Exam 1 - Mixed Flashcards

1
Q

What does a cementoblastoma arise from?

A

PDL of the tooth

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2
Q

Name that lesion: Opaque mass fused to roots, thin lucent rim around mass in mature lesions

A

Cementoblastoma

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3
Q

What it the tx of cementoblastoma?

A

It is a benign tumor so it needs to be removed. Conservation excision with either root amputation, endo, or ext.

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4
Q

What is the recurrence rate for a cementoblastoma after tx?

A

LOW

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5
Q

What would you see when looking at a cementoblastoma under a microscope?

A

Cellular cementum with plump cementoblast, often a periphery of radiating columns of calcified material

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6
Q

What may a cementoblastoma be mistaken for under a microscope?

A

Osteosarcoma

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7
Q

What is key in diagnosing a cementoblastoma?

A

Correletating history, radiograph, and histology

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8
Q

What is the most common odontogenic tumor?

A

Odontoma

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9
Q

Name the lesion:

Benign odontogenic tumor that contains odontogenic tissues but does not form small tooth appearing structures

A

Complex odontoma

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10
Q

What is the common location to find complex odontoma?

A

Complex- Posterior jaw; frequently pericoronal to an impacted tooth

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11
Q

Describe odontoma histology.

A

Show tooth like forming structures (dentin, enamel, pulp) but shows them in abnormal fashion

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12
Q

What is the common location to find compound odontoma?

A

Compound - Anterior jaws; may be associated with unerupted tooth
Resembles small teeth (toothlets/denticles)

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13
Q

T/F Tx of odontoma with enucleation you will likely see recurrence.

A

False NO recurrence

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14
Q

______ _______ __________(COC)/ Gorlin Cyst
is usually a unilocular RL, but up to ___ can have calcifications (mixed appearance).
May be associated with _______ tooth.

A

Calcifying odontogenic cyst (COC)/ Gorlin cyst is usually a unilocular RL, but up to 50% can have calcification (mixed appearance)
May be associated with unerupted tooth.

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15
Q

What region are you most likely to find a Gorlin cyst/ COC?

A

Anterior portion of the jaw 65%

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16
Q

What is the recurrence of gorlin cyst with enucleation?

A

unlikely recurrence

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17
Q

3 tumors that come from odontogenic epithelium

A
  1. Ameloblastoma
  2. Adenomatoid odontogenic tumor
  3. Cacifying, epithelial odontogenic tumor
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18
Q

3 tumors that come from odontogenic ectomesenchyme

A
  1. Odontogenic fibroma
  2. Odontogenic myxoma
  3. Cementoblastoma
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19
Q

3 tumors that come from odontogenic epithelium and ectomesenchyme (mixed)

A
  1. Ameloblastic fibroma
  2. Ameloblastic fibro odontoma
  3. Compound or complex odontoma
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20
Q

Name that lesion: Looks virtually identical to a complex odontoma

A

Ameloblastic fibro-odontoma

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21
Q

Where is Ameloblastic fibro-odontoma most commonly located?

A

posterior mandible

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22
Q

What age range is most common to find Ameloblastic fibro-odontoma?

A

average age 10 yrs old

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23
Q

Name that lesion:

Mixed lesion, <20 yrs, with 80% being in anterior jaw; unilocular RL which may develop snowflake/ fleck-like radiopacities

A

Adenomatoid odontogenic tumor (AOT)

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24
Q

Adenomatoid odontogenic tumor (AOT) ____ with unerupted teeth (most often canine) where RL extends beyond ___.

A

Adenomatoid odontogenic tumor (AOT) 75% with unerupted teeth (most often canine) where RL extends beyond CEJ.

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25
Q

Name that lesion: Has snowflake/fleck like RO, tx enucleation

A

Adenomatoid odontogenic tumor (AOT)

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26
Q

Calcifying epithelial odontogenic tumor (CEOT) is most likely to be found where and what age group?

A

In posterior jaw often with an impacted tooth and >30 yrs

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27
Q

Fall under category of benign odontogenic cyst/tumor with calcifications (4 things he talked about)

A

Calcifying Odontogenic Cyst (COC) - AKA Gorlin Cyst

Ameloblastic fibro-odontoma

Adenomatoid odontogenic tumor (AOT)

Calcifying epithelial odontogenic tumor (CEOT)

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28
Q

How do you treat a calcifying epithelial odontogenic tumor (CEOT)?

A

Conservative resection

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29
Q

T/F: All of the benign odontogenic cyst and tumors are asymptomatic or present with slow growing swelling/expansion.

A

True

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30
Q

What is another name for paget disease of bone?

