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CLASSIFICATION
I . Tumours of odontogenic epithelium
1. Ameloblastoma
•Malignant ameloblastoma
•Ameloblastic carcinoma
2. Calcifying epithelial odontogenic tumor
3. Squamous odontogenic tumor
4. Clear cell odontogenic carcinoma
5. Primary intraosseous carcinoma
II . mixed odontogenic tumours
1. Ameloblastic fibroma
2. Ameloblastic fibro-odontoma
3. Ameloblastic fibrosarcoma
4. Odontoameloblastoma
5. Odontoma
•Compound composite
•Complex composite
6 Adenomatoid odontogenic tumor
III . Tumours of odontogenic ectomesenchyme
1. Odontogenic fibroma
2. Granular cell odontogenic tumor
3. Odontogenic myxoma
4. Cementoblastoma
AMELOBLASTOMA
 common epithelial odontogenic tumor
 Benign, but locally invasive
 Asymptomatic and remain undiscoverd until growth
produce expantion ,tooth and dental occlusion
disturbances, or incidental radiograph reveal the
lesion
 In some rare cases paresthesia and pain may occur
and associated with root resorption and tooth
displacement
 Most commonly forms in posterior mandible
 age at which lesion became clinically evident is third
to fifth decade
 Inadequate treatment usually followed by aggressive
recurrence
CLINICAL PRESENTATION OF AMELOBLASTOMA
SUBTYPES OF AMELOBLASTOMA
Multicystic (multilocular) and solid
(86%)
Unicystic (unilocular) (13%)
peripheral (extraosseous) (1%)
MULTICYSTIC AMELOBLASTOMA
Clinically
 is the most common form of this lesion, nearly
occur in patients over 25 years of age. With no
sex predilection
 The lesion may cause extensive deformities of
the mand. & max.
 It is most commonly located in the mand , with
75% occurring in the molar & ascending ramus
area.
 The tumor is slowly growing, locally
aggressive, allows time for periosteum to
produce a thin shell of bone which cracks
easily when palpated
known as ( eggshell cracking).
RADIOGARAPHICALLY
 Classic–multilocular radiolucency of
posterior mandible.
 Well-circumscribed, soap-bubble
appearance
 Unilocular – often confused with
odontogenic cysts
 Root resorption –usually associated
with Malignancy
HISTOPATHOLOGY
 Two main patterns – plexiform and follicular , and other rare
types
acanthomatous, granular cell,desmoplastic,basal cell
 Classic – sheets and islands of tumor cells,
 outer rim of ameloblasts is polarized away
from basement membrane
 Center looks like stellate reticulum
 Squamous differentiation (1%) – Diagnosed
as ameloblastic carcinoma
UNICYSTIC AMELOBLASTOMA
 Mostly found within the lining of a large
unilocular cyst specially the Dentigerous cyst.
 commonly associated with the crown of an
impacted tooth in a young patient.
 Average age 23 years
 90% in mandible (usually posterior regions)
 Asymptomatic but may cause painless swelling
RADIOGRAPHICALLY
 Typically appears as circumscribed Unilocular radiolucency
that surrounds the crown of unerupted mandibular third
molar.
or multilocular (25%) radiolucency .
HISTOPATHOLOGY:
 The lesion composed of island of epith.
which may be follicular or plexiform
within the epith. lining of the cystic
wall.
 Some lesions will contain areas in
which the epith. Is thickened with
papillary projections extending into the
lumen, this called “intraluminal
unicystic ameloblastoma”
 When the thickened lining penetrates
the adjacent capsular tissue, it’s termed
“mural unicystic ameloblastoma.
PERIPHERAL AMELOBLASTOMA
(EXTRAOSSEOUS)
 very uncommon
 histologically similar to the
intraosseous common
ameloblastoma but is limited
to the soft tissues of the
gingiva.
TREATMENT
 Treatment range from simple enucleation and curretage to block
resection.
 recurrency reported in 55% to 100% for multicystic lesion and about
18 to 35% for unicystic lesion after curretage or enucleation
 curettage can disperse the tumor into uninvolved areas
 The best chance for completely removing the lesion is by marginal block
resection with 1,5 to 2 cm safe margin for multicystic lesion
and 1 to 1,5 cm for unicystic and peripheral lesions.
 Because children and adolescents with ameloblastoma are still
developing physically and psychologically, Conservative
treatment can get good results .
 nonresectable ameloblastoma can be treated by Radiotherapy.
 Long term followup up to 20 years and even more required.
