Discuss the basic epidemiology, pathophysiology, presentation, investigation, management and prognosis of bony metastasis Flashcards

1
Q

What are sunray spicules?

A

calcification within the tumour but outside the bone

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2
Q

How are secondary bone tumours formed?

A
  1. neovascularisation of 1º tumour cells leads to the cancer invading the blood vessels
  2. this causes tumour cell embolism as the cancer cells circulate the circulatory system
  3. tumour cells activate osteoclasts to reabsorb the bone
  4. secondary bone tumour is formed
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3
Q

What role do intravenous bisphosphanates play in managing secondary bone tumours?

A

to inhibit osteoclastic resorption of bone

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4
Q

What is the pathophysiology of osteosarcomas?

A
  1. malignant osteosarcomas arise from osteoblasts
  2. they secrete osteoid
  3. then local spread occurs quickly, destroying the cortex
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5
Q

How can you spot osteosarcoma on an X-ray?

A
  1. ill-defined lesion with an indistinct zone of transition
  2. sclerotic or lytic areas within the lesion
  3. cortical destruction
  4. codman triangle
  5. sunray spicules
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6
Q

What is the prognosis of osteosarcoma?

A
  • 5 year survival rate is 60%
  • prognosis better in adolescents
  • poor prognosis for elderly patients with pagets
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7
Q

Why are isotopic bone scans helpful investigations for osteosarcoma?

A

highlights areas of bony metabolic activity

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8
Q

How are osteosarcomas managed?

A
  • preoperative chemotherapy followed by limb salvage surgey
  • amputation occasionally required
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9
Q

What is codman triangle?

A

the triangular area of new subperiosteal bone that is created when a lesion raises the periosteum away from the bone.

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10
Q

How are secondary bone tumours managed conservatively?

A
  • analgesia
  • splintage
  • radiotherapy for bony metastatic pain
  • chemotherapy
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11
Q

what are the 6 tumours most likely to metastasize?

A
  1. breast
  2. lung
  3. prostate
  4. renal
  5. thyroid
  6. bowel
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12
Q

What is the most common malignant primary tumour?

A

Osteosarcoma

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13
Q

Why are bone biopsies not always performed when investigating osteosarcoma?

A

to avoid the risk of causing seeding in nearby tissues

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14
Q

What surgical management is available for secondary bone tumours?

A
  • intramedullary fixation of long bones for fracture (including in palliative care for pain relief)
  • joint arthroplasty
  • spinal decompression and stabilisation for acute cord compression
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15
Q

What is chondosarcoma?

A

a rare malignant primary bone tumour arising from chondrocyte cells

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16
Q

Where do osteosarcomas most commonly arise?

A
  • around the knee
  • proximal humerus
  • femur
17
Q

How are secondary bone tumours investigated?

A
  • blood tests to identify the primary (CEA or PSA etc.)
  • Plain X-ray (osteolytic, sclerotic or mixed lesions)
18
Q

Who are more likely to develop osteosarcoma?

A
  • under 20 years old
  • elderly with paget’s disease
19
Q

How are chondosarcomas managed?

A

wide excision of the lesion is sometimes possible

amputation may be only viable option

chemotherapy and radiotherapy are less effective

20
Q

How is the extent of osteosarcomas determined?

A

MRI or CT

21
Q

How do secondary bone tumours present?

A
  • bone pain in the axial skeleton
  • night pain that does not respond to simple analgesia
  • systemic symptoms
  • change in neurological signs corresponding to the specific spinal vertebral level affected
22
Q

What is the most common bone-destroying lesion in the older patient?

A

secondary bone tumours