GCT, Osteochondroma, & Hemangioma Flashcards

1
Q

A giant cell tumor (GCT) is also called ____

A

Osteoclastoma

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2
Q

What are giant cell tumors comprised of?

A

Giant cells = osteoclasts

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3
Q

What age group is primarily affected by osteoclastomas?

A

20-40 years

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4
Q

Most giant cell tumors are (benign/malignant)

A

Benign (80%)

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5
Q

The term, ____ refers to giant cell tumors being born malignant, rather than undergoing malignant degeneration.

A

Quasimalignant

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6
Q

What is the typical pattern of destruction of a giant cell tumor?

A

Geographic lytic

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7
Q

What is the term for a tumor that extends into the epiphysis of a bone?

A

Subarticular extension
(Arise in metaphysis, extend into epiphysis)

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8
Q

How would a patient with a giant cell tumor present clinically?

A
  • age 20-40 yrs
  • localized pain & aching
  • joint pain (not reproducible) + decreased ROM
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9
Q

How would a giant cell tumor present differently from an enchondroma?

A

Painful
(Enchondroma generally asymptomatic)

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10
Q

What are the radiographic characteristics of a giant cell tumor?

A
  • geographic lytic lesion
  • narrow/short ZoT
  • IF expansile, bone surrounding lesion is very thin
  • frequently multiloculated
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11
Q

Which of the following is NOT a bone forming tumor?
A) enchondroma
B) osteoid osteoma
C) osteochondroma
D) osteoma

A

A

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12
Q

Which benign lesion is most likely to have pain?
A) osteoma
B) enostoma
C) osteoid osteoma
D) osteochondroma

A

C

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13
Q

Giant cell tumors spare ____ bone

A

subchondral (subarticular) bone

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14
Q

How can you tell the difference between a benign and malignant giant cell tumor?

A

appear the same, need a biopsy to tell

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15
Q

What are the imaging features of a giant cell tumor?

A
  • geographic lytic
  • multiloculated & septated
  • begins in metaphysis
  • subarticular extension
  • expansile
  • eccentric
  • absence of corticated border
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16
Q

What radiographic is characteristic of a giant cell tumor?

A

subarticular extension
(NOT pathognomonic)

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17
Q

What mnemonic is used for differential diagnoses of a non-aggressive lesion in the posterior elements of the spine?

A

Alphabet soup:
ABC / GCT / OB / OC / OO

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18
Q

An osteochondroma is also called ____

A

exostosis

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19
Q

What age group is primarily affected by osteochondroma?

A

skeletally immature (<20), but keep it for the rest of life

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20
Q

What is the most common benign skeletal tumor?

A

osteochondroma

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21
Q

What is the chance of malignant transformation of an osteochondroma?

A

<1%

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22
Q

What are the 2 types of osteochondroma?

A
  • pedunculated
  • sessile
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23
Q

What signs and symptoms would suggest malignant transformation of an osteochondroma? What follow-up would you suggest?

A

becomes painful w/ rapid growth
MRI or CT

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24
Q

What are the preferential locations of osteochondromas?

A

tubular bones + post. elements of spine (any endochondral ossified bones)
- femur
- humerus
- tibia
- pelvis
- ribs
- scapula

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25
Q

What is the name for the multiple form of osteochondroma?

A

Hereditary Multiple Exostosis (HME)

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26
Q

Hereditary Multiple Exostosis is also called ____

A

osteochondromatosis

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27
Q

What is the chance of malignant transformation of osteochondromatosis?

A

25%

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28
Q

What is a major difference between the solitary and multiple forms of osteochondroma in terms of possible outcomes?

A
  • solitary: <1% chance of malignant transformation
  • multiple: up to 25% undergo malignant transformation
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29
Q

If an osteochondroma undergoes malignant degeneration, what will it transform into?

A
  • chondrosarcoma (most likely)
  • osteosarcoma
30
Q

Describe the appearance of a pedunculated osteochondroma

A
  • thin, elongated bony stalk
  • cartilage cap (may be calcified)
  • should not be thicker than 10mm
  • metaphyseal
  • continuous cortex & medullary space
  • projects away from joint
  • lucent when en face
31
Q

Describe the appearance of a sessile osteochondroma

A
  • don’t often have cartilaginous cap
  • broad-based metaphysis
  • lucent when en face
32
Q

At what point is a pedunculated osteochondroma considered to undergo malignant transformation?

A

when cartilage cap >2cm thickness
(use MRI to evaluate)

33
Q

What is the preferential location of osteochondromas?

A
  • knee is common
  • pelvis, scapula, ribs
  • metaphysis near growth plate of endochondral bones only
34
Q

2 or more osteochondroma lesions is termed ____

A

Hereditary Multiple Exostosis (HME)

35
Q

How may a patient with a sessile osteochondroma present clinically?

A

Generally painless (non-tender), non-mobile, potentially palpable lump
Potential complications:
- tendinosis/bursitis
- neurovascular bundle compromise
- malignant transformation

36
Q

How would a patient with pedunculated osteochondroma present clinically?

