Paget's Flashcards

1
Q

Cause of Paget’s disease

A
  • increased but uncontrolled bone turnover
  • excessive osteoclastic resorption followed by increased osteoblastic activity.
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2
Q

Which bones are most commonly affected with paget’s disease

A

skull
spine
pelvis
long bones of the lower extremities

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3
Q

Predisposing factors

A

increasing age
male sex
northern latitude
family history

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4
Q

What percentage of patients with Paget’s are symptomatic?

A

5%

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5
Q

Stereotypical patient

A
  • older male
  • bone pain
  • isolated raised ALP
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6
Q

If symptomatic, what are the main clinical features?

A

bone pain (e.g. pelvis, lumbar spine, femur)

classical, untreated features: bowing of tibia, bossing of skull

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7
Q

Typical blood test results

A

raised ALP
calcium/phosphate = normal Hypercalcaemia with prolonged immobilisation

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8
Q

Markers of bone turnover

A
  • procollagen type I N-terminal propeptide (PINP)
  • serum C-telopeptide (CTx)
  • urinary N-telopeptide (NTx)
  • urinary hydroxyproline
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9
Q

XR findings in Paget’s

A

osteolysis (early)
mixed lytic/sclerotic lesions (late)

skull = thickened vault, osteoporosis circumscripta

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10
Q

Indications for treatment in Pagets disease

A
  • bone pain
  • skull or long bone deformity
  • fracture
  • periarticular Paget’s
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11
Q

Management of Paget’s

A

bisphosphonate
calcitonin is less commonly used now

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12
Q

Complications of Paget’s Disease

A

deafness (cranial nerve entrapment)
bone sarcoma
fractures
skull thickening
high-output cardiac failure

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13
Q
A
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