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ODONTOGENIC TUMORS
- AMELOBLASTOMA -
Dr.MANOJ KUMAR
INTRODUCTION
The permutation of
different cells of
different origin makes
odontogenic tumors a
highly complicated
group of lesions
EPITHELIAL ODONTOGENIC TUMORS
1. Minimal inductive change in CT
 Ameloblastoma.
 CEOT (Pindborg’s)
 AOT
2. Extensive inductive changes in connective tissue
 Ameloblastic fibroma
 Ameloblastic fibro-odontoma
 Odoto- Ameloblastoma
 Odontoma – Complex
Compound
MESODERMAL ODONTOGENIC TUMOURS
 Central odontogenic fibroma
 Odontogenic myxoma
 Cementoma –
• Periapical cemental dysplasia
• Cementifying fibroma
• Benign cementoblastoma
 Dentinoma
Malignant odontogenic tumors
– Odontogenic carcinoma
• Primary intraosseous carcinoma
• Malignant Ameloblastoma
– Odontogenic Sarcoma
• Ameloblastic Fibrosarcoma
• Ameloblastic Odontosarcoma
AMELOBLASTOMA
WHO (1992)
“Is a true neoplasm of enamel organ like
tissue which does not undergo
differentiation to the point of enamel
formation”
Robinson described it as
A tumour that is usually unicentric,
nonfunctional intermittent in growth
anatomically benign clinically persistent
Synonyms :
 Admantinoma
 Multilocular cyst
 Admantoblastoma
 Eve’s Diesease
History :
• CUZACK (1827)- First Recognized
• FALKSON (1879) – Description
• MALASSEZ (1885) – Admantinoma
• IVY &CHURCHILL (1934) – Ameloblastoma
• Unicystic ameloblastoma – Robinson and
Martinez in 1977
ORIGIN
• Cell rests of enamel organ
– Dental lamina remnants
– Hertwig’s sheath
– Rests of malassez
• Epithelium of Odontogenic cysts (Dentigerous cyst &
Odontomas)
• Disturbances in developing enamel organ.
• Heterotropic epithelium in other parts of the body,
especially the Pituitary Gland.
• Basal cells of oral epithelium.
extra osseous
• Dental lamina
ameloblast
• Oral epithelium
Incidence
 1% of oral tumors
 18-20% of odontogenic
tumors
Clinical features
 20-50 years
 Number of cases reported in
children
 Youngest reported one month old
 Oldest 98 yrs
 Frequent in
mandible than
maxilla
 3:1
Signs & symptoms
 Asymptomatic
 Asymmetry
 Slow growing – non
tender
 Later stages pain
 Secondary infection
 Ulceration
 Egg shell crackling
 Extra osseous Small nodule
Classification
Robinson and Martinez 1977
Anatomic site
1. Central /intraosseous
i. Multicystic/Conventional
ii. Unicystic
iii.solid
2. Peripheral/ extra osseous
Radiological features
• Numerous well defined radioluscency of varying
diameter
• Honey comb
• Soap bubble appearance
• Unicystic radiolucent lesion indistinguishable
with cysts
Ameloblastoma
With in medullary cavity
Scalloping of inner cortex
Pressure erosion
Shell remains
C T SCAN
 When maxillary sinus involved
 Cloudiness of sinus
 Destruction of wall
 Unicystic in maxilla
Histopathology
• Follicular
• Plexiform
• Acanthomatous
• Granular cell
• Desmoplastic
• Basal cell type
Follicular
Plexiform
Acanthomatous
Granular cell
Desmoplastic
Basal cell
Unicystic ameloblastoma
Ackerman in 1988
1. Type-I Luminal (consisted of unilocular cystic lesions lined by
epithelium exhibiting features of ameloblastoma).
1. Type-II Intra luminal (showed epithelial nodules arising from
the cystic lining and projecting into the cyst lumen. These
nodules comprised epithelium with a plexiform or follicular
pattern resembling that seen in intraosseous ameloblastoma.).
1. Type-III Mural ameloblastoma (characterized by the presence of
invasive islands of ameloblastomatous epithelium in the
connective tissue wall of the cyst, and these islands may or may
not be connected to the cyst lining)
Mural Ameloblastoma
Peripheral ameloblastoma
• Peripheral ameloblastoma (PA) is a rare odontogenic tumor that
accounts for 1% for all ameloblastomas.
• Kuri first reported PA in 1911
• In 1959, Stanley and Krogh defined the clinical and histopathologic
characteristics.
