Professional Documents
Culture Documents
Hamartomas:
• Odontomas.
Malignant epithelial neoplasms:
• Odontogenic carcinomas.
Rare.
Benign mixed epithelial and connective tissue
neoplasm.
Neoplasm of both odontogenic epithelium
and mesenchyme.
Usually seen in children or young adult.
They are slow-growing and usually
asymptomatic, but expand the jaw.
Radiogragraphically these tumors resemble
ameloblastomas but develop in younger age
group.
Radiographical appearance of
ameloblastic fibroma
Site: mandible and rarely in maxilla (premolar-
molar region).
Shape: Multilocular
Monolocular in early stages
Outline :
Smooth, well defined and well corticated.
Radiolucent with internal radiopaque septa if
multilocular.
Effect
Adjacent teeth displaced
Rare.
These very similar non-invasive tumors originate from the
odontogenic connective tissue of the developing tooth germ
which produce either excessive collgen (fibroma) or excessive
ground substance(myxoma).
Usually seen in young adults.
Form a multilocular, (soap-bubble radiolucency). Occasionally
monolocular, smooth and often scalloped, well defined with
variable cortication.
Most common site is posterior mandible. Sometimes posterior
maxilla.
Effect = adjacent teeth displaced , extensive buccal and lingual
expansion.
Radiolucent non-odontogenic
tumors
Central haemangioma
Intrinsic primary malignant bone tumors
(osteosarcoma,fibrosarcoma and chondrosarcoma)
Extrinsic primary malignant tumors involving bone
(squamous cell carcinoma)
Secondary bone tumors
Lymphoreticular tumors of bone (multiple myeloma,
langerhans cell disease)
Giant cell lesions
Fibro-osseous lesions.
Central haemangioma
This is a rare, benign lesion that occasionally
affect the jaws, particularly mandible.
Developmental malformation of the blood
vessels in the marrow spaces, rather than a
true neoplasm.
Usually discovered in adolescents.
Life threatening nature of the lesion with a
very variable radiographic appearance,