Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Dentin dysplasia (DD) is a rare hereditary disturbance is inherited as an autosomal dominant trait.
unknown etiology that affects approximately 1 :100,000.
In 1972, Witkop classified it into type I and type II which affect both dentitions.DD Type I
Radicular dentin dysplasia
Characterized by:-
1.Both dentitions are affected.
2.Normal appearing crowns
3.No or only rudimentary root development (rootless teeth)
4.Incomplete or total obliteration of the pulp chamber.
5.Teeth may exhibit extreme mobility and exfoliate prematurely.DD type II
coronal dentin dysplasia
Characterized by:-
1.partial pulpal obliteration.
2.Thistle-tube-or flame-shaped coronal pulp chambers
3. Thread-like root canals
4. Usually the absence of periapical radiolucencies.
5. In this type of anomaly, teeth roots are of normal shape and contour.The enamel and the immediately subjacent dentin appear normal.
Deeper layers of dentin show an atypical tubular pattern with an amorphous, atubular area, and irregular organization.
Normal dentinal tubule formation appears to have been blocked so that new dentine forms around obstacles and takes on the characteristic appearances described as “lava flowing around boulders”The radiograph revealed features of dentine dysplasia type I with normal appearance of crown but no root development Autosomal Dominant Disorder:
Manifested in heterozygous states
At least one parent of index case is usually affected
Both males and females are affected.
Clinical feature can be modified by variation in penetrance and expressivity. Some individual inherit the mutant gene but are phenotpically normal. This is reffered to as “incomplete penetrance”.
In many condition the age of onset is delayed.
Inheritance Pattern:
Typical pattern is a heterozygous affected parent with a homozygous unaffected parent.
Every child has one chance in two of having the disease
Both sexes are affected equally..Autosomal Recessive Disorder
Largest category of Mendelian disorder
Usually does not affect the parent of the affected individual, but sibling may show the disease.
Complete penetrance is common.
Onset is frequently early in life.
Usually affect enzymatic proteins.
Pattern Of Inheritance:
Typical pattern is two heterozygous unaffected (carrier) parent.
The triat does not usually affect the parent, but siblings may show the disease
Siblings have one chance in four of being affected
Both sexes affected equally.
An overview of various pathological processes affecting the Jaw Bones- Maxilla and Mandible including odontogenic cysts and tumours including their radiological findings!
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.
A cyst is an epithelium-lined sac containing fluid or semisolid material. In the formation of a cyst, the epithelial cells first proliferate and later undergo degeneration and liquefaction. The liquefied material exerts equal pressure on the walls of the cyst from within. Cysts grow by expansion and thus displace the adjacent teeth by pressure. May can produce expansion of the cortical bone. On a radiograph, the radiolucency of a cyst is usually bordered by a radiopaque periphery of dense sclerotic bone. The radiolucency may be unilocular or multilocular. Odontogenic cysts are those which arise from the epithelium associated with the development of teeth. The source of epithelium is from the enamel organ, the reduced enamel epithelium, the cell rests of Malassez or the remnants of the dental lamina.
Dentin dysplasia (DD) is a rare hereditary disturbance is inherited as an autosomal dominant trait.
unknown etiology that affects approximately 1 :100,000.
In 1972, Witkop classified it into type I and type II which affect both dentitions.DD Type I
Radicular dentin dysplasia
Characterized by:-
1.Both dentitions are affected.
2.Normal appearing crowns
3.No or only rudimentary root development (rootless teeth)
4.Incomplete or total obliteration of the pulp chamber.
5.Teeth may exhibit extreme mobility and exfoliate prematurely.DD type II
coronal dentin dysplasia
Characterized by:-
1.partial pulpal obliteration.
2.Thistle-tube-or flame-shaped coronal pulp chambers
3. Thread-like root canals
4. Usually the absence of periapical radiolucencies.
5. In this type of anomaly, teeth roots are of normal shape and contour.The enamel and the immediately subjacent dentin appear normal.
Deeper layers of dentin show an atypical tubular pattern with an amorphous, atubular area, and irregular organization.
Normal dentinal tubule formation appears to have been blocked so that new dentine forms around obstacles and takes on the characteristic appearances described as “lava flowing around boulders”The radiograph revealed features of dentine dysplasia type I with normal appearance of crown but no root development Autosomal Dominant Disorder:
Manifested in heterozygous states
At least one parent of index case is usually affected
Both males and females are affected.
Clinical feature can be modified by variation in penetrance and expressivity. Some individual inherit the mutant gene but are phenotpically normal. This is reffered to as “incomplete penetrance”.
In many condition the age of onset is delayed.
Inheritance Pattern:
Typical pattern is a heterozygous affected parent with a homozygous unaffected parent.
Every child has one chance in two of having the disease
Both sexes are affected equally..Autosomal Recessive Disorder
Largest category of Mendelian disorder
Usually does not affect the parent of the affected individual, but sibling may show the disease.
Complete penetrance is common.
Onset is frequently early in life.
Usually affect enzymatic proteins.
Pattern Of Inheritance:
Typical pattern is two heterozygous unaffected (carrier) parent.
The triat does not usually affect the parent, but siblings may show the disease
Siblings have one chance in four of being affected
Both sexes affected equally.
An overview of various pathological processes affecting the Jaw Bones- Maxilla and Mandible including odontogenic cysts and tumours including their radiological findings!
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.
A cyst is an epithelium-lined sac containing fluid or semisolid material. In the formation of a cyst, the epithelial cells first proliferate and later undergo degeneration and liquefaction. The liquefied material exerts equal pressure on the walls of the cyst from within. Cysts grow by expansion and thus displace the adjacent teeth by pressure. May can produce expansion of the cortical bone. On a radiograph, the radiolucency of a cyst is usually bordered by a radiopaque periphery of dense sclerotic bone. The radiolucency may be unilocular or multilocular. Odontogenic cysts are those which arise from the epithelium associated with the development of teeth. The source of epithelium is from the enamel organ, the reduced enamel epithelium, the cell rests of Malassez or the remnants of the dental lamina.
Odontogenic tumors are growths that develop in the jawbones or soft tissues of the mouth, arising from the tissues that form teeth. These tumors can be benign or malignant and vary widely in their presentation and behavior. Benign tumors include ameloblastoma, odontoma, and cementoblastoma, while malignant tumors include ameloblastic carcinoma and odontogenic sarcoma. Treatment typically involves surgical removal, and prognosis depends on the type and stage of the tumor.
Odontogenic tumors iii/certified fixed orthodontic courses by Indian dental a...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
Cysts &tumors of salivary glands /certified fixed orthodontic courses by Indi...Indian dental academy
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Indian dental academy provides dental crown & Bridge,rotary endodontics,fixed orthodontics,
Dental implants courses.for details pls visit www.indiandentalacademy.com ,or call
0091-9248678078
Odontogenic tumors iv /orthodontic courses by Indian dental academy Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
A lecture for 5th stage dental students.
any questions or notes please contact me on theses links :
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New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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
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.
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
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
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