• The strict definition of PA according to Buchner and Scuibba (1987)
excludes lesions in extragingival locations.
The etiology of PA is unclear. The tumor can derive from the extraosseous
epithelial remnants of the dental lamina or from the basal cell layer of the
oral mucosa, which is believed to have odontogenic potential
• The differential diagnosis usually includes
– Pyogenic granuloma, peripheral
– Giant cell granuloma,
– Peripheral odontogenic fibroma,
– Peripheral ossifying fibroma,
– Papilloma,
– Epulis.
• Only four cases of malignant PA have been
reported to date.
Pitutary ameloblastoma
• Craniopharyngioma
• Rathke’s pouch tumor
DIFFERENTIAL DIAGNOSIS
–Multilocular cyst
Dentigerous cyst
Odontogenic kerato cyst
–Giant cell granuloma, cherubism
–Brown’s tumor
–Central hemangioma
–Odontogenic myxoma
Treatment
–Behavior and potential of tumor
–Growth characteristics
–Anatomic site
–Clinical extent
–Size of tumor
–Histologic pattern
Less than complete
excision is equivalent to
planned recurrence
General principles
1. Definitive & offer best cure
2. Curettage and enucleation – recurrence
3. Curettage condemned
4. Cancellous bone – readily infiltrated
resorbed by tumor
5. Dense cortical bone - temporary barriers
 A safe margin of uninvolved bone is 2 cm for
solid and multicystic lesion
 1-1.5 for unicystic and peripheral lesions
 Resorption of cortical bone – periosteum
involved – surrounding soft tissue and muscle
 Post treatment follow up 15-20 yrs
Specific principles
Intra osseous solid / multi cystic
ameloblastoma
 Excision of lesion
 Enbloc resection -- without continuity
defect
 Enbloc resection– with continuity
defect
 Inferior alveolar nerve if in lesion- sacrificed
 Nerve grafting best to perform at time of
resection
 Resection should be exterior to tumor
involving plane
 A thin inferior border preserved may fracture-
reconstruction plate
 <1 cm not practical
 Resection with sharp cutting instrument
 Grinding with bur – not allow histologic
evaluation at tumor bone interface
Confirmed by frozen section
 Immediate reconstruction
Delayed reconstruction
• Autogenous free bone graft
• Allogenic bone with reconstruction plate
• Platelet rich plasma mixed into a cortical/
cancellous bone graft
• If sufficient soft tissue not available -
vascularized composite pedicle graft
• Delayed reconstruction : reconstruction plate to
maintain resection space
An anatomic classification of maxillary ameloblastoma as
an aid to surgical treatment
I T Jackson and P P Callan
J Cranio Maxillofac Surg 1996;24; 230
Group I tumors confined to maxilla with out involving orbital floor
- Partial maxillectomy
Group II tumor involving orbital floor not the periorbital tissue
- total maxillectomy
Group III tumor involving orbital contents
- total maxillectomy with orbital excentration
Group IV tumor involving skull base
- total maxillectomy with orbital excentration and anterior
skull base resection
Unicystic ameloblastoma
 Initial diagnosis
 Dentigerous cyst or OKC
 Enucleation or marsupialization?
 Careful assessment
 Biopsy may not confirm
 Physical basis cleavage plane
 Microscopic section R without CD or
R with CD
Peripheral ameloblastoma
 Enmass excision
 With overlying mucosa periosteum
alveolar bone and adjacent teeth
 1-1.5 resection margin
Cautery
 Chemical agents
 Electro cautery
 Cryotherapy
Carnoy’ solution
• Culter & Zollinger 1933 described as a
sclerozing agent for the treatment of cysts and
fistulae, and remains in use today as a fixative
Composition
i. Glacial acetic acid
ii. Absolute alcohol
iii. Chloroform
iv. Ferric chloride
• Depth of penetration 1.5-1.8 mm
Unicystic ameloblastoma – use of Carnoy’s
solution after enucleation
P K Lee N Samman
Int J Oral Maxillofac Surg 2004; 33 ; 263-7
Cryotherapy
 Adjunct to curettage
 Devitalize the tissue with liquid nitrogen
Depth 1.5 cm
 Jaw can be frozen the entire thickness
 Complication sequestration and pathologic
fracture
 Transient anesthesia
Management of mandibular ameloblastoma
treatment algorithm
Daniel E Sampson, M. Anthony Pogrel
J Oral Maxfac Surg 57; 1074-77 :1999
• Curettage recurrence
• Curettage with cryotherapy
• Confined to bone respond well to cryotherapy
• Soft tissue extension – necrosis
• Pathologic fracture – secondary to necrosis and
demineralization of bone
• Immediate bone grafting
Radiotherapy
 Inoperable cases
 Invasion into cranium
 Primarily intraosseous- resistant
 Extra osseous ameloblastoma - reduced
 Possible osteoradionecrosis
 Cause of metastasis
MALIGNANT BEHAVIOUR AND META STASIS
• Malignant ameloblastoma is a histologically well-
differentiated, benign appearing ameloblastoma with
metastatic disease histologically identical to the primary
tumor.
