Bone Tumours Flashcards

1
Q

what is the most common primary tumour of bone marrow?

A

multiple myeloma

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2
Q

what is multiple myeloma?

A

a tumour that forms in the white cells of the bone marrow

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3
Q

who is generally affected by multiple myeloma?

A

elderly patients

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4
Q

what cancers commonly spread to bone?

A
breast 
lung 
prostate 
renal 
thyroid
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5
Q

when are primary bone sarcomas more common?

A

childhood

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6
Q

what are the risk factors for primary bone cancers?

A

previous radiotherapy
predisposing conditions
genetic conditions

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7
Q

what are the three predisposing conditions for primary bone cancers?

A

Paget’s disease
fibrous dysplasia
multiple enchondromas

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8
Q

what genetic conditions increase risk of primary bone tumours?

A

li fraumeni

familial retinoblastoma

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9
Q

what age group is most commonly affected by primary bone tumours?

A

10-30

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10
Q

how does a primary bone tumour present?

A

persistent pain
swelling and erythema
palpable mass
pathological fracture

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11
Q

describe the pain associated with primary bone tumours

A

worse at night
well localised
doesn’t respond well to analgesia

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12
Q

when do primary bone tumours cause pathological fractures?

A

if they have caused loss of bone

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13
Q

what investigations are done for primary bone tumours?

A

x-rays
CT
MRI
bone scan

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14
Q

what are the neoadjuvant treatment options for primary bone tumours?

A

chemotherapy
radiotherapy
hormone therapy

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15
Q

what is the aim of Neo adjuvant therapy in primary bone tumours?

A

shrink tumour before surgery

reduce risk of metastasis

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16
Q

what surgery can be done for primary bone tumours?

A

excision and reconstruction

amputation

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17
Q

what adjuvant treatment may be done for primary bone tumours?

A

chemotherapy

radiotherapy

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18
Q

what is the most common malignant tumour of bone?

A

osteosarcoma

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19
Q

what age group is affected by osteosarcoma?

A

children

young adults

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20
Q

what is the second peak of osteosarcoma?

A

elderly patients with Paget’s

21
Q

where does osteosarcoma usually affect?

A

around the knee

22
Q

how do around a fifth of patients with osteosarcoma present?

A

with pulmonary metastases

23
Q

how is osteosarcoma managed?

A

chemotherapy

limb salvage

24
Q

who gets Ewing’s sarcoma?

A

5-25 years old

25
where is Ewing's sarcoma usually found?
diaphsysis of long bones
26
what is the prognosis of Ewing's sarcoma?
70% if localised | 30% if metastatic
27
how is Ewing's sarcoma managed?
chemo limb salvage +/- radiotherapy
28
is Ewing's sarcoma benign or malignant?
malignant
29
what is chondrosarcoma?
malignancy of chondrocytes
30
who gets chondrosarcoma?
older patients (40-75)
31
where is chondrosarcoma commonly found?
pelvis | femur
32
describe the appearance of chondrosarcoma on x-ray
lytic/blastic lesions with cortical thickening
33
is osteoid osteoma benign or malignant?
benign
34
where is osteoid osteoma usually found?
long bones
35
who gets osteoid osteoma?
young people (5-25)
36
how does osteoid osteoma present?
pain that is worse at night and relieved by aspirin
37
when do osteoid osteomas get better?
spontaneously after 6-18 months
38
what management can be done for osteoid osteoma?
radiofrequency ablation
39
what is the most common benign bone tumour?
osteochondroma
40
what is an osteochondroma?
a benign lesion formed from abnormal cartilage
41
when do multiple osteochondromas occur?
in hereditary multiple exostoses (HME)
42
who gets osteochondroma?
common in young people
43
how can osteochondroma be managed?
excised if causing symptoms
44
what is an enchondroma?
a benign intramedullary cartilage lesion
45
who gets enchondromas?
20-50 year olds
46
how does an enchondroma present?
asymptomatic | usually an incidental finding
47
how is enchondroma managed?
conservative usually curettage and bone grafting if symptomatic
48
what does it mean if a lesion is lytic?
loss of bone
49
what does it mean if a lesion is sclerotic?
gain of bone