Bone Tumours Flashcards

1
Q

What are the Primary bone tumours ?

A

Bone - osteosarcoma
Cartilage - chondrosarcoma
Fibrous tissue - fibrosarcoma
Bone marrow - Ewing’s sarcoma, myeloma
Vascular - angiosarcoma
Uncertain - malignant giant cell tumour

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2
Q

What is an osteosarcoma?

A

Malignant osteoblasts
Usually presents in children
Usually due to Paget’s in >40s

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3
Q

What are the risk factors for osteosarcoma? (3)

A

Paget’s
Familial retinoblastoma
Radiation

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4
Q

Wat are the clinical signs and investigations for osteosarcoma?

A

Pain and swelling around bone
Common in knee, humerus and femur
X-ray : bone expansion with surrounding soft tissue, possible pathological fracture, sunburst bone appearance, Codman’s triangle
MRI, CT and possible biopsy

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5
Q

What is the management for osteosarcoma?

A

Surgical excision
Radio/chemotherapy
Amputation

Good prognosis in young but poor in elderly (espc with Paget’s)

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6
Q

What is a chondrosarcoma?

A

Malignant chondrocytes
More common in males in 40s

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7
Q

What are the clinical signs and investigations for chondrosarcoma?

A

Malignant tumour producing cartilage
Pain and swelling
Mainly in axial skeleton, shoulder and ribs
X-ray : lytic lesion with central calcification and cortical destruction
CT or MRI

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8
Q

What is the management of chondrosarcoma?

A

Resistant to chemo/radiotherapy
Surgical excision possible before metastasise
Possible amputation
Good prognosis when low grade tumour

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9
Q

What is Ewing’s sarcoma?

A

Malignant bone marrow cells
Almost exclusively in under 40s
Tumour cells derived from neuroectoderm cells

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10
Q

What are the clinical signs and investigations fo Ewing’s sarcoma?

A

Small, round, and blue tumour cell appearance
Pain, swelling, fever
X-ray - onion skin periosteum, diaphysis of long bones

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11
Q

What is the management of Ewing’s sarcoma?

A

Surgical excision
Possible preoperative chemo/radiotherapy
Good prognosis before metastasis

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12
Q

What are metastatic tumours?

A

Malignant cells from other parts of the body - commonly prostate, breast, lungs, kidneys, thyroid.
Usually osteolytic (except prostate which is osteoblastic)
Secondary bone tumour
Most common in older pts

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13
Q

What are the clinical signs and investigations for metastatic bone tumours?

A

General or local progressive pain
Pain from acute pathological fracture
Symptoms of spinal cord compression
Systemic - weight loss, anorexia
Check ESR, CRP and WCC for possible infection
X-rays to determine whether it is osteolytic or sclerotic lesion

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14
Q

What is the management for metastatic bone tumours?

A

Treatment depends heavily on age and primary tumour
Pain - analgesia, bisphosphonates, focal radiotherapy, DXT, surgery
Orthopaedic treatment - intramedullary nails , joint replacement, plate/screw constructs, cement augmentation - all ways to achieve skeletal integrity and stabilise abnormal bone which my be causing symptoms at risk of fracture.

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15
Q

How does metastasise occur?

A

Complex series of steps
Endothelial progenitor cells essential to lead to angiogenesis
Induce osteoclasts
Osteoblastic response variable depending on tumour cell

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16
Q

What to ask in pt history ?

A

Bone pain
Red flags - e.g weight loss
Symptoms from primary if diagnosed first
Function impairment - bc of pain, difficult moving affected limb, difficulty performing certain actions
Co-morbidities and pt expectations and understanding
Social circumstance - support?
Previous diagnosis of cancer and chemo?

17
Q

Why is using a CT good?

A

Structure
Good for pelvis and abdominal mets (3D)
Screening of chest/abdonmen and pelvis

18
Q

Why is using an MRI good?

A

Defines soft tissue involvement
Essential in spinal disease
SeeSkip lesions in long bones
Evaluation of suspected primary bone turnovers