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Potential epithelial
sources include enamel
organ,odontogenic
rests(rests of
malassez,rests of
serres)reduced enamel
epithlium and the
epithelial lining of
odontogenic
cyst,especially the
dentigerous cyst
Ameloblastoma
Clinical features
There appears to be no gender predilection
It occurs predominantly in the fourth and fifth decades
The mandibular molar-ramus area is the most favored
site
Ameloblastomas are usually asymptomatic
Tooth movement or malocclusion may be the initial
presenting sign
Ameloblastoma
Clinical features
Rarely,extraosseous peripheral ameloblastomas
are found in the gingiva
They arise from dental lamina and often are
associated with impacted teeth in young patients
Radiographically,it appears as osteolytic
processes,may exhibits a unilocular or
multilocular appearance,root resorption may
appear
Ameloblastoma
Radiograph
unilocular appearance
root resorption
Benign mixed
tumor(pleomorphic adenoma)
It is the most common tumor of major and
minor salivary glands
The parotid gland accounts for
approximately 85% of these tumors
Of those tumors arising within the oral
cavity, the majority are noted in the hard
and soft palates
Benign mixed
tumor(pleomorphic adenoma)
The histogenesis of this lesion relates to a
simultaneous proliferation of variable
numbers of cells with ductal and
myoepithelial features
The risk of recurrence
It is difficult to distinguish from enlarged
lymph nodes within the submandibular
triangle
Benign mixed
tumor(pleomorphic adenoma)
Clinical features
They appear as firm,painless swellings and, in
the vast majority of cases, do not cause
ulceration of the overlying mucosa
When they arise within the parotid gland,
mixed tumors are generally painless, non-
tender, and slow growing, located below the
ear and posterior to the mandible
Benign mixed
tumor(pleomorphic adenoma)
Clinical features
The tumors may present below the angle of the
mandible and anterior to the sternocleidomastoid
muscle when they are situated within the inferior
pole or tail of the parotid
they generally range from a few millimeters to
several centimeters in diameter and are capable
of reaching giant proportions ,especially in the
parotid
Benign mixed
tumor(pleomorphic adenoma)
It is clinically impossible to distinguish
these from malignant salivary gland
tumors during early stages of growth
pleomorphic adenoma
Pleomorphic adenoma
of 19 years’
duration.despite its
large size, it did not
affect facial nerve
function,and the
patient concealed it
beneath her hair.
Malignant tumor of parotid
gland
Benign mixed
tumor(pleomorphic adenoma)
Malignant mixed tumor
Benign mixed
tumor(pleomorphic adenoma
Treatment
Enucleation of parotid mixed tumors is not
advisable because of risk of recurrence.
In most cases, superficial parotidectomy
with preservation of the facial nerve is the
most appropriate management for mixed
tumors arising within the parotid
Hemangiomas and vascular
malformations
Introduction
Vascular birthmarks,in the past named
“strawberry”or“capillary” hemangioma, “port-wine
stains,” “cavernous hemangiomas,”and “cystic
hygromas,”
Accurate description is crucial,since the prognosis and
management of vascular birthmarks depend on their
correct classification as hemangiomas or malformations
Hemangiomas and vascular
malformations
Introduction
Their distinctions have been clarified on the basis of cellular
and clinical characteristics.
Hemangiomas have an increased mitotic activity and as such
may be considered true neoplasms. they are typically absent
at birth or as a faint vascular blush.during the first several
months of life they may undergo a rapid proliferative phase,
during which they sometimes grow to large size. The
majority of Hemangiomas undergo spontaneous involution
by the age of seven
Hemangiomas and vascular
malformations
Introduction
vascular malformations have a normal rate of
endothelial cell turnover. They result from congenital
errors in vascular morphogenesis and are classified by
their vessel of involvement–
capillary,venous,arterial,lymphatic, or combined. They
normally grow proportionally with the child and do not
regress spontaneously, unlike Hemangiomas
Lymphatic malformations(cystic hygromas) classically
occur in the neck or the floor of the mouth.