A

Osteitis deformans

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31
Q

Name the lesion: Pathogenesis is Increased uncontrolled bone remodeling resulting in thickened but distorted and weakened bones

A

Paget disease

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32
Q

Paget Disease:
Unknown etiology

> ____ yrs

_______ _______ ancestry

May have bone pain and possible _______

A

Paget Disease:
Unknown etiology
> 40 yrs
Anglo-saxon ancestry
May have bone pain and possible fractures

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33
Q

Paget Disease:

Most cases are ________ (85%) affecting pelvis, femur, ______ vertebrae, _____ (hat doesnt fit) and _______ most common

A

Most cases are polyostotic (85%) affecting pelvis, femur, lumbar vertebrae, skull (hat doesn’t fit) and tibia most common

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34
Q

Paget disease is more likely to affect the mandible or maxilla?

A

Maxilla causes symmetric enlargement (denture doesn’t fit) space develops between teeth

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35
Q

T/F Enlargement of bones in paget disease has the potential to pinch nerves leaving pt deaf and blind. (Narrowing ostea)

A

True

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36
Q

What is the marker of osteoblastic activity in paget disease?

A

Elevated total serum alkaline phosphatase

37
Q

Paget Disease: Chronic progression from _________ (lytic) phase to late lesions that show patchy ______ (“cotton-wool”) appearance with thickened ______. This is the classic cotton-wool appearance!

A

Chronic progression from vascular (lytic) phase to late lesions that show patchy sclerosis (“cotton-wool”) appearance with thickened cortices. This is the classic cotton-wool appearance!

38
Q

What may you see in teeth of pt with paget disease?

A

Extensive hypercementosis of teeth

39
Q

How do you tx paget’s disease?

A

NSAIDS for mild pain

Bisphosphanates - help slow bone turnover

40
Q

What do you need to monitor pt for with pagets disease?

A

They can develop bone tumors (ex. osteosarcoma)

41
Q

What are dental considerations with paget disease?

A

Difficult ext due to hypercementosis and ankylosis
Place implants with caution
Surgical Bleeding risk during vascular lytic phase
Poor wound healing with risk for osteomyelitis during sclerotic phase

42
Q

Fibro-osseous lesion:
Non specific term that describes a group of process with different pathogenesis, where normal bone is replaced by ______ tissue with a newly formed ___________ product.

A

Non specific term that describes a group of process with different pathogenesis, where normal bone is replaced by fibrous tissue with a newly formed mineralized product.

43
Q

What does an accurate diagnosis of fibro-osseous lesions require?

A

Accurate diagnosis requires correlation of the clinical and radiographic features with the microscopic features because they look very similar microscopically ***

44
Q

What are the three fibro-osseous lesions?

A
  1. Fibrous Dysplasia
  2. Ossifying fibroma (central) (COF)
  3. Cemento-osseous dysplasia (Focal, PA, and Florida variants)
45
Q

When do you often discover fibrous dysplasia?

A

Early 20s, 2nd to 3rd decade

46
Q

Fibrous dysplasia is a developmental, tumor like lesion due to a mutation in the _________ ___ protein gene (ie. GNAS)

A

Fibrous dysplasia is a developmental, tumor like lesion due to a mutation in the stimulatory G protein gene (ie. GNAS)

47
Q

Fibrous dysplasia is usually monostotic (one bone only); in which ______ are commonly affected.
When _________ (more than one bone) you may see see ______ ___ _____ pigmentation and _______ problems.

A

Fibrous dysplasia is usually monostotic (one bone only); in which jaws are commonly affected.
When polyostotic (more than one bone) you may see see cafe au lait pigmentation and endocrine problems.

48
Q

Fibrous dysplasia in the maxilla may involve adjacent facial bone causing facial deformity calle ______ _______ ________.

A

Craniofacial fibrous dysplasia

49
Q

What is the appearance usually if you catch fibrous dysplasia early?

A

RL or mottled followed by classic “ground glass” (really close trabeculae with fibrous stuff loose in between) pattern with blending margins so no RL rim or capsule

(why? Abnormal bone fuses to adjacent normal bone - no capsule)

50
Q

How do you treat fibrous dysplasia?

A

Wait till the person is done growing. At that point you decide definitive tx that should be done for it.

Conservative management advised

Surgical reduction on if significant cosmetic or functional deformity (up to 50% can show regrowth)

51
Q

What percent can show regrowth in fibrous dysplasia?

52
Q

T/F Fibrous dysplasia is not a true neoplasm it or a tumor so you better not do a resection on the pt.

53
Q

What type of border will you see in fibrous dysplasia?

A

Blending border

54
Q

Name that lesion: Benign neoplasm considered by most to be derived from bone, though often also has cementum like material in it. Asymptomatic when small, and painless swelling when large.

