Odontogenic Tumors Flashcards

1
Q

Odontogenic Tumors: 3 Tissue categories of origin

A
  1. Odontogenic Epithelium
  2. Mesenchymal
  3. Mixed
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2
Q

Tumors of Odontogenic Epithelium

A
  • Ameloblastoma
  • Adenomatoid odontogenic tumor
  • Calcifying epithelial odontogenic tumor
  • Squamous odontogenic tumor
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3
Q

Ameloblastoma types

A
  • Multicystic (solid conventional) – 86%
  • Unicystic – 13%
  • Peripheral – 1%
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4
Q

Ameloblastoma stats

A

• Usually 3rd to 7th decades, no gender predilection
• 85% mandible (molar/ramus most common), 15% maxilla
(usually posterior)

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5
Q

Ameloblastoma - Radiographic

A

• Multilocular radiolucency usually; soap bubble (large loculations),
honeycomb (small loculations)
• Buccal and lingual cortical expansion
• Often associated with an unerupted tooth (3rd molar)
• Margins may show irregular scalloping

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6
Q

Ameloblastoma and roots

A

Resorption of
adjacent tooth
roots is
common

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7
Q

Ameloblastoma – Treatment and Prognosis

A

• Enucleation and curettage (recurrence 50% to 90%)
• Marginal resection (recurrence up to 15%)
• En bloc resection, with at least 1 cm clear margins (highest cure rate)
• Radiation therapy not recommended, except to control nonresectable
tumors.

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8
Q

Desmoplastic Ameloblastoma

A

• The exception to the rules for conventional
ameloblastoma
– One of several histologic subtypes of ameloblastoma
– Preference for anterior jaws, most often maxilla
– Radiographically resembles a fibro-osseous lesion
– Mixed radiolucent/radiopaque appearance due to osseous
metaplasia within dense fibrous septa
– Varying opinions regarding aggressiveness of tumor and
recommended treatment

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9
Q

Unicystic Ameloblastoma

A

• 50% diagnosed during the second decade of life
• Over 90% are found in the mandible, usually posterior
• Circumscribed radiolucency, often surrounding the crown of an
unerupted third molar, similar to dentigerous cyst

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10
Q

Unicystic Ameloblastoma Dx guidlines

A

To be diagnosed as unicystic, the
ameloblastoma must be unicystic grossly,
radiographically, and histologically

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11
Q

Unicystic Ameloblastoma – Treatment and

Prognosis

A

• Enucleation is most common, although if the tumor is found to be
mural (satellites of ameloblastic epithelium within wall of cyst),
further treatment is indicated
• 10% to 20% recurrence after enucleation

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12
Q

Peripheral Ameloblastoma

A

• 1% of ameloblastomas
• GUM BUMP - Painless, non-ulcerated, sessile or pedunculated lesion
on gingiva or alveolar mucosa; usually posterior, more common in
mandible
• Average age 52
• Innocuous behavior. Local surgical excision recommended, with 15%
to 20% recurrence initially; second recurrence is rare.
• Rule out central ameloblastoma

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13
Q

Gum Bump Differential

A
Pyogenic granuloma
Fibroma
Ossifying fibroma
Peripheral giant cell
granuloma
Parulis
Others: Peripheral
odontogenic fibroma,
peripheral ameloblastoma
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14
Q

Malignant Ameloblastoma

A

• Less than 1% of all ameloblastomas
• Metastasis, with secondary tumors exhibiting histology similar to
primary tumor (benign cytology under the microscope)
• Mets to lungs most common… aspiration or implant mets. Metastasis
may also occur via blood or lymphatic channels
• Poor prognosis

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15
Q

Ameloblastic Carcinoma

A

• Cytologic features of malignancy either in primary or secondary
tumors (microscopically ugly)
• More aggressive, with ill-defined margins, destruction of cortex, and
extension into soft tissue
• Poor prognosis

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16
Q

Adenomatoid Odontogenic Tumor (AOT)

A

• 3%-7% of odontogenic tumors
• “Two thirds tumor”: Female, young (ages 10 to 19), anterior jaws,
maxillary, associated with impacted tooth, radiopacities
• Most often asymptomatic, less than 3 cm. May cause painless bony
expansion if large

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17
Q

Adenomatoid

Odontogenic Tumor

A
2/3’s tumor:
Female
Anterior
Maxillary
Young
Canine tooth
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18
Q

Adenomatoid Odontogenic Tumor – Radiographic

Features

A

• Unilocular radiolucency
• May contain fine calcifications – snowflake calcifications (mixed
RL/RO DDX)
• “Follicular” - associated with crown of unerupted tooth
• “Extrafollicular” – associated with or between tooth roots

19
Q

Adenomatoid Odontogenic Tumor – Treatment

and Prognosis

A
  • Enucleates very easily due to thick capsule
  • Recurrence after enucleation is rare
  • No reports of aggressiveness
20
Q

Calcifying Epithelial Odontogenic Tumor

CEOT, aka Pindborg Tumor

A
  • Less than 1% of odontogenic tumors, less than 200 reported cases
  • Wide age range, most common between 30 and 50 years
  • No gender predilection
  • Two thirds of cases reported in the mandible, usually posterior
  • Painless, slow growth
21
Q