MALIGNANT AMELOBLASTOMA
 It is benign ameloblastoma of jaws but show metastatic growth.
 metastasis may occure to the hip ,vertebrae,brain,kidney and even
myocardium but The most common sites for metastasis are the lungs
 Lung metastases regarded as aspiration phenomena, while the
peripheral location of many of these deposits supports hematogenous
spread.
 metastasis usually associated with multicystic ameloblastomas rather
than unicystic tumors.
 Hypercalcemia may be a marker of metastatic disease in some
instances
due to production of parathyroid –related protein (PTHrP) by metastatic
AMELOBLASTIC CARCINOMA
 An ameloblastoma that has cytological
features of malignancy
 Although ameloblastic carcinomas
have been reported to metastasize to
the lungs and distant organs many
cases do not metastasize.
 rapid growth and pain were common
symptoms.
 The treatment is similar to that of an
intraosseous carcinoma but the
prognosis is poor if metastases are
present.
CALCIFYING EPITHELIAL ODONTOGENIC TUMOUR
(PINDBORG TUMOR)
 uncommon epithelial lesion that
accounts for < 1% of all odontogenic
tumors.
 most often in patients between 30 and
50 years of age with no gender
predilection
 Approximately two-thirds of these
neoplasms occur in the mandible
 A painless slow-growing mass is the
most common presenting sign
 Locally invasive but does not metastasis
RADIOGRAPHICALLY
 most common presentation is a mixed
radiopaque/radiolucent lesion, frequently associated with an
impacted tooth
HISTOPATHOLOGY
 the Pindborg tumor is quite unique.
 islands, strands, or sheets of epithelial
cells in a fibrous stroma .
 Large areas of amorphous eosinophilic
hyalinized (amyloid-like) material are also
present.
 Some cases show clear cells ,prominent
clear cells associated with increased the
aggressiveness of the lesion.
 Calcifications, which are a distinctive
feature of the tumor, develop within the
amyloid-like material and form concentric
rings, known as
Liesegang rings
TREATMENT
 tumor is generally recommended to be treated identically to the
ameloblastoma and odontogenic myxoma,
 with 1.0 to 1,5 cm bony linear margins and the appropriate
attention to soft tissue anatomic barriers .
 Small lesions can be treated by enucleation followed by vigorous
curettage .
 The prognosis of CEOT is good with infrequent recurrence . the
recurrence rate about 14 % and recurrent lesion may not be
manifested for many years.
 Tumors with more amyloid and calcified content tend to have
better prognosis in compare to that of clear cell variant .
CLEAR CELL ODONTOGENIC CARCINOMA
 a rare epithelial odontogenic tumor
associated with aggressive clinical
behavior with metastasis and low survival
rate.
 The classic clinical presentation of CCOC
is a painful anterior mandibular swelling in
an elderly women.
 characterised by sheets and islands of
vacuolated and clear cells which not stain
in histological preparation because of rich
glycogen giving an empty appearance .
TREATMENT
 Tumor may be aggressive and are capable of local recurrence, as well
as regional and distant metastasis
 Such tumors should be treated by wide en-bloc resection with long-
term follow-up
 In the presence of clinical and/or radiographic evidence of nodal
metastases, neck dissection should also be performed .
PRIMARY INTRAOSSEOUS SQUAMOUS CELL
CARCINOMA
 it is rare epithelial odontogenic
tumor
 assumed to arise from odontogenic
epithelium or linings of odontogenic
cysts.
 It may be solid or cystogenic
 typically occur in the posterior region
of mandible of elderly male .
 Pain and paresthesia may occur
 Radiographically variable depending
on the progression of the disease
from outlined radiolucencies to
diffusely infiltrative lesions
TREATMENT
 The prognosis
associated with PIOC
of the jaws is poor and
suggests the need for
aggressive treatment
 Treated by resection
followed by
postoperative
radiotherapy .
ODONTOMA
 are developmental
malformations(hamartomas) of dental
tissues.
 Odontomas are the most frequently
occurring odontogenic tumors, with
prevalence exceeding that of all other
odontogenic tumors combined.
 Usually found between ages 10 and 20
years with no gender predilection
 May be compound or complex
 Impaction of permanent teeth was the
most common complication associated
with odontoma
COMPOUND ODONTOMA
 many small teeth
 Most common sites are
anterior maxilla
COMPLEX ODONTOMA
 disordered mass of dental hard
tissue
 Most common site are posterior
mandible or maxilla
Treatment ;
Odontomas are treated with simple
enucleation and curettage .
