Lec 16 Bone Tumor Flashcards

(39 cards)

1
Q

What are of bone most likely to have infection/tumor?

A

metaphysis

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2
Q

Who gets an osteoid osteoma?

A

young adults < 25 yo; M > F

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3
Q

What is location of osteoid osteoma?

A

in cortex of long bones

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4
Q

What are characteristics of osteoid osteoma?

A
  • benign, sharply demarcated osteoblastic
  • < 2 cm in size
  • pain at night relieved by aspirin
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5
Q

What is most common primary bone malignancy?

A

osteosarcoma

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6
Q

What are characteristics of osteosarcoma?

A
  • tumor produces bone matrix

- present w/ pain, swelling, pathologic fracture, high alkaline phosphatase

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7
Q

Who gets osteosarcoma?

A

young adults < 20; smaller peak after age 50

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8
Q

What is location of osteosarcoma?

A

near sites of active bone growth = metaphysis

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9
Q

Where does osteosarcoma metastasize?

A

hematogenously to lungs

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10
Q

What is treatment for osteosarcoma?

A

pre-op chemo + surgery

good prognosis

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11
Q

What are characteristics of osteochondroma?

A
  • most common benign bone tumor
  • can be solitary or multiple
  • neoplastic lateral outgrowth from growth plate w/ cartilaginous cap
  • rarely transforms to chondrosarcoma
  • synchronously grows w/ normal epiphyseal growth plate; stops growing when skeletal maturity reached
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12
Q

Who gets osteochondroma?

A

males < 25 yo

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13
Q

What is osteochondromatosis?

A

familial disorder with multiple hereditary osteochondromas

autosomal dominant
have asymmetric retardation of longitudinal bone growth

manifests in adolescence and ceases in adulthood

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14
Q

What is an enchondroma?

A

benign intramedullary hyaline cartilage neoplasm

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15
Q

Where does enchondroma occur?

A

appendicular skeleton in medullary region

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16
Q

What are characteristics of enchondroma?

A
  • variable presentation: aysmptomatic, painless swelling

- can resemble chondrosarcoma

17
Q

What is enchondromatosis [ollier disease]?

A

rare non hereditary disorder of multiple intramedullary cartilaginous tumors

affected limb may be shortened or deformed; rarely progresses past puberty

may develop assocaited chondrosarcoma or osteosarcoma

18
Q

What is maffucci syndrome?

A

enchondromatosis + hemangiomas

increased susceptibility to development of sarcoma

19
Q

What is chondrosarcoma?

A

malignant mesenchymal tumor of malignant cartilaginous cells

can be primary or arise from previous enchondroma or osteosarcoma

20
Q

Where is chondrosarcoma located?

A

in medullary cavity

21
Q

Who gets chondrosarcoma?

A

men 30-60 yo [peak 55]

22
Q

What is treatment for chondrosarcoma?

A

does not respond to chemo –> must remove surgically

23
Q

What do you see in ewing sarcoma radiographically?

A
  • destructive lytic lesion

- onion skin periosteal reaction

24
Q

Who gets ewing sarcoma?

A

10-15 yo; M > F

caucasians

25
Where is ewing sarcoma located?
diaphysis of long bones
26
What are characteristics of ewing sarcoma?
have pain in area, fever, sick = mimics osteomyeltis warm, enlarging mass from neuroectoderm --> mesenchymal cells = small round blue cel tumor; no matrix production
27
What is treatment for ewing?
chemo, radiation, surgery
28
What is a fibrous cortical defect?
non neoplastic intracortical proliferation of fibrous tissue and histiocytes seen in kids M > F in metaphysis
29
What is a non-ossifying fibroma?
fibrous cortical defect 2-5 cm in adolescents expanded into medullary cavity may present w/ pathologic fracture
30
What do you see on xray with non ossifying fibroma?
well circumscribed lytic lesion with slightly sclerotic rim | in metaphysis
31
What is monostotic fibrous dysplasia?
single bone fibrous dysplasia | stops when growth plate closes
32
What is fibrous dysplasia?
benign fibroosseus tumor | intramedullary proliferation of fibrous tissue + woven bone --> failure to differentiate to mature bone
33
Who gets fibrous dysplasia?
age < 30 yo [kids and young adults]
34
What are 3 types of fibrous dysplasia?
monostotic = single bone polystotic = multiple bones mccune albright syndrome = polyostotic FD + endocrine abnormalities [precocious puberty] + cafe au lait spots
35
What are signs of mccune albright syndrome
polyostotic FD + endocrine abnormalities [precocious puberty] + cafe au lait spots
36
What happens in polyostotic fibrous dysplasia?
present in young pts than monostotic; continues into adulthood have craniofacial invovlement often
37
What is a giant cell tumor?
benign locally aggressive; usually solitary tumor around knee
38
Who gets a giant cell tumor?
20-40 yo
39
Where is giant cell tumor located?
epiphysis