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
2
Q
Ameloblastoma carcinoma?
A
- Rare, highly invasive and can metastasize.
- Primary or arise by de- differentiation from
conventional ameloblastoma.
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.
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.
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
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.
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
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.
9
Q
Peduculated?
A
On a stalk
10
Q
Congenital tumours of possible odontogenic origin?
A
- Congenital epulis.
- Melanotic neuroectodermal tumour
of infancy. - Congenital odontogenic myxoma.
11
Q
Clinical presentation of Congenital epulis?
A
- Rare.
- Newborn infants.
- Incisor region of the maxilla.
- The swelling is rounded and often pedunculated.
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.
13
Q
Origin of Melanotic Neuroectodermal Tumour of Infancy?
A
Cells of neural crest
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.
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.