A

Central Ossifying Fibroma (COF)

55
Q

Name that lesion:

Starts off RL then develops some calcifications. Keeps RL periphery. Histology usually shows smooth surgical margin, with fibrous and osseous tissue and cementum sphericules

A

Central Ossifying Fibroma (COF)

56
Q

Central Ossifying Fibroma (COF) location

A

mandible far more than maxilla especially posterior region

57
Q

Demographic and age for a pt with Cemento-osseous dysplasia (COD)

A

Middle age >30 yrs females, mostly in african americans

58
Q

What fibro-osseous lesion does this match Central ossifying Fibroma or Cemento-osseous dysplasia: Painless, typically NO expansion, around tooth roots/apices and teeth are vital. Well defined but irregular borders. RL at first and will slowly develop central RO.

A

Cemento-osseous dysplasia (COD)

COF is well defined, unilocular, expansile.

59
Q

Describe cemento-osseous dysplasia lesion tissue appearance.

A

Lesional tissue appears as really fragmented, gritty (like little coffee grounds), red/brown tissue (different than COF or FD) early on and denser as it matures

60
Q

What is important when diagnosing early cemento-osseous dysplasia lesions.

A

Doing a tooth vitality test so you don’t do RCT thinking its a PA cyst/granuloma.

61
Q

T/F: Cemento-osseous dysplasia is not a tumor and will not continue to grow the way fibrous dysplasia grows.

62
Q

How do you treat Cemento-osseous dysplasia?

A

None just radiographic follow up

63
Q

T/F Cemento-osseous dysplasia can appear in multiple different lesions in the jaw.

64
Q

Name the variant of Cemento-osseous dysplasia: posterior mandible, solitary lesions, may mimic COF requiring biopsy

65
Q

Name the variant of Cemento-osseous dysplasia: anterior mandible predominantly, often with multiple lesions

A

Periapical

66
Q

Name the variant of Cemento-osseous dysplasia: bilateral mandible (ant & post); can affect all 4 quadrants (Mx & Md); dense RO that can fuse to roots, possible expansion

67
Q

T/F Florid Cemento-osseous dysplasia dense RO that can fuse to roots.

68
Q

With _______ Cemento-osseous dysplasia if there is dense bone exposure it can cause 2ndary infection and sequestration. So be sure to avoid EXT and losing bone b/c don’t want it to be exposed and become infected (osteomyelitis)

69
Q

T/F Florid Cemento-osseous dysplasia can expand the bone while the other ones don’t.

A

False florid does but also central ossifying fibroma does

70
Q

What is the age that cementoblastoma often occurs?

A

Young adults

71
Q

Osteoblastoma:
2-4 cm up to 10 cm
Dull Pain and expansion are common
Well/ill-defined RL with patchy to diffuse mineralization

72
Q

What is histologically identical to a cementoblastoma but NOT fused to a tooth root?

A

Osteoblastoma

73
Q

Age you are most likely to find Cementoblastoma

A

Young Adults

74
Q

Age you are most likely to find Odontoma

A

Detected before 20 usually

75
Q

Age you are most likely to find Calcifying odontogenic cyst (COC) / Gorlin Cyst

A

Wide age range

76
Q

Age you are most likely to find Ameloblastic fibro-odontoma

A

average age is 10 yrs old

77
Q

Age and demographic you are most likely to find Paget disease

A

> 40 yrs anglo saxon ancestry

78
Q

Age you are most likely to find Fibrous dysplasia

A

2nd to 3rd decade usually adolescent early 20

79
Q

Age and demographic you are most likely to find Cemento-osseous dysplasia (COD)?

A

Middle age >30 yrs females, mostly in african americans

80
Q

Region most likely to find cementoblastoma

A

posterior mandible, especially 1st permanent molar

81
Q

Region most likely to find Odontoma (compound and complex)

A

associated with unerupted tooth and prevent closing gaps

Compound - anterior jaws maybe with unerupted teeth (toothlets)
Complex- posterior jaw pericoronal to an impacted teeth (does not form small tooth appearing structures.

82
Q

Region most likely to find Calcifying Odontogenic Cyst (COC) - AKA Gorlin Cyst

A

Anterior jaw 65% of the time

83
Q

Region most likely to find Ameloblastic fibro-odontoma

A

posterior mandible

84
Q

Region most likely to find Paget disease

A

Maxilla > mandible

85
Q

Region most likely to find Fibrous dysplasia

A

Usually monostotic (one bone only); jaws are commonly affected

86
Q

Region most likely to find Central Ossifying Fibroma (COF)

A

mandible > maxilla, posterior region most common

87
Q

Age most likely to find Osteoblastoma

A

Most pt are <30 yrs

88
Q

What three mixed lesions did we talk about that are associated with pain?

A

Cementoblastoma
Paget Disease
Osteoblastoma (dull pain)

89
Q

________ __________ is a developmental, tumor like lesion due to a mutation in the stimulatory G protein gene (ie. GNAS)

A

Fibrous dysplasia