Osteosarcoma (Complete) Flashcards

1
Q

Define osteosarcoma

A

Type of primary malingant bone tumor

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2
Q

Osteosarcomas are derived from what type of cells?

A

Mesenchymal cells

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3
Q

How common is osteosarcoma compared to other bone cancers?

A

Most common primary bone tumour in children and adolescents

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4
Q

Osteosarcoma is more common in which sex?

A

Male

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5
Q

What are the main risk factors for osteosarcoma?

A

Radiation exposure or chemotherapy

Genetic conditions:
* Li-Fraumeni Syndrome
* Retinoblastoma
* Rothmund-Thomson Syndrome

Chronic osteomyelitis

Bone infarcts

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6
Q

Name 3 genetic syndromes associated with increased risk of osteosarcoma

A

Li-Fraumeni Syndrome

Retinoblastoma

Rothmund-Thompson Syndrome

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7
Q

Define Li-Fraumeni Syndrome

A

Hereditary condition affecting tumor suppesor protein which greatly predisposes individuals to cancer

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8
Q

What is Rothmund-Thompson Syndrome?

A

Autosomal reccesive condition affecting skin, bones, hair and teeth

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9
Q

What are the features of osteosarcoma within the following grades:

G1

G2

G3

A

G1: Low-grade (Cells similar to normal bone)

G2: High-grade, abnormal cells

G3: High-grade, cells very different to normal bone

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10
Q

What are the features of stage 1A osteosarcoma?

A

Tumor located in original bone <8cm across

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11
Q

What are the features of stage 1B osteosarcoma?

A

Located in original bone >8cm across

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12
Q

What are the features of stage 2 osteosarcoma?

A

Located in original bone but cells are high-grade

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13
Q

What are the features of stage 3 osteosarcoma?

A

Tumor spread to multiple places in original bone

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14
Q

What are the features of stage 4 osteosarcoma?

A

Tumor has spread outside of original bone

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15
Q

What are the main signs/symptoms of osteosarcoma

A

Demographic:

Young (Under 25)
Male

Prolonged bone pain

  • Progressively worsens over span of weeks/months
  • Worse at rest and at night

Bone swelling

  • Typical in long bones
  • Firm, warm, ocassionally tender to touch

Pathologic fracture

  • Difficulty weight bearing due to pain

Limitted range of motion

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16
Q

Bone pain in osteosarcoma can often be mistaken for?

A

Growing pains

17
Q

What are the most common locations for osteosarcoma to form?

A

Knee (60%)

Proximal humerus

18
Q

What differentials should be considered alongside osteosarcoma?

A

Ewing’s sarcoma

Chondrosarcoma

Lymphoma of bone

Non-ossifying fibroma

19
Q

How can Ewig’s sarcoma be differentiated from osteosarcoma?

A

Similar presentations however more likely to have constitutional sypmtoms (e.g. fever and night sweats)

Often presents with soft tissue mass on shaft of long bones versus knee

Elevated ESR and LDH more common vs osteosarcoma

Onion skin appearance on x-ray

Small rounds cells and CD99+ on histology

20
Q

How can chondrosarcoma be differentiated from osteosarcoma?

A

More likely to occur in adults (>40 years).

More likely to occur in pelvis, shoulder or ribs

Lytic lesions with fluffy calcifications on XR

Malignant chondrocytes vs mesenchymal cells on histology

21
Q

How can lymphoma of the bone be differentiated from osteosarcoma?

A

More likely to have constitutional symptoms and weight loss

22
Q

How can non-ossifying fibroma be differentiated from osteosarcoma?

A

Asymptomatic, radiolucent lesion often found incidentally on imaging

23
Q

What investigation should be ordered in patients with suspected osteosarcoma?

A

Urgent x-ray within 48 hours for any young person with unexplained bone pain or swelling

24
Q

What findings on x-ray are suggestive of osteosarcoma?

A

Sunburst appearance (New bony growth with periosteal reaction)

Codman’s triangle: Elevated periosteum

25
26
Why is ALP elevated in osteosarcoma?
Due to high bone turnover rates (increased osteoblastic activity)
27
What further investigations are done following findings on X-ray suggestive of osteosarcoma?
Full body CT: Check for metastases Bone biopsy: To confirm diagnosis
28
What histological findings on bone biopsy are suggestive of osteosarcoma?
Malignant mesenchymal cells Replacement of bone marrow with trabecular/cancellous/spongy bone ALP +ve (high bone turnover rate)
29
What is the management plan for patients with osteosarcoma?
First-line: Surgical resection Neodajudavant + adjuvant chemotherapy: For metastatic disease Radiotherapy: If tumor is unoperable Follow-up imaging: Assess for recurrence
30
What is the prognosis for patients with osteosarcoma?
Localised: 70% 5-year survival Metastatic: 20% 5-year survival
31
What are poor prognostic factors for patients with osteosarcoma?
Primary tumor Large tumor volume Axial or proximal extremity location High ALP or LDH