Hemangiomas and vascular
malformations
surgical resection
Photodynamic laser therapy
Intralesional steroid injections or
sclerosing agents
Systemic dexamethasone therapy, or the
intravenous administration of interferon-a
Hemangiomas
cheek
Hemangiomas
tongue
Hemangiomas
the lower lip
Cystic hygroma
surgical resection
Indications for early surgical resection
include ulceration and bleeding,
obstruction of the eye with subsequent
amblyopia, nasal airway obstruction
Treatment of Hemangiomas
Epithelial tumors
Ameloblastoma
Squamous odontogenic tumor
Calcifying Epithelial Odontogenic tumor
Clear cell Odontogenic tumor
Odontogenic tumors
Mesenchymal tumors
Odontogenic Myxoma
Central Odontogenic Fibroma
Cementoblastoma
Periapical Emental Dysplasia
Mixed tumors(Epithelial and Mesenchymal)
Odontoma
Ameloblastic fibroma and Ameloblastic fibroodontoma
Malignant tumors
Introduction
Malignant neoplasms that arise in the head and
neck area or upper aerodigestive tract share the
general behavior of most solid tumors:local
growth, locoregional spread, and distant
metastasis.
Unlike most other solid tumors, 60 percent of
patients with a fatal head and neck malignancy
die without clinical evidence of metastasis
beyond the local (regional) disease.
Malignant tumors
Introduction
Central nervous system invasion, rupture of the
great vessels,airway obstruction, and invasive
local infection are common causes of death on
these patients
Because of the predominant local and
locoregional natural history of this disease,
significant attention must be paid to local
diagnosis and therapy
Squamous cell carcinoma
Introduction
Accounts for about 90 percent of all oral
malignancies
Over 90 percent of cases occur in patients over
the age of 40 years
Oral carcinoma may occur on any part of the oral
mucosa(lip, tongue, the floor of the mouth, the
buccal mucosa, the alveolar ridge, and the palate)
Squamous cell carcinoma
Clinical presentation
Early lesions are usually asymptomatic and
have a variable appearance
Common modes of presentation are a
white patch, a small exophytic growth(no
ulceration or erythema), a small indolent
ulcer, or an area of erythroplakia
Pain is seldom present
Squamous cell carcinoma
Clinical presentation
Persistent ulceration, induration and fixation of
affected tissue to underlying structures, and
underlying bone destruction in the case of
alveolar lesions
An advanced lesion may present as a broad
based, exophytic mass with a rough nodular,
warty, hemorrhagic or necrotic surface, or as a
deeply destructive and crater-like ulcer with
raised,rolled everted edges
Squamous cell carcinoma
Clinical presentation
Pain may be a feature of an advanced lesion.
Bone invasion may be detected on radiographs
but may be suggested clinically by mobility of
teeth and in the case of mandible by altered
sensation over the distribution of the mental
nerve, or pathological fracture
Squamous cell carcinoma
Clinical symptoms
X-ray examination
biopsy
Squamous carcinoma
Tobacco,alcohol, chronic
irritation from jagged teeth or
dental appliances are the most
common factors
Occurs at the midportion of
the lateral tongue
Exophytic growth with
nodular surface
Cervical metastases is present
in 40 to 61 percent of patients
Squamous cell carcinoma
Floor of mouth
13 to 17 percent of oral
lesions arise in this area
Crater-liked ulcer with
raised, rolled, everted
edges
Cervical metastases are
frequent
Squamous cell carcinoma
Floor of mouth
Maxillary sinuses
Late-stage disease
Nasal obstruction
Local pain
Epistaxis
Cheek swelling
Loosening of maxillary
teeth
Paresthesias
Double vision
Maxillary sinuses
(CT scan)
Treatment
A benign fibrous
tissue tumor arising
from the periodontal
membrane or
nearby periosteum
A smooth, firm,
slowly growing
lump,covered with
normal gingiva
Fibrous epulis
Usually emerges
between two teeth,
which may be pushed
apart by pressure
Treatment:local
excision with curettage
of the origin.otherwise,
it may recur