Not known to recur .
ODONTOGENIC MYXOMA
 Rare ectomesenchymal Neoplasm
 histologically resembles the dental papilla of
the developing tooth.
 Usually seen in young adults
 Radiographically, the odontogenic myxoma
appears as a unilocular or multilocular
radiolucency that may displace or cause
root resorption of teeth in the area of the
tumor
 In some patients the tumor may have a
greater tendency to form collagen fibers;
such lesions are designated as
fibromyxomas
 slow growing with a potential for aggressive
behavior and a high recurrence rate after
subtherapeutic removal.
TREATMENT
 These tumors are not encapsulated and tend to infiltrate the
surrounding bone such that complete removal by curettage
is nearly impossible.
 Odontogenic myxomas should be treated with resection with
1.0 cm bony linear margins as confirmed with a specimen
radiograph or frozen section .
 Treated by excision with a small margin Can undergo
malignant changes
AMELOBLASTIC FIBROMA
 Rare mixed odontogenic tumor
 Usually seen in children or young adults
 the posterior mandible is affected in 70%
of cases
 Solid lesion but appears as unilocular or
multilocular radiolucency
 Treated by excision with small margin
 Huge lesions especially which appear
Multilocular are best treated by resection
without continuity
AMELOBLASTIC SARCOMA
(AMELOBLASTIC FIBROSARCOMA)
 it is rare mixed malignant odontogenic tumor .
 It is invasive and destructive but has little tendency to
metastasise.
 Reports suggest that approximately 50% arise from ameloblastic
fibromas.
 Radiographically appear as ill-defined destructive radiolucent
lesion
 Local excision usually followed by rapid recurrence so it is best
treated by radical surgical excision
ODONTO-AMELOBLASTOMA ; (AMELOBLASTIC ODONTOMA)
 Extremly rare mixed odontogenic
tumour
 More in mandible of younger patients
 pain ,delayed eruption of teeth ,
expantion of affecting bone may
occur
 Radiographically show radiolucency
with calcified structures
 Treated similar to ameloblastoma
because local excision usually
followed by multiple recurrence
ADENOMATOID ODONTOGENIC TUMOR
ADENOAMELOBLASTOMA,GLANDULAR AMELOBLASTOMA,ADENOMATOID AMELOBLASTOMA
 Some consider it as a hamartoma
 uncommon , accounting for 3 to 7% of all
odontogenic tumors.
 limited to young ,extremely uncommon in
patients > 30 years.
 Maxilla > mandible
 Anterior region > posterior region
 Female > male
 rarely exceeding 3 cm in diameter
 lesion appears as a well-circumscribed
unilocular radiolucency that involves the crown
of an erupted tooth, frequently a
canine.radiolucency extend beyond the
cemento-enamel junction
TREATMENT
 Histologically, the adenomatoid odontogenic tumor is a well-defined lesion
that is usually surrounded by a thick fibrous capsule
 Owing to this lesion being encapsulated, it separates easily from the
surrounding bone.As such, an enucleation and curettage surgery is
curative
ODONTOGENIC FIBROMA
 rare ectomesenchymal odontogenic
tumour
 Clinically, It forms a slow-growing
asymptomatic mass which may eventually
expand the jaw.
 radiographically , it appears as a sharply
defined, radiolucent area in a tooth-bearing
region.
 Calcifications composed of cementum-like
material or dentinoid are present in some
cases
 Odontogenic fibromas are benign and
shell out from their surrounding tissues .
CEMENTOBLASTOMA
 benign ectomesenchymal neoplasm of
cementum and forms a mass of cementum-
like tissue as an irregular or rounded mass
attached to the root of a tooth, usually a
mandibular first molar.
 mainly affect young adults, particularly
males.
 They are slow-growing and the jaw is not
usually expanded. And may rarely causes
gross bony swelling and pain
 Radiographically, there is typically a
radiopaque mass with thin radiolucent
margin, attached to the roots of a tooth.
 Resorption of related roots is common, but
Treatment ; by enucleation
References :
Neville, Oral and Maxillofacial Pathology, 2nd
Ed
cawsin Essentials of Oral Pathology and Oral
Medicine ,7th Ed
Peterson's Principles of Oral and Maxillofacial
Surgery 2nd Ed 2004
Oral and Maxillofacial Surgery, Raymond J.
