Odontogenic tumours and tumour-like malfunctions Flashcards

1
Q

Classification system for odontogenic tumours and tumour-like malfunctions

A

Benign
- Od epithelium without Od ectomesenchyme (ameloblastoma and CEOT)
- Od epithelium with Od ectomesenchyme with hard tissue
- mesenchyme and od ectomes (fibromyxoma and cementoblastoma)

Malignant
- Od carcinomas (malignant ameloblastoma and ameloblastic carcinoma)
- Odontogenic sarcomas (ameloblastic fibrosarcoma)
- Od carcinosarcoma

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2
Q

Ameloblastoma

A

Rare, non cancerous tumour that develops most often int the jaw near the molars.

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3
Q

Odontoma

A

Tumour, benign
Require surgical removal
made up of dental hard tissue that resembles abnormal teeth or calcified mass that invade around your teeth and could affect how your teeth develop

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4
Q

aetiology ameloblastoma

A

injury to mouth/jaw, infections of the teeth/gums
infections by viruses or lack of protein or minerals

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5
Q

development of ameloblastoma

A

arises of Od epithelium
epithelium has marked proliferative capacity
grows by epithelial proliferation, extends between trabeculae of bone

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6
Q

Ameloblastic fibroma

A

rare
younger pts
uni/multilocular

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7
Q

Epidemiology ameloblastoma

A

commonest odontogenic tumour
rare under 10yrs
peak around 30-60 yrs
M=F
80% near in mandible near angle

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8
Q

clinical presentation ameloblastoma

A

not site specific
incidental finding

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9
Q

radiological features ameloblastoma

A

large
radiolucent
multilocular
expand bone, displace and resorb bone teeth
often destroys lower border of mandible

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10
Q

histological feature ameloblastoma

A

ameloblastoma
- strands and islands of epithelial cells
- tall columnar cells at periphery
- loosely packed smaller central cells resembling stellate reticulum

ameloblastic fibroma
- solid tumour
- predominately mesenchymal, ameloblasta-like epithelium as less component
- no calcification of matrix
- hard tissue is present

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11
Q

management of ameloblastoma

A

requires resection at least 15mm beyond radiological margins
recurrence inevitable if removal incomplete
annual follow up 5yrs then 3yrs thereafter
benign but up to 5% registered as death due to tumour
malignant transformation rate

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12
Q

Aetiology of odontome

A

local trauma
infammatory
infectious processes
hereditary anomalies such as Gardener’s Syndrome and Hermanns Syndrome
odontoblastic hyperactivity
mature odontoblasts
dental lamina remnants (cell rests of serres)

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13
Q

development of odontome

A

bulk formed by dentine
areas of active odontogenesis, reduced enamel epithelium and pulp may be present

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14
Q

CEOT

A

Calcifying epithelial odontogenic tumour
rare
older patients
pre-molar, molar region
multilocular

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15
Q

AOT

A

Adenomatoid Odontogenic Tumour (AOT)
rare
younger pts
maxilla
anterior to molar region
unilocular
speckled calcification
associated with U/E tooth

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16
Q

CCOT

A

Calcifying cystic odontogenic tumour
rare
younger pts
either jaw
anterior to molar region
unilocular
large
varying calcification
associated with U/E tooth

17
Q

CB

A

Benign cementoblastoma
young females predominately 15-30yrs
well defined speckled radiopaque mass attached to root mandibular molar or premolar tooth
peripheral radiolucent zone
resorption of tooth root

18
Q

CF

A

Cemento-ossifying fibroma
young adults
F>M
Well defined radiolucent mass in mandible near roots of teeth
cellular fibrous tissue with calcified bone/cementum
benign tumour

19
Q

Epidemiology odontome

A

70% tumours
young patients
F>M
Maxilla>Mandible
Gardener’s syndrome

20
Q

Radiological features of odontomes

A

speckled/dense radiopacity with radiolucent areas
circumscribed mass, well-defined periphery
may displace adjacent teeth

21
Q

histological CEOT

A

sheets and islands of pleomorphic and hyperchromatic epithelium
amyloid accumulation with epithelial groups
calcification of amyloid material

22
Q

histological AOT

A

tubular structures of ameloblast-like epithelium
sheets of cuboidal/spindle epithelial cells
calcification of intratubular secretions

23
Q

histological CCOT

A

Ameloblastic like epi
calcification of ghost cells
irregular dentine may be produced

24
Q

histological CB

A

mass of cementum resembling pagetic bone
pleomorphic cementoblasts
unmineralised osteo-cementum at border

25
Q

management of odontomes

A

enucleation
gardener’s syndrome
- multiple odontomas
- supernumerary
- shortened/deformed roots