Tumors 2 Flashcards

1
Q

Osteoma:

A

Homogenously dense, painless mass

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2
Q

Common locations of OSTEOMA:

A

1-Calvarium
2-Paranasal sinuses (esp. ethmoid & frontal; NOT common in maxillary)
3-sometimes seen in Mandible (Gardner synd. =mult. osteomas + colonic polyposis

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3
Q

Gardner Syndrome:
aka?
is an __ dominant form of polyposis characterized by the presence of multiple __ in the __ together with tumors outside the colon.
The extracolonic tumors may include __ of the skull, __ cancer, __ cysts, Fibromas, as well as the occurrence of desmoid tumors in approx. __% of affected individuals.

A
  • aka: familial colorectal polypsis
  • Autosomal
  • polyps
  • colon
  • osteomas
  • thyroid
  • epidermoid
  • 15%
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4
Q

Osteoma projects from:

A

internal table of skull

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5
Q

Osteoma on Xray:

A

-typically

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6
Q

Osteoid Osteoma:

A

histologically, a collection of highly vascularized osteoid tissue and giant cells surrounded by reactive sclerosis of host bone

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7
Q

Osteoid Osteoma sites:

A
  • 50% in tibia and femur
  • 10% in spine (1 of 3 benign post. arch tumors)
  • in long bones, metaphyseal or diaphyseal
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8
Q
Osteoid Osteoma:
\_\_% of all benign primary bone tumors 
age:
sex:
clinical: classic=
typically long \_\_ of pain b4 dx. 
lesions may \_\_-\_\_ over months/years
treated w/\_\_ \_\_ resection
common recurrence if \_\_ not removed.
A
  • 11%
  • 90% dx b4 age 25
  • males>females 2:1
  • classic= “pain worse at night, relieved by aspirin”
  • long history
  • self-resolve
  • en bloc
  • nidus
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9
Q

Osteoid Osteoma on Xray:

A

-radiolucent nidus is the lesion (

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10
Q

Osteoid Osteoma is one of 3 primary bone tumors that predilicts the __ elements of the __.

A
  • posterior

- spine

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11
Q

Osteoblastoma:

A

histological twin to osteoid osteoma

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12
Q

Osteoblastoma clinical:

A
  • long hx of pain; typically mos./yrs.

- larger, more expansile lesion

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13
Q

Osteoblastoma sites:

& treatment:

A
  • 30-50% in posterior arch of spine
  • 30% in long bones (femur & tibia most common; diaphyseal/metadiaphyseal location)
  • treatment=surgical resection
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14
Q

Osteoblastoma Xray:

A
  • expansile, geographic lesion
  • may be big: 2-12 cm dia.
  • matrix lucent, but may have strippled calcification
  • often with sclerotic border and sharp transition zone
  • usually lacks reactive dense reactive sclerosis of osteoid osteoma
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15
Q

Osteosarcoma incidence:

A
  • second most common primary malignancy of bone

- 20% of all primary malignancies of bone

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16
Q

Osteosarcoma histological:

A

-spindle-shaped stromal cells, osteoid and intercellular collagenous material

17
Q

Osteosarcoma age & sex:

A
  • 75% of cases between 10-25 years

- 2:1 male>female

18
Q

Osteosarcoma characterized by:

& treatment:

A
  • local pain, often with enlarging mass, swelling and redness
  • treatment= elevated serum alkaline phosphatase
19
Q

Osteosarcoma subtypes:

A

“conventional” most common

  • parosteal
  • periosteal
  • multicentric
20
Q

osteosarcoma sites:

A

most common: knee and proximal humerus

-reported almost everywhere

21
Q

osteosarcoma location:

A
  • metaphysis

- rare (5-7%) in spine

22
Q

Osteosarcoma on Xray:

A

basic patterns:

  • 50% are sclerotic
  • 25% lytic
  • 25% mixed pattern
  • soft tissue mass with calcification and/or ossification
23
Q

Osteosarcoma on Xray, periosteal reaction:

A

classically:

  • “sunburst”
  • “spiculated”
  • possible: permeative or moth-eaten bone lysis
24
Q

Osteosarcoma Treatment:

A

amputation + chemo

25
Q

Osteosarcoma survival:

A
  • survival rates were dismal (20%); recent improvement due to more effective meds
  • secondary osteosarcoma may develop from malignant degeneration of Paget’s, HME or following radiation therapy of benign lesion
26
Q

Osteosarcoma:

bone to bone __ is not common, but may occur.

A

-metastasis

multiple primaries rare, but reported- multi centric osteosarc