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SINUS
SQUAMOUS CELL CARCINOMA ORIGINATING IN A CYST
CENTRAL MUCOEPIDERMAIOD CARCINOMA
MALIGNANT AMELOBLASTOMA AND AMELOBLASTIC
CARCINOMA
METASTATIC TUMORS
OSTEOSACOMA
Disease Mech.:
Uncommon and exclude invasions
May arise from inflammatory periapical,
residual, dentigerous and OKC.
Squamous epithelium lining gives rise to
malignant neoplasm
Clinical features:
Pain ( dull/long duration ) , Swelling , Pathologic
fracture fistula formation and regional
lymphadenopathy, sinus pain and swelling
Disease mech.:
Rick factors: chronic sinusitis,
chemicals(volatile hydrocarbons , isopropyl
oils, wood dust), metals(Ni , Cr)
Clinical features:
commonly(Africans/Asia heritage)
M>F
Initial sings=to inflammatory disease and may
include recurrent sinusitis, sinus pain , nasal
obstruction, epistaxis
CENTRAL MUCOEPIDERMAIOD
CARCINOMA
Disease Mech.:
epithelial tumor arising in bone originate
from(pluripotential odontogenic epithelium , or a
cyst lining)
Presence of intact cortical plates, radiographic
evidence of bone destruction
Clinical features:
F>M
Mimic a benign tumor or cyst
Painless swelling / facial asymmetry / tenderness /
parasthesia of ID / spreading to regional lymph
nodes
Internal structure:
Often multilocular / soap bubble /
honeycomb
Round radiolucent area
with/without thick sclerotic bony
peripheries
Effect on surrounding
structures:
Expansion of adjacent
cortical plates
Expansion into the
surrounding soft tissue
Mand canal may
depressed/ push
laterally-medially
Adjacent lamina dura
may lost / unaffected
teeth
D/D:
Recurrent ameloblastoma = peripheries and
internal structures
Odontogenic myxoma
CGCG
Management :
Treated surgically with resection encompassing
a margin of adjacent normal bone
Postoperative radiation therapy ( to control
spread to lymph nodes )
METASTATIC TUMORS
Disease Mech.:
Usually by blood vessels
Metastatic lesions in jaws usually arise from sites inf
to clavicle
>1%
Clinical features:
(2)f>M
Common in 5th-7th decade
Dental pain/ numbness/ parasthesia of 3 rd branch of
trigemenal nerve / pathologic fracture / hemorrhage
Imaging features:
Location:
1st common: post. area / mand>max
2nd common: max sinus . Followed by ant hard palat
and mand condyle
Frequently Bilateral in mand
May locate in periodontal ligament space / papilla of
developing tooth
Periphery and shape:
Moderately well demarcated / no cortication or
encapsulation / may have ill defined invasive
margins
Polymorphous in shape
Metastatic
breast
carcinoma . It
has destroy Inf.
.border of mand
Bilateral
metastatic
lesions from
the lung
destroying the
mand. ramus
Metastatic
thyroid
lesion
destroying
left condyle
Invasion
into
surrounding
soft tissue
Internal structures:
Generally radiolucent
Sclerotic metastases (prostate/breast)
Effect on surrounding structures:
Stimulate periosteal reaction
(prostate/neuroblastoma)
Effect lamina dura / increase width of
PDL space
Loss of bone support
Cortical bone of adjacent structures
destroyed
Resorption of teeth rare
Prostate
metastatic
causing
sclerosis
and
periosteal
reaction
Widening
in
periodont
al space
D/D:
Multiple myeloma
Periapical inflammatory lesion
Odontogenic cyst
SCC
Management:
Poor prognosis
Usually dies within 1-2 yrs
Chemotherapy , radiotherapy , surgery ,
immunotherapy , hormone therapy
OSTEOSACOMA
Disease Mech.:
Unknown cause (genetic/ viral cause
have been suggested)
Associated with paget dis , fibrous
dyplasia after radiotherapy
Osteoid is produced directly by
malignant stroma
Three major histologic types:
Chondroblastic , osteoblastic ,
fibroblastic
Clinical features:
Rare ( 7% of all osteosarcoma )
(2)M>F
4th decade
Rapid swelling / pain / tenderness / loose teeth/
erythema
May involve neurovascular canals
Location :
mand>max(commonly post areas , lesion occur in
any part)
May cross the midline
Internal structure :
radiolucent/ mixed/ radiopaque
Granular/ sclerotic appearing , cotton balls ,
honeycomb
D/D:
Minimal/absent of abnormal bone
(fibrasarcoma/ metastatic carcinoma)
Osseous structure is visible
( chondrosarcoma )
New bone presence ( prostate/ breast
metastases )
Ewing sarcoma , osteomyelitis , solitary
plasmacytoma
Management:
- Resection with large border
-radio/chemotherapy