• Ameloblastic carcinoma is an ameloblastoma with
histological malignant transformation in the primary
lesion with or without metastatic disease.
• Metastases from malignant ameloblastomas have been
reported in the
– lung (75%),
– cervical lymph nodes (15%),
– spine (15%), and,
– less frequently, in the liver, skull, diaphragm, and brain.
• Markedly aggressive clinical course
• Quiescent chronicity
• After irradiation
Pulmonary metastasis of ameloblastoma
James M Henderson, J R Sonnet
J. Oral Surg Oral Path Oral Med Oral Radiol Endod;88 ;170-6:1999
• 41 cases metastatic to lung has been reported
• Inadequate and inappropriate treatment – recurrence
increased risk of metastasis
• Route aspiration of tumor particles/ hematogenous
spread
Rational approach to diagnosis and treatment of
ameloblastoma and OKC
Karen A O M Chapelle, Paul J W Stoclinge
British J Oral Maxfac Surg 42; 381-390 :2004
ameloblastoma
Ameloblastoma in children
R A Ord, R H Blanchaert Et Al
J Oral Maxfac Surg 60; 762-70 : 2002
 Differ
 Higher % unicystic and fast growing
 Mural invasion
 More aggressive surgery necessary
In discussion
Arie Shteyer suggest
1. Precise differential diagnosis
2. Conservative approach
 Decompression- Iodoform gauze
soaked in whiteheads varnish
3. Long term follow up
4. recurrence extensive surgery
Conclusion
• Careful examination
• Appropriate treatment
• Complete cure
• Reconstruction
• Follow up
THANK YOU

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AMELOBLASTOMA. (Dr MANOJ KUMAR)

  • 1.
  • 3. INTRODUCTION The permutation of different cells of different origin makes odontogenic tumors a highly complicated group of lesions
  • 4. EPITHELIAL ODONTOGENIC TUMORS 1. Minimal inductive change in CT  Ameloblastoma.  CEOT (Pindborg’s)  AOT 2. Extensive inductive changes in connective tissue  Ameloblastic fibroma  Ameloblastic fibro-odontoma  Odoto- Ameloblastoma  Odontoma – Complex Compound
  • 5. MESODERMAL ODONTOGENIC TUMOURS  Central odontogenic fibroma  Odontogenic myxoma  Cementoma – • Periapical cemental dysplasia • Cementifying fibroma • Benign cementoblastoma  Dentinoma
  • 6. Malignant odontogenic tumors – Odontogenic carcinoma • Primary intraosseous carcinoma • Malignant Ameloblastoma – Odontogenic Sarcoma • Ameloblastic Fibrosarcoma • Ameloblastic Odontosarcoma
  • 8. WHO (1992) “Is a true neoplasm of enamel organ like tissue which does not undergo differentiation to the point of enamel formation”
  • 9. Robinson described it as A tumour that is usually unicentric, nonfunctional intermittent in growth anatomically benign clinically persistent
  • 10. Synonyms :  Admantinoma  Multilocular cyst  Admantoblastoma  Eve’s Diesease
  • 11. History : • CUZACK (1827)- First Recognized • FALKSON (1879) – Description • MALASSEZ (1885) – Admantinoma • IVY &CHURCHILL (1934) – Ameloblastoma • Unicystic ameloblastoma – Robinson and Martinez in 1977
  • 12. ORIGIN • Cell rests of enamel organ – Dental lamina remnants – Hertwig’s sheath – Rests of malassez • Epithelium of Odontogenic cysts (Dentigerous cyst & Odontomas) • Disturbances in developing enamel organ. • Heterotropic epithelium in other parts of the body, especially the Pituitary Gland. • Basal cells of oral epithelium.
