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Benigntumorsofjaw2 130421054527 Phpapp01
Benigntumorsofjaw2 130421054527 Phpapp01
MODERATED BY:
jaw
DR. SUNITA GUPTA
DR. SHALINI
DR. DEEPMALA
DR. VIPUL
DR. ANSHUM
By:
VARUN
SURYA
1
Features
Benign tumor
Malignant tumor
Periphery
Smooth, well
defined,
Encapsulated,
corticated
Surrounding tissue
Compressed
Invaded
Size
Usually small
Often larger
Growth rate
Slow
Rapid
Spread
Direct extension
Metastasis
Location
Specific anatomic
site
Anywhere
Internal structure
RO , RL , mixed
Radiolucent
Destroy supporting
alveolar bone so that
teeth may appear
floating in space
Benign
Clinical Features
Radiologic features
LOCATION
Many tumors have a specific anatomic
predilection
odontogenic occur in the alveolar
lesions
processes
Above the inferior alveolar
nerve canal, where tooth
formation occurs
Vascular and
may originate inside the
neural lesions mandibular canal, arising
from the Neurovascular
tissues
Cartilaginous
tumors
INTERNAL STRUCTURE
It may be completely radiolucent or
radiopaque or maybe a mixture of
radiolucent and radiopaque tissues.
If the lesion contains radiopaque
elements, these structures usually
represent either residual bone or a
calcified material that is being
produced by the tumor.
For instance curved septa that are
characteristic in ameloblastoma represent
residual bone trapped inside the tumor
that has remodeled into curved septa.
The ameloblastoma does not produce
bone.
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.
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Benign tumors
The benign neoplasias are separated into
two major
groups: odontogenic tumors and nonodontogenic
tumors.
ODONTOGENIC
TUMORS
Odontogenic tumors arise from the tissues of
the odontogenic apparatus
According to (WHO),
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(i). Ameloblastoma
(ii). Squamous odontogenic tumor
(iii).Calcifying epithelial
odontogenic tumor (Pindborgs tumor)
(iv).Clear cell odontogenic tumor
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Odontogenic
epithelial
tumors
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AMELOBLASTOMA
Synonyms
Adamantinoma , adamantoblastoma, and
epithelial odontoma
Definition
A true neoplasm of enamel organ type which
doesnt undergo differentiation to the point of
enamel formation.
robinson Defined it as
A tumor that is -Unicentric,
non functional,
intermittent in growth,
anatomically benign
and clinically persistent
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Clinical features
Age - 20 to 40yrs
Site - mandible > maxilla
slow growing, painless, bony expansion
initially Tennis ball like consistency
Egg shell like cracking
Jaw bone enlargement & parasthesia
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Radiographic Features
Location. Most (80%) develop in the
molar-ramus region of the mandible, but
they may
extend to the symphyseal area.
Periphery. is usually well defined
and frequently delineated by a cortical
border. The
border is often curved and in small lesions
the border
and shape may be indistinguishable from a
cyst
The periphery of lesions in the maxilla is
usuallymore ill defined.
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internal compartments.
These septa are usually coarse and curved
and
originate from normal bone that has been
trapped
within the tumor.
Because this tumor frequently has internal
cystic components, these septa are often
remodeled into curved shapes providing a
honeycomb (numerous small compartments
or loculations) or soap bubble (larger
compartments of variable size)patterns .
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Egg shell
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Differential Diagnosis
The odontogenic keratocyst may contain
curved septa but usually the keratocyst
tends to grow along the bone without
marked expansion, which is Characteristic of
ameloblastomas.
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Treatment
The most common treatment is surgical
resection. If
the ameloblastoma is relatively small , it may
be removed
completely by an intraoral approach and
larger lesions
May require resection of the jaw.
The maxilla is usually treated more
aggressively because of the tendency of
ameloblastoma to invade adjacent vital
structures.
Radiation therapy may be used for inoperable
tumors,
Especially those in the posterior maxilla.
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Clinical features
CEOT
Central
(intraosseous)
age - 40yrs
site - 2/3rd of
lesions in mandible
slow growing.
painless mass.
Peripheral
(extraosseous)
site - anterior gingiva
appears as superficial
soft tissue swelling
of gingiva in a tooth
bearing area or
edentulous area
of jaw
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Radiographic features:
Location. mandible
most develop in the premolar-molar
area, with a
52% association with an unerupted or
impacted tooth.
