Bone tumours Flashcards

1
Q

Malignant bone tumours

A

Multiple myeloma (most common)
Osteosarcoma
Ewing’s sarcoma
Chondrosarcoma

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2
Q

Benign bone tumours

A

Osteochondroma (most common)
Osteoid osteoma
Chondroma
Fibrous dysplasia of bone

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3
Q

Bone sarcoma presentation

A

Non-mechanical bone/joint pain
Bone pain at night
Bony swellings
Pathological fractures

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4
Q

Multiple myeloma defining feature

A

Multiple punched out osteolytic lesions on radiography

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5
Q

Osteosarcoma presentation

A

1˚ Typically adolescents in metaphyses of long bones, especially knee
2˚ often follows irradiation/Paget’s disease adolescents
Pt presents with pain first, 50% tend to be knee

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6
Q

Osteosarcoma imaging findings

A
Sunray spiculation (bone destruction + new forming)
Periosteal elevation (Codman's triangle)
Staging uses intramedullary spread with MRI + CT for metastases
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7
Q

Osteosarcoma treatment + prognosis

A

Neoadjuvant chemo prior to surgery

60-70% 5yr survival

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8
Q

What is Ewing’s sarcoma

A

Round-cell tumour of long bones (typically diaphysis) + limb girdles, presents in adolescents

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9
Q

Ewing’s sarcoma XR features

A

Bone destruction
Onion ring sign (new bone forming in concentric layers)
Soft-tissue swelling
Periosteal elevation (Codman’s triangle)

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10
Q

Ewing’s sarcoma treatment + prognosis

A

Chemo, surgery + radiotherapy required

55% 5yr survival if no mets, 22% with mets

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11
Q

Chondrosarcoma causes

A

de novo or from chondroma malignant transformation

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12
Q

Chondrosarcoma presentation

A

Pain/lump on axial skeleton of middle aged

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13
Q

Chondrosarcoma imaging

A

XR shows popcorn calcification

MRI/CT for extent of tumour

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14
Q

Chondrosarcoma treatment

A

No response to chemo/radiotherapy

Surgical excision is only therapy, local recurrence if inadequate surgery

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15
Q

Limb-sparing surgical reconstruction

A

Replacement of excised bone tumour with metal/polyethylene endoprosthesis/bone allograft as alternative to amputation
85% of pts have limb salvaged following chemotherapy for 1˚ bone tumours

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16
Q

Osteochondroma presentation

A

Usually affects knee, proximal femur/humerus

Presents as painful mass associated with trauma

17
Q

Osteochondroma imaging

A

Xray shows bony spur arising from cortex, usually pointing away away from joint

18
Q

Osteochondroma treatment

A

Remove if causing symptoms (e.g. pressure on other structures)
Remove if growing after skeletal maturity - malignancy risk

19
Q

Osteoid osteoma presentation

A

Painful benign bone lesion, occurs mainly in long bones/spine of 10-25 yr old males
Nidus of osteoid osteoma produces prostaglandins which causes pain unrelated to activity

20
Q

Osteoid osteoma imaging

A

Local cortical sclerosis on XR with central radiolucent nidus (central area), which may contain small calcified area
Plain XR may miss these tumours, CT is best

21
Q

Osteoid osteoma treatment

A

Prostaglandin inhibitors e.g. ibuprofen

CT guided biopsy + radiofrequency ablation

22
Q

What is a Chondroma

A

Benign cartilagenous tumour arising from bone surfaces/medulla (enchondromata if within medulla)
Causes local swelling/#

23
Q

Chondroma treatment

A

Rarely needed unless malignant (chondrosarcoma)

24
Q

What is fibrous dysplasia of bone + complications

A

Developmental abnormality where bone incorrectly formed

May cause pain/inc risk of #

25
Q

Fibrous dysplasia of bone treatment

A

Surgical stabilisation may be needed

In polyostic form bisphospanates may help with symptoms

26
Q

Sarcoma vs carcinoma

A

Sarcoma is malignant neoplasm arising from mesenchymal cells (connective + non-epithelial tissue)
Carcinomas affect epithelial tissues

27
Q

Any soft tissue lump considered to be malignant soft tissue sarcoma if

A
Any one from:
Bigger than 5cm
Increasing in size
Deep to deep fascia
Painful
28
Q

Soft tissue sarcoma imaging

A

MRI then needle biopsy

Pathological diagnosis + gene expression profiling to target chemo

29
Q

Soft tissue sarcoma treatment

A

Excision with wide margins, then radiotherapy

Adjuvant chemotherapy with doxorubicin/trabectedin

30
Q

Soft tissue sarcoma prognosis

A

Related to histological grade, size, depth of tumour
<50% 5yr survival for high-grade large deep
Children respond better to chemo, higher survival rate