Fonseca
World Health Organization (WHO)
Classification of Tumours , IARCPress
Lyon, 2005
‫لادي‬‫ب‬‫ن‬‫م‬‫ورة‬‫ص‬//‫ة‬‫ن‬‫ي‬‫د‬‫ح‬‫ة‬‫ن‬‫ي‬‫د‬‫م‬

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Odontogenic tumors

  • 2.
  • 3.
  • 4. CLASSIFICATION I . Tumours of odontogenic epithelium 1. Ameloblastoma •Malignant ameloblastoma •Ameloblastic carcinoma 2. Calcifying epithelial odontogenic tumor 3. Squamous odontogenic tumor 4. Clear cell odontogenic carcinoma 5. Primary intraosseous carcinoma II . mixed odontogenic tumours 1. Ameloblastic fibroma 2. Ameloblastic fibro-odontoma 3. Ameloblastic fibrosarcoma 4. Odontoameloblastoma 5. Odontoma •Compound composite •Complex composite 6 Adenomatoid odontogenic tumor III . Tumours of odontogenic ectomesenchyme 1. Odontogenic fibroma 2. Granular cell odontogenic tumor 3. Odontogenic myxoma 4. Cementoblastoma
  • 5.
  • 6. AMELOBLASTOMA  common epithelial odontogenic tumor  Benign, but locally invasive  Asymptomatic and remain undiscoverd until growth produce expantion ,tooth and dental occlusion disturbances, or incidental radiograph reveal the lesion  In some rare cases paresthesia and pain may occur and associated with root resorption and tooth displacement  Most commonly forms in posterior mandible  age at which lesion became clinically evident is third to fifth decade  Inadequate treatment usually followed by aggressive recurrence
  • 7. CLINICAL PRESENTATION OF AMELOBLASTOMA
  • 8.
  • 9.
  • 10. SUBTYPES OF AMELOBLASTOMA Multicystic (multilocular) and solid (86%) Unicystic (unilocular) (13%) peripheral (extraosseous) (1%)
  • 11. MULTICYSTIC AMELOBLASTOMA Clinically  is the most common form of this lesion, nearly occur in patients over 25 years of age. With no sex predilection  The lesion may cause extensive deformities of the mand. & max.  It is most commonly located in the mand , with 75% occurring in the molar & ascending ramus area.  The tumor is slowly growing, locally aggressive, allows time for periosteum to produce a thin shell of bone which cracks easily when palpated known as ( eggshell cracking).
  • 12. RADIOGARAPHICALLY  Classic–multilocular radiolucency of posterior mandible.  Well-circumscribed, soap-bubble appearance  Unilocular – often confused with odontogenic cysts  Root resorption –usually associated with Malignancy
  • 13. HISTOPATHOLOGY  Two main patterns – plexiform and follicular , and other rare types acanthomatous, granular cell,desmoplastic,basal cell  Classic – sheets and islands of tumor cells,  outer rim of ameloblasts is polarized away from basement membrane  Center looks like stellate reticulum  Squamous differentiation (1%) – Diagnosed as ameloblastic carcinoma
  • 14.
  • 15.
  • 16.
  • 17. UNICYSTIC AMELOBLASTOMA  Mostly found within the lining of a large unilocular cyst specially the Dentigerous cyst.  commonly associated with the crown of an impacted tooth in a young patient.  Average age 23 years  90% in mandible (usually posterior regions)  Asymptomatic but may cause painless swelling
  • 18. RADIOGRAPHICALLY  Typically appears as circumscribed Unilocular radiolucency that surrounds the crown of unerupted mandibular third molar. or multilocular (25%) radiolucency .
  • 19.
  • 20. HISTOPATHOLOGY:  The lesion composed of island of epith. which may be follicular or plexiform within the epith. lining of the cystic wall.  Some lesions will contain areas in which the epith. Is thickened with papillary projections extending into the lumen, this called “intraluminal unicystic ameloblastoma”  When the thickened lining penetrates the adjacent capsular tissue, it’s termed “mural unicystic ameloblastoma.
  • 21. PERIPHERAL AMELOBLASTOMA (EXTRAOSSEOUS)  very uncommon  histologically similar to the intraosseous common ameloblastoma but is limited to the soft tissues of the gingiva.
  • 22. TREATMENT  Treatment range from simple enucleation and curretage to block resection.  recurrency reported in 55% to 100% for multicystic lesion and about 18 to 35% for unicystic lesion after curretage or enucleation  curettage can disperse the tumor into uninvolved areas  The best chance for completely removing the lesion is by marginal block resection with 1,5 to 2 cm safe margin for multicystic lesion and 1 to 1,5 cm for unicystic and peripheral lesions.  Because children and adolescents with ameloblastoma are still developing physically and psychologically, Conservative treatment can get good results .  nonresectable ameloblastoma can be treated by Radiotherapy.  Long term followup up to 20 years and even more required.