Periphery. The border may have a welldefined cyst like
cortex. In some tumors the boundary maybe
irregular
and ill defined
Internal structure. The internal aspect
may appear unilocular or multilocular with
numerous scattered,
radiopaque foci of varying size and
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Treatment
The treatment of the CEOT is more
conservative than
the ameloblastoma , with local resection
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MIXED TUMORS
(OF ODONTOGENIC
EPITHELIUM
AND
ODONTOGENIC
ECTOMESENCHYME)
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ODONTOMA
Most common type of odontogenic tumor
Definition:
a tumor that is radiographically and histologically
characterized by the production of mature
enamel, dentin, cementum,and pulp tissue.
Clinical features:
Age- 10 to 20yrs
Site - Maxilla > mandible
Slow growing , hard , painless mass
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Features
Compound
complex
location
anterior maxilla in
association with the
crown of an
unerupted canine.
mandibular first
and second molar
area.
Internal
irregular mass of
calcified tissue
Frequency
More
Less common
Sex predilection
M=F
More in female
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Radiographic Features
Location.
compound odontomas (62%) occur in the
anterior maxilla in association with the crown
of an unerupted canine.
70%of complex odontomas are found in the
mandibular first and second molar area.
Complex odontoma
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Compound odontoma
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treatment
Complex and compound odontomas are
usually
Removed by simple excision. They do not
recur and are
not locally invasive
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AMELOBLASTIC FIBROMA
Synonyms
Soft odontoma, soft mixed odontoma, mixed
odonto genic tumor,
fibroadamantoblastoma,and granular cell
Ameloblasticfibroma
defination
Ameloblastic fibromas are benign, mixed
odontogenic
tumors. They are characterized by neoplastic
proliferation of maturing and early functional
ameloblasts,as
well as the primitive mesenchymal
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components of the
Clinical features:
Age- 5 to 20yrs
Site - Maxilla > mandible
Sex- no sex predilection
They usually produce a painless,slow-growing
expansion, and displacement of the involved
teeth
Radiographic
Features
Location. in the premolar-molar area of the
mandible
Periphery. The borders of an ameloblasticfibroma are
well defined and often corticated in a
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Differential Diagnosis
Ameloblastomahowever ,the ameloblastic
fibroma occurs at an earlier age and the
septa in an ameloblastoma are more
defined and coarse. In fact the septa in
ameloblastic fibroma are infrequent and
often very fine.
Giant cell granulomas --may appear
multilocular, but these tumors usually have
an epicenter anterior to the first molar
and the septa are characteristically
granular and ill defined.
Odontogenic myxomas-- can appear
multilocular but usually a few sharp straight septa can
be identified, which are not characteristic of
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Treatment. Ameloblastic fibromas are
benign, and the
rate of recurrence is low. A conservative
surgical
approach,including enucleation and
mechanical curet
tage of the surrounding bone,
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AMELOBLASTIC FIBRO-ODONTOMA
Definition
An ameloblastic fibro-odontoma is a mixed
tumor with
all the elements of an ameloblastic fibroma
but with
Scattered collections of enamel and
dentine
Clinical Features.The clinical features
are similar
to odontomas, often associated with a
missing tooth
or tooth that has failed to erupt.
This tumor appears during the same age
as odontomas and ameloblastic fibromas 56
Radiographic Features
Location-posterior aspect of the mandible.
The epicenter of the lesion is usually
occlusal to a developing tooth or toward
the alveolar crest.
Periphery. This tumor is usually well defined
and sometimes corticated.
Internal structure. The internal
structure is mixed, with the majority of the
lesion being radiolucent. Small lesions may
appear as enlarged follicles with only one or
two small,discrete radiopacities. Larger
lesions may have a more extensive calcified
internal structure
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Differential Diagnosis
Differentiation from a developing odontoma
may be difficult, but generally these tumors
have a greater soft tissue component
(radiolucent) than an odontoma
A complex odontoma, which shares a
common location, usually has one mass of
disorganized
tissue in the center, whereas the
ameloblastic fibroodontoma will usually have multiple
scattered mature
small pieces of dental hard tissue
Treatment
Usually conservative enucleation is used 58
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maxilla
The incisor canine-premolar region,
especially the canine region
Periphery. The usual radiographic
appearance is a welldefined corticated or sclerotic border.
Internal structure. Radiographically,
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Treatment
Conservative surgical excision is adequate
because the
tumor is not locally invasive,is well
encapsulated,and
is separated easily from the bone
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MESENCHYMAL TUMORS
(ODONTOGENIC
ECTOMESENCHYME)
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ODONTOGENIC MYXOMA
Synonyms
Myxoma, myxofibroma, and fibromyxoma
Definition
Odontogenic myxomas are uncommon,
accounting
for only 3% to 6% of odontogenic tumors.