  • 13. extra osseous • Dental lamina ameloblast • Oral epithelium
  • 14. Incidence  1% of oral tumors  18-20% of odontogenic tumors
  • 15. Clinical features  20-50 years  Number of cases reported in children  Youngest reported one month old  Oldest 98 yrs
  • 16.  Frequent in mandible than maxilla  3:1
  • 17. Signs & symptoms  Asymptomatic  Asymmetry  Slow growing – non tender  Later stages pain
  • 18.  Secondary infection  Ulceration  Egg shell crackling  Extra osseous Small nodule
  • 19. Classification Robinson and Martinez 1977 Anatomic site 1. Central /intraosseous i. Multicystic/Conventional ii. Unicystic iii.solid 2. Peripheral/ extra osseous
  • 20. Radiological features • Numerous well defined radioluscency of varying diameter • Honey comb • Soap bubble appearance • Unicystic radiolucent lesion indistinguishable with cysts
  • 21.
  • 22.
  • 23. Ameloblastoma With in medullary cavity Scalloping of inner cortex Pressure erosion Shell remains
  • 24.
  • 26.
  • 27.  When maxillary sinus involved  Cloudiness of sinus  Destruction of wall  Unicystic in maxilla
  • 28. Histopathology • Follicular • Plexiform • Acanthomatous • Granular cell • Desmoplastic • Basal cell type
  • 35. Unicystic ameloblastoma Ackerman in 1988 1. Type-I Luminal (consisted of unilocular cystic lesions lined by epithelium exhibiting features of ameloblastoma). 1. Type-II Intra luminal (showed epithelial nodules arising from the cystic lining and projecting into the cyst lumen. These nodules comprised epithelium with a plexiform or follicular pattern resembling that seen in intraosseous ameloblastoma.). 1. Type-III Mural ameloblastoma (characterized by the presence of invasive islands of ameloblastomatous epithelium in the connective tissue wall of the cyst, and these islands may or may not be connected to the cyst lining)
  • 36.
  • 38.
  • 39. Peripheral ameloblastoma • Peripheral ameloblastoma (PA) is a rare odontogenic tumor that accounts for 1% for all ameloblastomas. • Kuri first reported PA in 1911 • In 1959, Stanley and Krogh defined the clinical and histopathologic characteristics. • The strict definition of PA according to Buchner and Scuibba (1987) excludes lesions in extragingival locations.
  • 40. The etiology of PA is unclear. The tumor can derive from the extraosseous epithelial remnants of the dental lamina or from the basal cell layer of the oral mucosa, which is believed to have odontogenic potential
  • 41. • The differential diagnosis usually includes – Pyogenic granuloma, peripheral – Giant cell granuloma, – Peripheral odontogenic fibroma, – Peripheral ossifying fibroma, – Papilloma, – Epulis. • Only four cases of malignant PA have been reported to date.
  • 43. DIFFERENTIAL DIAGNOSIS –Multilocular cyst Dentigerous cyst Odontogenic kerato cyst –Giant cell granuloma, cherubism –Brown’s tumor –Central hemangioma –Odontogenic myxoma
  • 44. Treatment –Behavior and potential of tumor –Growth characteristics –Anatomic site –Clinical extent –Size of tumor –Histologic pattern
  • 45.
  • 46. Less than complete excision is equivalent to planned recurrence
  • 48. 1. Definitive & offer best cure 2. Curettage and enucleation – recurrence 3. Curettage condemned 4. Cancellous bone – readily infiltrated resorbed by tumor 5. Dense cortical bone - temporary barriers
  • 49.  A safe margin of uninvolved bone is 2 cm for solid and multicystic lesion  1-1.5 for unicystic and peripheral lesions  Resorption of cortical bone – periosteum involved – surrounding soft tissue and muscle  Post treatment follow up 15-20 yrs
  • 51. Intra osseous solid / multi cystic ameloblastoma  Excision of lesion  Enbloc resection -- without continuity defect  Enbloc resection– with continuity defect
  • 52.
  • 53.
