Malignant Odontogenic tumours Flashcards

1
Q

Types of malignant odontogenic tumours?

A
  • Sclerosing odontogenic carcinoma
  • Ameloblastic carcinoma
  • Clear cell odontogenic carcinoma
  • Ghost cell odontogenic carcinoma
  • Primary intraosseous carcinoma, NOS
  • Odontogenic carcinosarcoma
  • Odontogenic sarcomas
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2
Q

Ameloblastoma carcinoma?

A
  • Rare, highly invasive and can metastasize.
  • Primary or arise by de- differentiation from
    conventional ameloblastoma.
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3
Q

Histopathology of ameloblastoma carcinoma?

A
  • Sheets and islands of basaloid cells with peripheral
    palisading.
  • Mitotic figures, nuclear and cellular pleomorphism,
    and necrosis.
  • Neural and vascular invasion.
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4
Q

Management of ameloblasts is carcinoma?

A
  • Similar to oral squamous cell carcinoma and
    involves surgical excision with clear margins.
  • Depending on the clinical stage of disease, a neck
    dissection may be required to remove the regional
    lymph nodes.
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5
Q

Primary intra-osseous squamous carcinoma?

A

Look like squamous cell carcinoma of the jaw

  • The majority of oral squamous cell carcinomas arise
    from surface mucosa but a small number arise from
    odontogenic epithelium in the jaws.
  • Some arise de novo and others in a pre- existing
    odontogenic cyst.
  • These neoplasms expand the jaws, show rapid
    growth, and may cause pathological fracture.
  • Histopathologically, they resemble conventional
    squamous cell carcinoma
    *Similar management
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6
Q

Clear cell odontgoenic carcinoma?

A
  • Rare, malignant with potential to metastasize.
  • Histopathologically, a biphasic pattern is often present with islands of epithelial cells possessing
    clear to faintly eosinophilic cytoplasm along with
    cords of dark- staining basaloid cells.
  • Management is similar to oral squamous cell carcinoma.
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7
Q

Ghost cell odontogenic carcinoma?

A
  • Very rare.
  • Behaviour is uncertain but some reported cases have metastasized.
  • Management is decided on a case by case basis but if worrying features are present, then treatment is planned as for oral squamous cell carcinoma
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8
Q

Odontogenic sarcomas?

A
  • Extremely rare.
  • Two variants:
  • Ameloblastic fibrosarcoma, the malignant counterpart of amleoblastic fibroma
  • Ameloblastic fibrodentinoma (ameloblastic fibroodontosarcoma), in which dental hard tissue
    formation may additionally be seen.
  • Both are treated by surgery with wide margins to ensure clearance.
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9
Q

Peduculated?

A

On a stalk

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10
Q

Congenital tumours of possible odontogenic origin?

A
  • Congenital epulis.
  • Melanotic neuroectodermal tumour
    of infancy.
  • Congenital odontogenic myxoma.
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11
Q

Clinical presentation of Congenital epulis?

A
  • Rare.
  • Newborn infants.
  • Incisor region of the maxilla.
  • The swelling is rounded and often pedunculated.
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12
Q

Histopathology of congenital epulis?

A
  • Large closely packed granular cells covered by oral
    mucosa.
  • Congenital gingival granular cell tumour.
  • Unlikely to be neoplastic and does not recur after
    excision.
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13
Q

Origin of Melanotic Neuroectodermal Tumour of Infancy?

A

Cells of neural crest

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14
Q

Clinical presentation of Melanotic Neuroectodermal Tumour of
Infancy?

A
  • Rare tumour in infants during the first year of life.
  • More frequent in the anterior maxilla.
  • Behaves aggressively and tends to recur.
  • Requires multiple attempts at excision.
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15
Q

Congenital odontogenic myxoma?

A
  • Rarely, odontogenic myxoma is present at birth.
  • The lesion expands the jaw and treatment is often delayed to allow some facial growth, with removal in early childhood.
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