They are benign, intraosseous neoplasms
that arise from odontogenic ectomesenchyme and resemble the
mesenchymal portion of the dental papilla
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Clinical features
Age - 10 to 30yrs.
Sex female
The tumor grows slowly and may or may
not cause pain.
Eventually it causes swelling and May
grow quite large if left untreated
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Radiographic Features
Location- mandible , the premolar and molar
areas
Periphery--The lesion usually is well
defined, and it may
have a corticated margin but most often
is poorly
defined, especially in the maxilla
Internal structure. majority have a mixed
radiolucent-radiopaque internal pattern.
Residual bone trapped within the tumor
will remodel
into curved and straight, course or fine
septa.The pres68
ence of these septa gives the tumor a
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Differential Diagnosis
Include ameloblastomas, central giant cell
granulomas, and central hemangiomas.
The finding of characteristic thin, straight
septa with less-than-expected bone
expansion is very useful in the differential.
Careful inspection of this area of expansion
will reveal a thin but intact outer cortex that
would not be seen in osteogenic sarcoma
Treatment
by resection with a generous amount of
surrounding bone to ensure removal of
myxomatous tumor that infiltrates the
adjacent marrow spaces.
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BENIGN CEMENTOBLASTOMA
Synonyms
Cementoblastoma and true cementoma
Definition
Benign cementoblastomas are slow-growing ,
mesenchymal neoplasms composed
principally of cementum
Clinical
Features
Age - 12 to 65
Sex - females
The tumor usually is a solitary lesion that
is slow-growing but that may eventually
displace teeth.
The involved tooth is vital and often
painful.
The pain seems to
vary from patient to patient and can be
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Radiographic Features
Location. mandible (78%) -premolar or first
molar(90%).
Periphery. The lesion is a well-defined
radiopacity with
a cortical border and then a well-defined
radiolucent
band just inside the cortical border
Internal structure. mixed radiolucentradiopaque lesions in which the majority
of the internal structure is radiopaque.
wheel spoke pattern
The density of the cemental mass usually
obscures the outline of the enveloped
root.
This central radiopaque mass as mentioned
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Clinical
Features
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NON
ODONTOGENIC
TUMORS
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Treatment
Excision is usually
choice
the
treatment
of
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NEUROFIBROMA
Synonym
Neurinoma
Definition
Neurofibromas are moderately firm,
benign, wellcircumscribed tumors caused by
proliferation of
Schwann cells in a disorderly pattern that
includes
portions of nerve fibers, such as peripheral
nerves,
Axons ,and connective tissue of the sheath of
Schwann.
As neurofibromas grow, they incorporate 86
Clinical Features
The central lesion of a neurofibroma maybe
the same
as the multiple lesions that develop in von
Recklinghausen's disease.
Neurofibromas can occur at any age but
usually are found in young patients.
Neurofibromas associated with the
mandibular nerve may produce pain or
paresthesia.
Neurofibromas also may expand and
perforate the cortex; causing swelling that is
hard or firm to palpation.
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Radiographic Features
Location. in the mandibular canal, in the
cancellous bone, and below the periosteum.
Periphery.. the margins of the radiolucency
in neurofibromas usually are sharply
defined and may be corticated.
However, despite the benign nature and
slow growth of the neurofibroma, some of
these lesions have indistinct margins.
Internal structure. The tumors usually
appear unilocular but on occasion may have a
multilocular appearance.
Effects on surrounding structures. A
neurofibroma of the inferior dental nerve
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Differential Diagnosis
Differentiation from other types of neural
lesions may
not be possible.
This tumor can be differentiated from
Vascular lesions because the expansion of
the canal is
in a fusiform shape,'whereas vascular
lesions enlarge
the whole canal and alter its path.
Treatment
Solitary central lesions that have been
excised seldom
recur. However, it is wise to re-examine the
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area peri-
NEUROFIBROMATOSIS
Synonym
von Reckling-hausen'sdisease
Definition
Neurofibromatosis
is a syndrome
consisting of cafe au-lait spots on the
skin, multiple peripheral nerve tumors,
and a variety of other dysplastic
abnormalities of the skin, nervous
system, bones, endocrine
organs, and
blood vessels
The two major classifications are
NF-1, a generalized form,
NF-2, a central form.
