Tumours of unknown origin Flashcards

1
Q

what is Ewing’s sarcoma

A

a malignant bone tumour

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2
Q

what bones does Ewing’s sarcoma usually affect

A

diaphysis of long bones(femur) and pelvic bones

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3
Q

what are the clinical features of Ewing’s sarcoma

A

painful enlarged masses, site is swollen, tender and warm

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4
Q

what is seen in radiology of Ewing’s sarcoma

A

destructive lesion that involves the surrounding tissue and reactive bone that gives onion skin appearance

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5
Q

what is seen histologically in Ewing’s sarcoma

A

primitive round cells, no obvious lines of differentiation

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6
Q

describe the behaviour of Ewing’s sarcoma

A

aggressive

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7
Q

what treatment is used for Ewing’s sarcoma

A

neoadjuvant chemotherapy and surgery +/- radiotherapy

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8
Q

describe the pathology of Synovial sarcoma

A

deep seated mass, not of synovial origin

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9
Q

where in the body does Synovial sarcoma usually affect

A

around knee joint, chest wall, head and neck areas

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10
Q

what group of people does synovial sarcoma usually affect

A

patients 20-40 years old

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11
Q

what does it mean if synovial sarcoma is biphasic

A

combines areas of spindle cells and epithelial cells

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12
Q

what does it mean if synovial sarcoma is monophasic

A

only one form(cell type) present, usually spindle cells

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13
Q

describe the spread of synovial sarcoma

A

can metastasise, to lungs or regional lymph nodes

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14
Q

describe how synovial sarcoma is treated

A

treated aggressively, with surgery +/- chemotherapy

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15
Q

what area of the body does undifferentiated pleomorphic sarcoma affect

A

deep soft tissue of extremities, usually thigh

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16
Q

describe the usual size of undifferentiated pleomorphic sarcoma

A

large(10-20cm)

17
Q

describe the pathology of undifferentiated pleomorphic sarcoma

A

areas of necrosis + haemorrhage, high grade cytology, pleomorphic cells

18
Q

describe the behaviour of undifferentiated pleomorphic sarcoma

A

aggressive

19
Q

describe what giant cell tumour(osteoclastoma) is

A

a benign but locally aggressive tumour

20
Q

what age group is giant cell tumour(osteoclastoma) usually seen in

A

20s to 40s

21
Q

where do giant cell tumours(osteoclastoma) usually arise

A

in the epiphysis of the femur and tibia

22
Q

what symptoms can giant cell tumours cause

A

arthritis like symptoms or fracture

23
Q

describe the pathology of giant cell tumours(osteoclastoma)

A

often destroy cortex and expand into soft tissue, thin shell of reactive bone, can become cystic

24
Q

what treatment is used for osteoclastoma and for aneurysmal bone cysts

A

curettage

25
Q

what age group do aneurysmal bone cysts usually affect

A

can be any age group, usually in first 2 decades

26
Q

what do aneurysmal bone cysts arise from

A

metaphysis of long bones and posterior elements of vertebral bodies

27
Q

what symptoms do aneurysmal bone cysts cause

A

pain and swelling

28
Q

what is seen on radiology of aneurysmal bone cysts

A

eccentric, expansile, lytic lesion with smooth margin and thin shell of bone

29
Q

what is an aneurysmal bone cyst tumour formed of

A

multiloculated blood filled spaces