary membranous nephropathy due to?

A
  • Infection: HCV, HBV
  • Autoimmune: SLE
  • Medications (NSAIDs, Penicillamine, Gold)

IMA Proud member of the spike and dome club

21
Q

What will light microscopy show in membranous nephropathy?

A

Diffuse capillary and GBM thickening

22
Q

What will immunoflouresence show in membranous nephropathy?

A

Granular due to immune complex (IC) deposition

23
Q

What will electron microscopy show in membranous nephropathy?

A

“Spike and Dome” appearence of epithelial deposits

24
Q

What chronic conditions can predispose to amyolid deposition?

A
  • AL amyloid
  • AA amyloid
  • Prolonged dialysis
25
What will light microscopy show in Amyloidosis?
Congo red stain will show apple green birefringence under polarised light due to amyolid deposition in mesangium
26
What is the mst common cause of end stage renal failure in the USA?
Diabetic glomerulonephropathy
27
Describe the pathophysiology of diabetic glomerulo-nephropathy?
Hyperglycemia - > Nonenzymatic glycation of tissue proteins - > Mesangial expansion; GBM thickening and increased permeability - > Hyperfiltration (glomerular HTN and increased GFR) - > Glomerular hypertrophy and glomerular scarring (glomerulosclerosis) - > Further progression of nephropathy
28
What will light microscopy show in diabetic glomerulonephropathy?
- Mesangial expansion - GBM thickening - Eosinophilic nodular glomerulosclerosis (Kimmelstiel-Wilson lesions)