Glomerulonephritis/ Polycystic kidneys Flashcards

1
Q

What is the normal excretion level of protein in the urine?

A

< 150mg

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2
Q

What is the gold standard test for measuring protein levels in the urine?

A

24hr urine collection

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3
Q

What is the standard practice for the assessment of protein levels in the urine?

A
  1. ACR - Urine albumin creatine ratio

2. PCR - Urine protein creatine ratio

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4
Q

Name 5 potential syndromes that abnormalities occurring in the glomerulus may present with

A
  1. Isolated haematuria/ proteinuria or haematoproteinuria
  2. Nephrotic syndrome
  3. Acute glomerulonephritis (acute nephritic syndrome)
  4. Rapidly progressive glomerulonephritis
  5. Chronic kidney disease including ESRD
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5
Q

What is the most common cause of nephrotic syndrome in children?

A

Minimal change disease

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6
Q

Suggest 2 medications which may cause nephrotic syndrome

A
  1. NSAIDS

2. Penicillamine

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7
Q

What are Kimmelstiel-Wilson lesions?

A

Mesangial nodules seen on renal biopsy that are associated with diabetic nephropathy

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8
Q

Outline the classical presentation of a patient with IgA nephropathy

A

Haematuria occurring 1-3 days after an upper respiratory tract infection

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9
Q

Give 2 examples of large vessel vasculitis

A
  1. Takayasu

2. Giant cell arteritis

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10
Q

Give 2 examples of medium vessel vasculitis

A
  1. Polyarteritis nodosa

2. Kawasaki disease

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11
Q

Recall the 4 types of ANCA associated vasculitis

A
  1. Granulomatosis with polyangitis (Wegener’s)
  2. Microscopic polyangitis
  3. Eosinophilic granulomatous polyangitis (Churg-Strauss syndrome)
  4. Renal limited vasculitis
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12
Q

Uric acid crystals on urine microscopy is most commonly seen in what condition?

A

Tumour lysis syndrome

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13
Q

Why do we consider anti-coagulation in heavily proteinuric patients?

A

Heavy proteinuria causes loss of antithrombin III, proteins C and S through the tubules

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14
Q

Outline the 5 management components of a patient with nephrotic syndrome

A
  1. Salt restriction - Advised no salt diet
  2. Fluid restriction to 1-1 1/2 L per 24hrs
  3. Diuretics
  4. Add ACEi/ARB
  5. Role of anticoagulation
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15
Q

Name 4 autosomal dominant causes of renal cystic disease

A
  1. ADPKD
  2. Tuberous sclerosis
  3. Von Hippel Lindau Disease
  4. Medullary cystic disease
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16
Q

Give 2 autosomal recessive causes of renal cystic disease

A
  1. ADPKD

2. Juvenile onset Nephronphthisis

17
Q

Name 2 X linked causes of renal cystic disease

A
  1. Orofacial digital syndrome

2. Chromosomal disorders (Trisomy 13/18/21)

18
Q

Name 3 developmental causes of renal cystic disease

A
  1. Medullary sponge kidney
  2. Multicystic dysplastic kidney
  3. Pyelocalyceal cysts
19
Q

Name 3 causes of acquired cysts

A
  1. Simple cysts
  2. Acquired renal cystic disease
  3. Hypokalaemia related cysts
20
Q

Name 3 precautions required for patients that are taking Tolvaptan

A
  1. Patient needs regular blood tests including renal and liver function
  2. Patient needs to drink plenty of fluid
  3. Annual MRI volume measurement of the kidneys is required