  • 54.  Inferior alveolar nerve if in lesion- sacrificed  Nerve grafting best to perform at time of resection  Resection should be exterior to tumor involving plane
  • 55.  A thin inferior border preserved may fracture- reconstruction plate  <1 cm not practical  Resection with sharp cutting instrument  Grinding with bur – not allow histologic evaluation at tumor bone interface
  • 56. Confirmed by frozen section  Immediate reconstruction Delayed reconstruction
  • 57. • Autogenous free bone graft • Allogenic bone with reconstruction plate • Platelet rich plasma mixed into a cortical/ cancellous bone graft • If sufficient soft tissue not available - vascularized composite pedicle graft • Delayed reconstruction : reconstruction plate to maintain resection space
  • 58. An anatomic classification of maxillary ameloblastoma as an aid to surgical treatment I T Jackson and P P Callan J Cranio Maxillofac Surg 1996;24; 230 Group I tumors confined to maxilla with out involving orbital floor - Partial maxillectomy Group II tumor involving orbital floor not the periorbital tissue - total maxillectomy Group III tumor involving orbital contents - total maxillectomy with orbital excentration Group IV tumor involving skull base - total maxillectomy with orbital excentration and anterior skull base resection
  • 59. Unicystic ameloblastoma  Initial diagnosis  Dentigerous cyst or OKC  Enucleation or marsupialization?  Careful assessment  Biopsy may not confirm  Physical basis cleavage plane  Microscopic section R without CD or R with CD
  • 60. Peripheral ameloblastoma  Enmass excision  With overlying mucosa periosteum alveolar bone and adjacent teeth  1-1.5 resection margin
  • 61. Cautery  Chemical agents  Electro cautery  Cryotherapy
  • 62. Carnoy’ solution • Culter & Zollinger 1933 described as a sclerozing agent for the treatment of cysts and fistulae, and remains in use today as a fixative Composition i. Glacial acetic acid ii. Absolute alcohol iii. Chloroform iv. Ferric chloride • Depth of penetration 1.5-1.8 mm
  • 63. Unicystic ameloblastoma – use of Carnoy’s solution after enucleation P K Lee N Samman Int J Oral Maxillofac Surg 2004; 33 ; 263-7
  • 64. Cryotherapy  Adjunct to curettage  Devitalize the tissue with liquid nitrogen Depth 1.5 cm  Jaw can be frozen the entire thickness  Complication sequestration and pathologic fracture  Transient anesthesia
  • 65. Management of mandibular ameloblastoma treatment algorithm Daniel E Sampson, M. Anthony Pogrel J Oral Maxfac Surg 57; 1074-77 :1999 • Curettage recurrence • Curettage with cryotherapy • Confined to bone respond well to cryotherapy • Soft tissue extension – necrosis • Pathologic fracture – secondary to necrosis and demineralization of bone • Immediate bone grafting
  • 66. Radiotherapy  Inoperable cases  Invasion into cranium  Primarily intraosseous- resistant  Extra osseous ameloblastoma - reduced  Possible osteoradionecrosis  Cause of metastasis
  • 67. MALIGNANT BEHAVIOUR AND META STASIS • Malignant ameloblastoma is a histologically well- differentiated, benign appearing ameloblastoma with metastatic disease histologically identical to the primary tumor. • Ameloblastic carcinoma is an ameloblastoma with histological malignant transformation in the primary lesion with or without metastatic disease.
  • 68. • Metastases from malignant ameloblastomas have been reported in the – lung (75%), – cervical lymph nodes (15%), – spine (15%), and, – less frequently, in the liver, skull, diaphragm, and brain. • Markedly aggressive clinical course • Quiescent chronicity • After irradiation
  • 69. Pulmonary metastasis of ameloblastoma James M Henderson, J R Sonnet J. Oral Surg Oral Path Oral Med Oral Radiol Endod;88 ;170-6:1999 • 41 cases metastatic to lung has been reported • Inadequate and inappropriate treatment – recurrence increased risk of metastasis • Route aspiration of tumor particles/ hematogenous spread
  • 70. Rational approach to diagnosis and treatment of ameloblastoma and OKC Karen A O M Chapelle, Paul J W Stoclinge British J Oral Maxfac Surg 42; 381-390 :2004
  • 72. Ameloblastoma in children R A Ord, R H Blanchaert Et Al J Oral Maxfac Surg 60; 762-70 : 2002  Differ  Higher % unicystic and fast growing  Mural invasion  More aggressive surgery necessary
  • 73. In discussion Arie Shteyer suggest 1. Precise differential diagnosis 2. Conservative approach  Decompression- Iodoform gauze soaked in whiteheads varnish 3. Long term follow up 4. recurrence extensive surgery
  • 74. Conclusion • Careful examination • Appropriate treatment • Complete cure • Reconstruction • Follow up