Renal plz last one Flashcards

1
Q

In young people what will cause renal artery stenosis?

And what is the treatment?

A

Fibromuscular dysplasia

Balloon Angioplasty

*ACE inhibitors are contraindicated in renal artery stenosis as they maintain kidney perfusion

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2
Q

What metabolic changes occur with dialysis?

A

Amyloidosis

Dyslipidaemia

Secondary hyperparathyroidism

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3
Q

List three causes of bilateral enlarged kidneys:

A

Bilateral Hydronephrosis

Renal cell carcinomas or tumours (tubal sclerosus)

Polycystic kidney disease

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4
Q

Which disease is minimal change disease corrloaed with?

A

Hodgkin’s lymphoma

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5
Q

When should protein: creatinine ratio be done?

A

Early morning

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6
Q

What general investigations can be conducted into nephritic syndrome?

A

Nephritic is characterised by blood in the urine and thus has a wide range of causes. General investigations include:

Bloods:

  • FBC (anaemia)
  • U&Es
  • LFTs (hypoalbuminemia)
  • Anti-Streptolysin O antibodies
  • Complement levels
  • Autoimmune markers

Orifices:
- PCR (early morning)

X-rays:
- US of kidneys (identify parenchymal abnormalities)

Special tests:
- Percutaneous biopsy

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7
Q

What are some symptoms of minimal change disease?

A

Discomfort related to swelling:

  • puffy eyes
  • skin break down

Abdominal discomfort

Tiredness

Foamy urine

Increased infections

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8
Q

What are some differentials to nephrotic syndrome?

A

Malnourishment (low albumin)

Liver disease (poor albumin)

Excess protein loss through burns or injuries

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9
Q

What is general management of nephrotic syndrome?

A

Steroids
Dietary sodium restriction and Fluid management
Prophylactic antibiotics
Vaccinations

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10
Q

In RA list two causes that could lead to nephrotic syndrome:

A

Amyloidosis

NSAID use

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11
Q

How is poly arteritis nodosa diagnosed?

A

Renal Angiography

Renal biopsy

*can also look for Hep B serology

Treated:

  • Azathioprine
  • steroids
  • HTN control
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12
Q

What are the three types of renal tubular acidosis syndromes and what do you expect to see?

A

Type II: Defect in PCT

  • reduced HCO3- absorption
  • Fanconni syndrome
  • Heavy mental poisnoning
  • Acetazolaimide (blocks carbonic anhydrase)

Type I:

  • Distal tube
  • build up of H+ and K+
  • Lithium
  • Sjorgens syndrome

Type IV:

  • Aldosteronism defect
  • build up of H+ and K+
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