Musculo-skeletal soft tissue tumours Flashcards

1
Q

what do soft tissue tumours often present as

A

a lump or swelling

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2
Q

what may soft tumours be associated with

A

pain or discomfort

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3
Q

are superficial lesions more or less likely to be malignant

A

less likely

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4
Q

what is a ganglion cyst

A

a lump found near a joint capsule or tendon sheath

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5
Q

what part of the body do ganglion cysts often arise

A

the wrist

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6
Q

what changes are seen in a ganglion cyst

A

degenerative change within the connective tissue and secondary inflammatory changes

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7
Q

what is seen histologically in ganglion cysts

A

a space with myxoid material

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8
Q

is a ganglion a true cyst, and why/why not

A

no not a true cyst because it has no epithelial lining

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9
Q

describe the pathology seen with nodular fasciitis

A

cellular proliferation of fibroblastic and myofibroblastic cells

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10
Q

what are some properties of nodular fasciitis

A

self limiting disorder and a rapidly growing tumour

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11
Q

what group of people is nodular factiitis usually seen in

A

young adults, history of trauma in 25% cases

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12
Q

what histological changes are seen in nodular fasciitis

A

stellate + spindle tissue culture appearance, haemorrhage, mitosis and increased plump cells

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13
Q

what other tumour is similar to nodular fasciitis

A

myositis ossificans

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14
Q

what is there usually a history of in myositis ossificans

A

trauma

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15
Q

what is myositis ossificans associated with

A

insertions of large muscles of arms and legs

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16
Q

what pathology is seen with myositis ossificans

A

cellular proliferation but with evidence of bone formation and zonation
(recognition of organisation is critical)

17
Q

what group of people is superficial fibromatoses most commonly seen in

A

men > women, average age 60

common

18
Q

what condition is superficial fibromatoses associated with

A

Dupuytren’s

19
Q

describe the cause of superficial fibromatoses

A

idiopathic

associated with alcohol, diabetes and anticonvulsants

20
Q

describe the pathology seen in Dupuytren’s

A

firm grey-white tissue, nodules + fascicles, bland fibroblasts, dense collagen

21
Q

describe deep fibromatoses

A

desmoid tumour, large infiltrative masses that do not metastasise

22
Q

what group of people is deep fibromatoses often seen in

A

often young adults, teen to 30s

23
Q

what sites does deep fibromatoses involve

A

musculo-aponeurotic tissue of abdominal wall, mesenteric tissue, limb girdles

24
Q

what are the 2 different types of tenosynovitis

A

giant cell tumour of tendon sheath and pigmented villonodular synovitis
(similar histology)

25
Q

what parts of the body does giant cell tumour of the tendon sheath involve

A

the digits and wrist

26
Q

what joints does pigmented villonodular synovitis affect

A

large joints

27
Q

what pathology is seen with giant cell tumour of tendon sheath

A

reactive proliferation

28
Q

describe the recurrence of the different types of tenosynovitis

A

giant cell tumour of tendon sheath = excise, rarely recurs

pigmented villonodular synovitis = more likely to recurt

29
Q

what is the nomenclature of benign and malignant soft tissue tumours

A
benign = oma
malignant = sarcoma
30
Q

what are the grading features of sarcomas

A

degree of differentiation, degree of proliferation(mitotic count), presence of coagulative necrosis