viva questions Flashcards

(15 cards)

1
Q

what is osteosarcoma?

A

osteosarcoma is a primary bone tumour affecting metaphysis of the long bones like distal femur ( most common) , proximal tibia and proximal humerus.
it is characterised by production of immature bone ( osteoid) by tumour cells.

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2
Q

what are the common sites for osteosarcoma?

A

distal femur ( M.c) followed by proximal tibia , proximal humerus.

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3
Q

what is the typical age group of affected by osteosarcoma?

A

bimodal age group distribution:-
1) children and adolescents(10-25 years)
2) elderly ( > 40years):- secondary osteosarcoma( associated Paget’s disease , radiation, etc)

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4
Q

what are the classic radiographic features of osteosarcoma?

A

MAC Lamellar
1)mixed lytic and sclerotic lesion
2) aggressive periosteal reaction ( codman’s traingle, sunburst pattern)
3) Codman’s triangle:-elevation of the periosteum forming a triangular appearance.
4) lamellate( onion -skin) reaction:- Less common, seen in aggressive lesions.

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5
Q

how to differentiate osteosarcoma from Ewing’s sarcoma?

A

osteosarcoma:-
1) age gp- 10-25 years
2) location:-metaphysics
3) matrix mineralisation - present
4) soft tissue involvement :- common
5) periosteal reaction:- sunburst , cowman’s triangle

Ewing’s sarcoma:-
1)age group:- 5-20 years
2) location:- diaphysis
3)matrix mineralisation:- absent
4) soft tissue involvement:- common
5) periosteal reaction:-onion skin( lamellated pattern) due to repetitive periosteal lifting.

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6
Q

what are the characteristic MRI findings of osteosarcoma?

A

LOW T1, HIGH T2 signal intensity.
HETEROGENOUS POST contrast enhancement
SOFT TISSUE EXTENSION with peritumoral edema
SKIP LESIONS( satellite nodules in bone marrow)

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7
Q

how does osteosarcoma appear on a ct scan ?

A

better visualisation odf destruction and mineralised matrix.

soft tissue involvement
calcification within the timor.

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8
Q

what is the role of pet-ct in osteosarcoma ?

A

1) detects distant mets( esp lungs)
2) assesses metabolic activity of the tumour.
3) monitors to chemotherapy.

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9
Q

how do you stage osteosarcoma?

A

enneking staging system( for bone tumour)

stageI:-low-grade, no mets
stageII:-high grade, no mets
stageIII:-metastatic disease.
AJCC TNM staging is also used.

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10
Q

what is the most common site for metastases in osteosarcoma?

A

LUNGS( most common)
BONE( Second most common)

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11
Q

how do lung mets look like on a chest X-ray and ct scan?

A

multiple round “ cannon ball” opacities.
Ct scan :- well defined nodules. sometimes calcified.

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12
Q

differential diagnosis for aggressive bone lesion in a young patient?

A

ECOOL
E:- Ewing’s sarcoma
C:- chondrosarcoma ( in older patient)
O:-osteomyelitis
O:-osteosarcoma
L:-langerhans cell histiocytosi

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13
Q

what is the difference between conventional osteosarcoma and parosteal osteosarcoma?

A

CONVENTIONAL OSTEOSARCOMA

location:- intramedullary
growth:- aggressive, destructive
prognosis:- poorer
periosteal reaction:- sunburst, codman’s triangle.

PAROSTEAL OSTEOSARCOMA

location:-surface of the bone
growth :-slow growing
prognosis:-better
periosteal reaction:-thick, lobulated

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14
Q

what is the imaging features of telangiectatic osteosarcoma?

A

LYTIC LESION with fluid -fluid levels on MRI( due to blood -filled spaces)
MINIMAL MATRIX mineralisation
HIGHLY AGGRESSIVE with cortical destruction.

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15
Q

what is the significance of tutor necrosis percentage on imaging?

A

> 90% :- necrosi post -chemotherapy - good prognosis

<90% necrosis:- worse prognosis, poor response

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