  • 23. MALIGNANT AMELOBLASTOMA  It is benign ameloblastoma of jaws but show metastatic growth.  metastasis may occure to the hip ,vertebrae,brain,kidney and even myocardium but The most common sites for metastasis are the lungs  Lung metastases regarded as aspiration phenomena, while the peripheral location of many of these deposits supports hematogenous spread.  metastasis usually associated with multicystic ameloblastomas rather than unicystic tumors.  Hypercalcemia may be a marker of metastatic disease in some instances due to production of parathyroid –related protein (PTHrP) by metastatic
  • 24. AMELOBLASTIC CARCINOMA  An ameloblastoma that has cytological features of malignancy  Although ameloblastic carcinomas have been reported to metastasize to the lungs and distant organs many cases do not metastasize.  rapid growth and pain were common symptoms.  The treatment is similar to that of an intraosseous carcinoma but the prognosis is poor if metastases are present.
  • 25. CALCIFYING EPITHELIAL ODONTOGENIC TUMOUR (PINDBORG TUMOR)  uncommon epithelial lesion that accounts for < 1% of all odontogenic tumors.  most often in patients between 30 and 50 years of age with no gender predilection  Approximately two-thirds of these neoplasms occur in the mandible  A painless slow-growing mass is the most common presenting sign  Locally invasive but does not metastasis
  • 26. RADIOGRAPHICALLY  most common presentation is a mixed radiopaque/radiolucent lesion, frequently associated with an impacted tooth
  • 27. HISTOPATHOLOGY  the Pindborg tumor is quite unique.  islands, strands, or sheets of epithelial cells in a fibrous stroma .  Large areas of amorphous eosinophilic hyalinized (amyloid-like) material are also present.  Some cases show clear cells ,prominent clear cells associated with increased the aggressiveness of the lesion.  Calcifications, which are a distinctive feature of the tumor, develop within the amyloid-like material and form concentric rings, known as Liesegang rings
  • 28. TREATMENT  tumor is generally recommended to be treated identically to the ameloblastoma and odontogenic myxoma,  with 1.0 to 1,5 cm bony linear margins and the appropriate attention to soft tissue anatomic barriers .  Small lesions can be treated by enucleation followed by vigorous curettage .  The prognosis of CEOT is good with infrequent recurrence . the recurrence rate about 14 % and recurrent lesion may not be manifested for many years.  Tumors with more amyloid and calcified content tend to have better prognosis in compare to that of clear cell variant .
  • 29. CLEAR CELL ODONTOGENIC CARCINOMA  a rare epithelial odontogenic tumor associated with aggressive clinical behavior with metastasis and low survival rate.  The classic clinical presentation of CCOC is a painful anterior mandibular swelling in an elderly women.  characterised by sheets and islands of vacuolated and clear cells which not stain in histological preparation because of rich glycogen giving an empty appearance .
  • 30. TREATMENT  Tumor may be aggressive and are capable of local recurrence, as well as regional and distant metastasis  Such tumors should be treated by wide en-bloc resection with long- term follow-up  In the presence of clinical and/or radiographic evidence of nodal metastases, neck dissection should also be performed .
  • 31. PRIMARY INTRAOSSEOUS SQUAMOUS CELL CARCINOMA  it is rare epithelial odontogenic tumor  assumed to arise from odontogenic epithelium or linings of odontogenic cysts.  It may be solid or cystogenic  typically occur in the posterior region of mandible of elderly male .  Pain and paresthesia may occur  Radiographically variable depending on the progression of the disease from outlined radiolucencies to diffusely infiltrative lesions
  • 32.
  • 33. TREATMENT  The prognosis associated with PIOC of the jaws is poor and suggests the need for aggressive treatment  Treated by resection followed by postoperative radiotherapy .
  • 34. ODONTOMA  are developmental malformations(hamartomas) of dental tissues.  Odontomas are the most frequently occurring odontogenic tumors, with prevalence exceeding that of all other odontogenic tumors combined.  Usually found between ages 10 and 20 years with no gender predilection  May be compound or complex  Impaction of permanent teeth was the most common complication associated with odontoma
  • 35. COMPOUND ODONTOMA  many small teeth  Most common sites are anterior maxilla
  • 36. COMPLEX ODONTOMA  disordered mass of dental hard tissue  Most common site are posterior mandible or maxilla
  • 37. Treatment ; Odontomas are treated with simple enucleation and curettage . Not known to recur .
