Bone tumours Flashcards

(53 cards)

1
Q

top 5 primary tumours that metstasise to bone

A

breast

prostate

lung

kidney

thyroid

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2
Q

common non-malignant tumours of bone and soft tisseu 3

A

enchondromas

osteochondroma

lipoma

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3
Q

how do myeloma and lymohas present 1

A

usually with MSK pain

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4
Q

red flag syx assoc w MSK malignancy in adults 4

A

night pain

unremitting pain

non-traumatic joint of limb pain

weight loss

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5
Q

Mx of malignant secondary bone lesions 7

A

Mx-range of oncology options:
-chemo
-radio (internal and external)
-mAB
-bisphosphonates
-surgery
-injecting bone cement into bones
-pain control

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6
Q

IX for secondary bone tumours 2

A

MRI and PET-CT

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7
Q

common sites of bone metastis that cause pain 4

A

spine

pelvis

hips

long bones

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8
Q

which primary bone tumour is more common in children

A

sarcoma

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9
Q

where do osteosarcomas present

A

in the metaphyseal portion of the bone

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10
Q

common presenation of sarcoma 4

A

limping child

progressive swelling around the knee

any progressive limb swelling

night pain

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11
Q

most common primary malignant bone tumour

A

multiple myeloma
-accounts for 45%

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12
Q

hallmark bone manifestation of multiple myeloma 1

A

multiple punched-oout osteolytic lesions

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13
Q

2nd most common primary malignant bone tumour

A

osteosarcoma

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14
Q

who gets primary osteosarcomas and where

A

typically adolescents
-aries in the metaphysis of the long bone (esp the knee)

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15
Q

who gets secondary osteosarcomas and where

A

typically 10-20yrs w peak in adolescent growth

-arises in bones affected by Pagets disease or post-irridation

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16
Q

difference between primary and secondary osteosarcoma

A

Primary osteosarcoma, originates in bone cells and is not directly associated with another cancer or disease.

Secondary osteosarcoma also originates in bone cells but is associated with either a skeletal disease or treatment from another condition (typically cancer

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17
Q

x-ray findings in osteosarcoma 2

A

bone destruction and new bone formation- sunburst pattern [45]

marked periosteal elevation- Codsmans tirangle [46]

(50%. of lesions around the knee)

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18
Q

what other imaging can be used in osteosarcoma diagnosis and why 2

A

staging MRI- assess for intramedullary spread

HRCT chest (high resolution)
-screen for lung mets
-ESP if raised ALP

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19
Q

treatment for osteosarcoma 2

A

historically limp amputated
-still has 80% recurrence rates
-try and do limb salvage surgery

neoadjuvant chemo (prior to surgery)

standard therapy is limb salvage surgery and neoadjuvant chemo

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20
Q

predisosing factors for osteosarcoma 3

A

mutations of Rb gene (hence assoc w retinoblastoma)

Pagets disease of the bone

radiotherapy

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21
Q

define ewings sarcoma

A

malignant round-cell tumour of long bones (diaphysis) and limb girdles

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22
Q

who gets ewings sarcoma

A

typically adolescents

23
Q

what genetic abnormality is commonly seen in ewings sarcoma

A

T11:22 chromosomal translocation

24
Q

radiological features of ewings sarcoma 4

A

bone destruction

new bone formation in concentric layers- ‘onion ring’ sign [47]

soft tissue swelling

periosteal elevation

25
treatment for ewings sarcoma 3
chemo surg radio
26
key adverse prognositc factor for ewings sarcoma 1
mets at diagnosis
27
what can cause chondrosarcoma 2
can be de novo or from malignant transformation of chondromas (cartilage tumours)
28
what is chondrosarcoma assoc with 2
pain and a lump
29
who gets chondrosarcoma
common in middle age
30
where is affected by chondrosarcoma
axial tumour
31
typical xray appearance of chondrosarcoma
popcorn calcifacation [48] -(MRI/CT will better define tumour extent)
32
treatment for chondrosarcoma 1
has no response to radio/chemo treatment is excision
33
commonest benign bone tumour
osteochondroma
34
where does osteochondroma typically present 3
above the knee proximal femur humerus
35
presentaion of osteochondroma 2
painful mass associated with trauma
36
x-ray appearance of osteochondroma
bony spur arising from cortex & usually pointing away from joint
37
treatemtn for osteochondroma 2
remove if causing syx any tumour continuing to grow after skeletal maturity must be removed
38
what condition predisposes patients to osteochondroma -inheritance pattern? -appearance -risk
hereditary muoltiple exostoses -Autosomal dominant -causes short stature and forearm, ankle and knee deformity up to 10% of osteochondroma will become malignant in these patients
39
who gets osteochondroma
male <20yr
40
define osteoid osteoma
painful benign bone lesion
41
who gets osteoid osteoma and where
most commonnly in long bones (can also occur in spine) and males 10-25yo
42
appearance of osteoid osteoma on xray
local cortical sclerosis on XR -w central radiolucent nidus[49] -within nidis can be a small nuclear of calcification -
43
define nidus
the centre of an osteoid osteoma -consists of growing tumour cells, bld vsls and osteoblasts/clasts
44
what causes the pain in osteoid osteoma
the nidus releases prostaglandins that cause pain unrelated to activity
45
treatement for osteoid osteoma 2
ibuprofen relieves pain caused by the nidus CT guided biopsy and radio-frequency ablation (plain XR may miss these allwasy CT)
46
define chondromas
benign cartilaginous tumours arising from bone surfaces
47
define enchondromata
a chondromas within the medulla
48
presenation of chondromas
may cause local swelling or fracture
49
Mx of chondromas 1
rarely needed exclude conversion ot malignancy (chondrosarcoma)
50
define giant cell tumour
bening tumour of multinucelated giant cells within a fibrous stroma
51
peak incidence of giant cell tumour
20-40
52
where do giant cell tumour appear
epiphyses of long bones
53
appearance of giant cell tumour on XR
double bubble or soap bubble appearance [50]