Calcifying Epithelial Odontogenic Tumor

(CEOT) - Radiographic

A

• Radiolucent defect, most often multilocular
• Margins may be scalloped
• Frequent association with an impacted tooth, usually a mandibular
third molar
• Often contains calcifications that vary in density and size,
concentrated around crown of impacted tooth – amyloid material and
Leisegang calcifications

22
Q

Calcifying Epithelial Odontogenic Tumor –

Treatment and Prognosis

A
  • Conservative resection, including a narrow rim of surrounding bone
  • Posterior maxillary lesions may require more aggressive treatment
  • Recurrence rate 15%
  • Good prognosis
23
Q

Tumors of Odontogenic

Ectomesenchyme

A
  • Odontogenic Fibroma (central)
  • Granular Cell Odontogenic Tumor
  • Odontogenic Myxoma
  • Cementoblastoma
24
Q

Odontogenic Fibroma

A

• Histology may look the same as a hyperplastic dental
follicle – correlation with clinical and radiographic
presentations necessary

25
Q

Odontogenic fibroma locations

A

• 45% maxillary, mostly anterior to the first premolar
• 55% mandible, half of which are posterior to the first
molar

26
Q

Odontogenic fibroma gender predilection and avg age

A
  • Wide age range, mean age 40 years

* F>M, app 2:1

27
Q

Clinical and radiographic presentation of Odontogenic Fibroma

A

• Clinical notch or depression in the palate is characteristic of maxillary
OF’s
• Small lesions appear unilocular; large lesions can appear multilocular
• 12% exhibit radiopaque flecks
• Root resorption is common; also root divergence
• Two accepted histologic presentations: simple type and WHO type

28
Q

Odontogenic fibroma tx and prognosis

A
  • Enucleation and vigorous curettage

* Recurrences uncommon, prognosis good

29
Q

Odontogenic Myxoma age, location and gender facts

A

• Commonly young adults, average age 25-30 years, no
gender predilection
• Any location within jaws, mandible more common

30
Q

Odontogenic Myxoma Radiographic appearance

A

• Radiographic: Uni- or multilocular radiolucency,
irregular or scalloped margins
• Thin trabeculae of bone arranged at right angles
• May exhibit a soap bubble pattern

31
Q

Odontogenic Myxoma – Treatment and Prognosis

A

• Small lesions may be treated with curettage, but follow-up is
necessary
• Larger lesions may need resection due to infiltration of surrounding
bone
• Recurrence near 25%
• Overall good prognosis, no reported metastases
• Rare myxosarcoma: cellular atypia and more aggressive; No
metastasis

32
Q

Cementoblastoma

A
• Age: Young adults; <25
yrs
• Sex: No predilection (M?)
• Site: 75% in mandible, 1st
molar
• Radiographic:
Pathognomonic –
attached to a tooth root
• Clinical: May be painful
and expansile
• Completely excise
33
Q

Mixed Odontogenic Tumors

A
  • Composed of ectomesenchymal and odontogenic epithelial elements
  • Compound and complex odontomas
  • Ameloblastic fibroma
  • Ameloblastic fibro-odontoma
  • Ameloblastic fibrosarcoma
34
Q

Odontoma

A

Hamartoma (developmental anomaly)
• Compound – multiple small structures resembling teeth; most common
• Complex – conglomeration of enamel and dentin
• Mean age is 14 years
• More common in the maxilla
• Usually asymptomatic, associated with failure of tooth eruption

35
Q

Odontoma Radiographic presentation

A

Radiographically exhibits radiodensity similar to teeth,

surrounded by a narrow radiolucent rim

36
Q

Odontoma Tx

A

Local excision, excellent prognosis

37
Q

Ameloblastic Fibroma

A

• Both the epithelial and mesenchymal tissues are neoplastic
• Most often diagnosed within first two decades of life; males slightly
outnumber females
• 70% posterior mandible; may grow large
• Radiographically, unilocular or multilocular radiolucency, welldefined,
possibly sclerotic border
• 75% associated with unerupted tooth

38
Q

Ameloblastic Fibroma – Treatment and Prognosis

A

• Initial lesions are treated conservatively, with local excision or
curettage
• Recurrent lesions are treated with more aggressive surgical resection
• Recurrence rates reported from 0 to 45% after conservative removal

39
Q

Ameloblastic Fibro-Odontoma

A

• Similar to ameloblastic fibroma, but contains enamel and dentin
• Average age of diagnosis is 10 years (younger than ameloblastic
fibroma)

40
Q

Ameloblastic Fibro-Odontoma Radiographically

A

Radiographically contains variable amounts of calcified material as small
radiopacities or large comglomerations; often associated with an unerupted
tooth

41
Q

Ameloblastic fibro odontoma

A

Treatment consists of conservative curettage, shells out easily;
recurrence is rare, prognosis is excellent

42
Q

Ameloblastic Fibrosarcoma

A

• Malignant counterpart of ameloblastic fibroma
• Mesenchymal tissue is malignant
• 45% of cases arise from a recurrence of ameloblastic fibroma or
ameloblastic fibro-odontoma
• 1.5 times as common in males, average age 27 years
• 80% occur in the mandible, exhibiting pain, swelling, and rapid
growth

43
Q

Ameloblastic Fibrosarcoma

Radiographically

A

ill-defined radiolucency, destructive

44
Q

Ameloblastic Fibrosarcoma

Treatment

A
Radical surgery is
recommended
• Death usually occurs
due to uncontrolled,
aggressive local disease