  • 38. ODONTOGENIC MYXOMA  Rare ectomesenchymal Neoplasm  histologically resembles the dental papilla of the developing tooth.  Usually seen in young adults  Radiographically, the odontogenic myxoma appears as a unilocular or multilocular radiolucency that may displace or cause root resorption of teeth in the area of the tumor  In some patients the tumor may have a greater tendency to form collagen fibers; such lesions are designated as fibromyxomas  slow growing with a potential for aggressive behavior and a high recurrence rate after subtherapeutic removal.
  • 39. TREATMENT  These tumors are not encapsulated and tend to infiltrate the surrounding bone such that complete removal by curettage is nearly impossible.  Odontogenic myxomas should be treated with resection with 1.0 cm bony linear margins as confirmed with a specimen radiograph or frozen section .  Treated by excision with a small margin Can undergo malignant changes
  • 40. AMELOBLASTIC FIBROMA  Rare mixed odontogenic tumor  Usually seen in children or young adults  the posterior mandible is affected in 70% of cases  Solid lesion but appears as unilocular or multilocular radiolucency  Treated by excision with small margin  Huge lesions especially which appear Multilocular are best treated by resection without continuity
  • 41. AMELOBLASTIC SARCOMA (AMELOBLASTIC FIBROSARCOMA)  it is rare mixed malignant odontogenic tumor .  It is invasive and destructive but has little tendency to metastasise.  Reports suggest that approximately 50% arise from ameloblastic fibromas.  Radiographically appear as ill-defined destructive radiolucent lesion  Local excision usually followed by rapid recurrence so it is best treated by radical surgical excision
  • 42. ODONTO-AMELOBLASTOMA ; (AMELOBLASTIC ODONTOMA)  Extremly rare mixed odontogenic tumour  More in mandible of younger patients  pain ,delayed eruption of teeth , expantion of affecting bone may occur  Radiographically show radiolucency with calcified structures  Treated similar to ameloblastoma because local excision usually followed by multiple recurrence
  • 43. ADENOMATOID ODONTOGENIC TUMOR ADENOAMELOBLASTOMA,GLANDULAR AMELOBLASTOMA,ADENOMATOID AMELOBLASTOMA  Some consider it as a hamartoma  uncommon , accounting for 3 to 7% of all odontogenic tumors.  limited to young ,extremely uncommon in patients > 30 years.  Maxilla > mandible  Anterior region > posterior region  Female > male  rarely exceeding 3 cm in diameter  lesion appears as a well-circumscribed unilocular radiolucency that involves the crown of an erupted tooth, frequently a canine.radiolucency extend beyond the cemento-enamel junction
  • 44. TREATMENT  Histologically, the adenomatoid odontogenic tumor is a well-defined lesion that is usually surrounded by a thick fibrous capsule  Owing to this lesion being encapsulated, it separates easily from the surrounding bone.As such, an enucleation and curettage surgery is curative
  • 45. ODONTOGENIC FIBROMA  rare ectomesenchymal odontogenic tumour  Clinically, It forms a slow-growing asymptomatic mass which may eventually expand the jaw.  radiographically , it appears as a sharply defined, radiolucent area in a tooth-bearing region.  Calcifications composed of cementum-like material or dentinoid are present in some cases  Odontogenic fibromas are benign and shell out from their surrounding tissues .
  • 46. CEMENTOBLASTOMA  benign ectomesenchymal neoplasm of cementum and forms a mass of cementum- like tissue as an irregular or rounded mass attached to the root of a tooth, usually a mandibular first molar.  mainly affect young adults, particularly males.  They are slow-growing and the jaw is not usually expanded. And may rarely causes gross bony swelling and pain  Radiographically, there is typically a radiopaque mass with thin radiolucent margin, attached to the roots of a tooth.  Resorption of related roots is common, but
  • 47. Treatment ; by enucleation
  • 48. References : Neville, Oral and Maxillofacial Pathology, 2nd Ed cawsin Essentials of Oral Pathology and Oral Medicine ,7th Ed Peterson's Principles of Oral and Maxillofacial Surgery 2nd Ed 2004 Oral and Maxillofacial Surgery, Raymond J. Fonseca World Health Organization (WHO) Classification of Tumours , IARCPress Lyon, 2005