Oral lesion may occur as part of NF-1
or may be solitary and are called
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Clinical Features
Neurofibromatosis is one of the most
common genetic
Diseases.
The peripheral nerve tumors are of two
types, schwannomas and neurofibromas.
Most manifestations are appear gradually
during childhood & adult life. Cafe-au-Iait
spots become larger and more numerous with age; most patients eventually
have more than six spots larger than
1.5 cm in diameter.
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Radiographic features
The radiographic changes in the jaws with
neurofibroatosis
can be characteristic.
These changes include
1.enlargement
of the coronoid notch in
either or both the horizontal and
vertical dimensions
2. an obtuse angle between
the body
and the ramus
3. deformity
of the condylar head
4.lengthening of the condylar neck
5. lateral bowing
and thinning of the
ramus
6.enlargement
of the mandibular canal &
mental and mandibular foramina and an
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Treatment
Most patients live a normal life with Jew or
no symp toms. Small cutaneous and
subcutaneous neurofibromas can be removed if they are painful,
but large
plexiform neurofibromas should be left
alone.
Malignant conversion of these lesions has
occurred in rare cases.
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MESODERMAL TUMORS
OSTEOMA
Definition
Osteomas can form from membranous bones of
the
Skull and face.
The cause of the slowly growing osteoma is
obscure, but the tumor may arise from
cartilage or embryonal periosteum
It is not clearwhether osteomas are benign
neoplasms or hamartomas
Structurally, osteomas can be divided into
three- types: composed of compact bone (ivory),
composed of cancellous bone,
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composed of a combination of compact and
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Clinical
Features
Treatment
Unless the osteoma interferes with normal
function or
presents a cosmetic problem, this lesion
may not
require treatment. In such casesthe osteoma
should be
kept under observation.
Resection of osteoma sis possible and maybe
difficult if the osteoma is of the cortical
(ivory) type.
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CENTRAL HEMANGIOMA
Definition
A hemangioma is a proliferation of blood vessels
creating a mass that resembles a neoplasm ,
although in many cases it is actually a
hamartoma
Clinical
Features
Sturge-weberdimtri
syndrome
Kasabach
merritt
syndrome
Maffucci
syndrome
Von hippellindau
syndrome
Klippel
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Radiographic Features
Locotion. Mandible , posterior body and
ramus and within the inferior alveolar canal.
Periphery. In some instances the
periphery is well
defined and corticated, and in other cases it
maybe ill
defined and even simulate the appearance of
a malignant tumor
The formation of linear spicules of bone
emanating from the surface of the bone in a
sunray-like
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appearance can occur when the
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Differential Diagnosis
Hemangiomas should be considered in the
differential
Diagnosis of multilocular lesions involving
the body of
the ramus and body of the mandible.
Demonstration
of involvement of the inferior alveolar
canal is an
important indicator of a vascular lesion.
Treatment should be treated without delay,
because trauma that disrupts the
integrity of the
Affected jaw may result in lethal
exsanguination .Specifically, embolization (introduction of inert 111
ARTERIOVENOUS FISTULA
Synonyms
A-V defect, A-V shunt, A-V aneurysm,
and A-V
malformation
Definition
An arteriovenous (A-V) fistula, an uncommon
lesion , is
a direct communication between an artery
and a vein
that bypasses the intervening capillary
bed.
It usually results from trauma .
The head and neck are the most
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common sites.
Clinical Features
vary considerably, depending on the extent
of bone or soft tissue involvement.
The lesion may expand bone, and a mass
may be present in the Extraosseous soft
tissue.
The soft tissue swelling may have a purple
discoloration. Palpation or auscultation of
the swelling may reveal a pulse.
On the other hand,
neither the bone nor the soft tissue maybe
expanded,
and no pulse maybe clinically apparent.
Aspiration produces blood.
Recognition of the hemorrhagic nature of
these lesions is of utmost importance,
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Radiographic Features
Location.- ramus and retromolar area of the
mandible and involve the mandibular canal.
Periphery.The margins usually are well
defined and
corticated.
Internal structure. A tortuous path of an
enlarged vessel in bone may give a
multilocular appearance.
Otherwise the lesion is radiolucent.
Effects on surrounding structures. Both
central lesions
and those in adjacent soft tissue can erode bone,
resulting in well-defined (cystlike) lesions in the
bone.
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Treatment
An A-V aneurysmis treated surgically.
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REFERENCES
1.SHAFERS
ORAL PATHOLOGY
2.NEVILLE ORAL PATHOLOGY
3. ORAL radiology white & pharoah
4. burkets ORAL medicine
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