A

Generally painless (non-tender), non-mobile, potentially palpable lumps
Potential complications:
- pathological fracture
- tendinosis/bursitis
- neurovascular bundle compromise
- malignant transformation

37
Q

How would a patient with Hereditary Multiple Exostosis present clinically?

A
  • begin forming both sessile & pedunculated osteochondromas 20-10 years old
  • commonly deformed metaphysis (Madelung-like deformity, dwarfism)
  • limited ROM
  • family Hx

(in addition to SSx of solitary osteochondroma)

38
Q

What is the term for the radiographic appearance of a sessile osteochondroma on the medial aspect of the femoral neck, commonly seen in patients with HME?

A

Brahma bull appearance

39
Q

What are your next steps for a patient with an osteochondroma with a cartilage cap that is 15mm in thickness?

A

MRI w/ contrast
(for 10-20mm thickness)

40
Q

What is a hemangioma?

A

slow-growing, solitary vascular neoplasm

41
Q

What are the 2 types of hemangiomas?

A
  • cavernous
  • capillary
42
Q

Where do cavernous hemangiomas occur?

A

spine
skull

43
Q

Where do capillary hemangiomas occur?

A
  • ribs
  • pelvis
  • metaphysis of long bones
44
Q

What is the most common benign bone tumor of the spine?

A

hemangioma

45
Q

What age group is primarily affected by hemangiomas?

46
Q

What is the clinical presentation of a hemangioma?

A
  • most are asymptomatic, incidental finding (not significant)
  • expansion can cause Sx of impingement & stenosis (rare)
47
Q

Where do hemangiomas most commonly occur?

A

75% in spine & skull
- lower thoracic & upper lumbar (TL)
- vertebral arch (10-15%)

48
Q

What radiographic sign is associated with hemangioma?

A

corduroy cloth/jail bar appearance
(vertically striated vertebra)

49
Q

At what point is corduroy cloth or jail bar appearance visible radiographically?

A

> 50% of vertebral body involved

50
Q

What causes corduroy cloth or jail bar appearance?

A

Wolf’s law: resorption of horizontal trabeculae, ^vertical trabeculae

51
Q

How does a hemangioma appear on MRI?

A

bright on both T1 and T2
(fat surrounds blood vessels)

52
Q

How does a hemangioma appear on CT?

A

polka dotted appearance

53
Q

How does a hemangioma in the skull appear radiographically?

A

geographic lytic lesion w/ matrix calcification:
- sand dollar
- sunburst or spoked-wheel

54
Q

What 2 conditions are on your list of differential diagnoses for a hemangioma?

A
  • paget Dz
  • osteoporosis
55
Q

How are soft tissue hemangiomas visualized radiographically?

A

round, well-formed phleboliths

56
Q

A 35 year old patient with a history of a single sessile osteochondroma arising from the medial aspect of the distal femur presents with pain immediately adjacent to that site. Light touch is intact, muscle testing of the leg is 5/5, and pulses are strong. What is the most likely explanation for why there is pain?
A) neurovascular bundle impingement
B) fracture
C) malignant degeneration
D) tendinosis/bursitis

57
Q

What DDx mnemonic is used for this lesion?

A

FEGNOMASHIC

58
Q

20 year old female with left wrist pain. Give 3 differentials in order from most to least likely.

A

(FEGNOMASHIC)
1. GCT (20-40, pain, subarticular sparing)
2. ABC (<20, pain, metaphyseal/epiphyseal)
3. Chondroblastoma (10-25, pain, epiphyseal)

59
Q

What is the diagnosis?

A

Hemangioma

60
Q

What sign is this?

A

Polka dot sign (hemangioma on CT)

61
Q

What imaging modality is this?

62
Q

What is the diagnosis? What bone is involved?

A

Sessile osteochondroma of medial fibula

63
Q

What is the diagnosis?

A

Sessile osteochondroma

64
Q

What is the diagnosis?

A

Hereditary Multiple Exostoses (HME)

65
Q

What is the diagnosis?

A

Pedunculated osteochondroma

66
Q

What is the likely diagnosis? What radiographic feature supports your diagnosis?

A

GCT - subarticular extension

67
Q

Give 4 reasons these may become painful.

A

(Osteochondromas)
- tendinosis/bursitis
- neurovascular bundle compromise
- malignant transformation
- fracture (Pedunculated only)

68
Q

What is the chance of malignant transformation?

A

(Osteochondromatosis/HME)
25%

69
Q

What is the name given to the radiographic appearance of the femoral necks?

A

Brahma bull appearance
(osteochondromatosis)

70
Q

What imaging finding indicates malignant degeneration of this condition? What would it degenerate to?

A

(Dx = Osteochondromatosis)
Cartilage cap thicker than 2cm
—> chondrosarcoma

71
Q

What is the diagnosis? What is the radiographic sign?

A

Hemangioma
Corduroy cloth (jail bar) sign

72
Q

What is the radiographic sign? What is the diagnosis?

A

Sand dollar appearance
Hemangioma