Bone and Soft Tissue Tumors Flashcards

1
Q

What are the 18 and 2* ossification centers?

A

metaphysis and epiphysis

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2
Q

What are the 4 adult soft tissue sarcomas?

A

UPS/MFH
liposarcoma
leiomyosarcoma
angiosarcoma

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3
Q

What are the 3 soft tissue tumors of children? How do they metastasize?

A

rhabdomyosarcoma
synovial sarcoma
epithelioid sarcoma

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4
Q

How are benign soft tissue tumors characterized?

A

small, slow growing, well-circumscribed and homogenous surface

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5
Q

How are malignant soft tissue tumors classified?

A

large, hemorrhagic, necrotic, rapid growing, poorly cirumscribed, heterogenous surface

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6
Q

What are the prognostic factors for soft tissue tumors?

A

stage- most important
grade
size
location- superficial and peripheral are better than deep and central

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7
Q

What does the prognostic factor of grade indicate?

A

degree of differentiation

low-> high determined by amt of mitosis, cellularity, pleomorphism, necrosis

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8
Q

What is the histological appearance of low grade vs high grade fibrosarcoma?

A

low: elongated spindle cells, fat, pink collagen, limited mitosis and no necrosis
high: hypercellularity, mitotic figures, unorganized

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9
Q

What are the common routes of metastasis for soft tissue sarcoma?

A

lung via blood

lymphatics

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10
Q

What are the treatments for soft tissue sarcomas?

A

radiation
surgery
chemotherapy- only for some pediatric cases usually

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11
Q

What are the 3 most common soft tissue tumors?

A

MFH
liposarcoma
synovial sarcoma

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12
Q

What are some differential diagnoses for small round blue cell tumors in bone?

A

Ewings, osteosarcoma, lymphoma/leukemia, neuroblastoma, chondrosarcoma

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13
Q

What are some of the differential diagnosis for small round blue cell tumors of soft tissue?

A

Ewings, rhabdomyosarcoma, round cell liposarcoma, mesenchymal chondrosarcoma, synovial sarcoma

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14
Q

If you suspect a bone tumor in an adult, what is the generalization until proven otherwise?

A

MM or metastatic disease

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15
Q

What is the treatment for osteosarcoma?

A

pre-op chemo, surgery resection, post-op chemo

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16
Q

what is the treatment for Ewings?

A

chemo, possibly: surgery resection, radiation

17
Q

What are the primary sites for skeletal metastases?
Osteoblastic? *
Osteolytic?

A

PTBLK- adults
prostate*, thyroid, breast, lung, kidney
children- neuroblastoma and wilms tumor

18
Q

Which bones are commonly metastasized too first?

A

skull, vertebrae, pelvis

tubular bones are more rarely met to.

19
Q

What are the clinical manifestations of bone mets?

A

pain, pathological fractures and marrow dysfunction

20
Q

Giant cell tumors most commonly occur where, what ages and gender?

A

males/females, 30s, knee/wrist

21
Q

Osteosarcoma is characterized by what?

A

malignant tumor of direct bone/osteiod formation by proliferating tumor cells

22
Q

What is the radiographic presentation of osteosarcoma?

A

fluffy osteoid, codman’s triangle, and cortical destruction mass

23
Q

How is chondrosarcoma characterised? Radiographic presentation?

A

men, 50s, knee/hip
popcorn/smoke ring appearance on xray
Bx: see cartilage on bone bx of adult (not nl)

24
Q

What is the epidemiology of ewings sarcoma?

A

boys, 10-12 yrs, white, femur/hip, chromosomal abl of t(11;22)

25
Q

What is the clinical differential diagnosis of bone tumor with potential Ewings?

A

Osteomyelitis v tumor-Ewings Sarcoma

26
Q

What is the radiographical appearance of Ewing’s Sarcoma?

A

onion-skinning periosteal reaction, permeative destruction, diphyseal

soft tissue mass on CT and MRI