This document provides information on various benign tumours of the salivary glands, including pleomorphic adenoma, Warthin's tumour, oncocytoma, basal cell adenoma, canalicular adenoma, myoepithelioma, sebaceous adenoma, and ductal papillomas. It describes the location, histology, clinical features, differential diagnosis, and treatment for each tumour type. The most common benign salivary gland tumour is the pleomorphic adenoma, which can occur in the parotid, submandibular, and minor salivary glands. Surgical excision is typically the treatment.
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
Juvenile Ossifying Fibroma
Two patterns
Trabecular
Psammomatoid,
Trabecular form
Seen in younger patients.
Mean age is approximately 11 years,
Psammomatoid form
Appears outside of the jaws
70% arising in the orbital and frontal bones and paranasal sinuses.
Clinical Features
Early to late childhood
Maxilla > Mandible
Singular, slow-growing, painless swelling
Overgrowth of tissue that occurs centrally in the jaws
May involve impacted or unerupted teeth disfiguring
Increased level of serum alkaline phosphatase
Severe maloccusion
Aggressive form:
Symptomatic if traumatized
Ulcerated
Maxilla lesion may interfere with sight and breathingHistologic Features:
Psammomatoid form
Abundant cellular fibrous connective tissue in a whorled pattern
Proliferating fibroblasts form spicules of bone and
Cementum at maturity the bone may be somewhat normal,
Areas of hemorrhage and small clusters of multinucleated giant cells,
Trabecular variant
shows irregular strands of highly cellular osteoid encasing plump and irregular osteocytes.
The psammomatoid pattern forms concentric lamellated and spherical ossicles that vary in shape and typically have basophilic centers with peripheral eosinophilic osteoid rims
Radiographic Features: Radiolucent or mixed radiolucent and radiopaque appearance (ground glass),
Lamina dura is usually obscured and the cortical plates thinned
Treatment and Prognosis:Management and prognosis are uncertain.
Smaller lesions, complete local excision or thorough curettage appears adequate,
Rapidly growing lesions, wider resection may be required
Recurrence rates of 30% to 58%
Malignant transformation has not been documented.
An overview of various pathological processes affecting the Jaw Bones- Maxilla and Mandible including odontogenic cysts and tumours including their radiological findings!
Ghost cells are translucent balloon shaped , elliptical epithelial cells are recognized as swollen, pale, eosinophilic cells.
They are seen either singly or in sheets with a clear conservation of basic cellular outline, generally with apparent clear areas or with some remnants indicative of the site previously occupied by the nucleus.
The transformation of epithelial cells into more resistant terminally differentiated apoptotic cells i.e., ghost cells are responsible for the banal behavior of neoplasms and they also help in relieving the stress of the forming neoplasm.
The most accepted nature of ghost cells is aberrant keratinization that is altered form of keratin as it doesn’t stain with normal cytokeratin antibodies.
Tonofilaments have been observed universally in the ghost cells of all the odontogenic or non-odontogenic tumors but these solely don’t satisfy their nature which is also found to be positive for enamel proteins in odontogenic tumors.
Although, studies prove an intricate functional relationship exists between Wnt and Notch signalling during development of neoplasms and in assigning cells to particular fates.
Their relationship along with other signalling pathways complex interaction during tumorigenesis also needs intensive evaluation and this would help revealing the missing link between odontogenic and non-odontogenic tumors exhibiting these similar looking mysterious ghost cells.
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.
Juvenile Ossifying Fibroma
Two patterns
Trabecular
Psammomatoid,
Trabecular form
Seen in younger patients.
Mean age is approximately 11 years,
Psammomatoid form
Appears outside of the jaws
70% arising in the orbital and frontal bones and paranasal sinuses.
Clinical Features
Early to late childhood
Maxilla > Mandible
Singular, slow-growing, painless swelling
Overgrowth of tissue that occurs centrally in the jaws
May involve impacted or unerupted teeth disfiguring
Increased level of serum alkaline phosphatase
Severe maloccusion
Aggressive form:
Symptomatic if traumatized
Ulcerated
Maxilla lesion may interfere with sight and breathingHistologic Features:
Psammomatoid form
Abundant cellular fibrous connective tissue in a whorled pattern
Proliferating fibroblasts form spicules of bone and
Cementum at maturity the bone may be somewhat normal,
Areas of hemorrhage and small clusters of multinucleated giant cells,
Trabecular variant
shows irregular strands of highly cellular osteoid encasing plump and irregular osteocytes.
The psammomatoid pattern forms concentric lamellated and spherical ossicles that vary in shape and typically have basophilic centers with peripheral eosinophilic osteoid rims
Radiographic Features: Radiolucent or mixed radiolucent and radiopaque appearance (ground glass),
Lamina dura is usually obscured and the cortical plates thinned
Treatment and Prognosis:Management and prognosis are uncertain.
Smaller lesions, complete local excision or thorough curettage appears adequate,
Rapidly growing lesions, wider resection may be required
Recurrence rates of 30% to 58%
Malignant transformation has not been documented.
An overview of various pathological processes affecting the Jaw Bones- Maxilla and Mandible including odontogenic cysts and tumours including their radiological findings!
Ghost cells are translucent balloon shaped , elliptical epithelial cells are recognized as swollen, pale, eosinophilic cells.
They are seen either singly or in sheets with a clear conservation of basic cellular outline, generally with apparent clear areas or with some remnants indicative of the site previously occupied by the nucleus.
The transformation of epithelial cells into more resistant terminally differentiated apoptotic cells i.e., ghost cells are responsible for the banal behavior of neoplasms and they also help in relieving the stress of the forming neoplasm.
The most accepted nature of ghost cells is aberrant keratinization that is altered form of keratin as it doesn’t stain with normal cytokeratin antibodies.
Tonofilaments have been observed universally in the ghost cells of all the odontogenic or non-odontogenic tumors but these solely don’t satisfy their nature which is also found to be positive for enamel proteins in odontogenic tumors.
Although, studies prove an intricate functional relationship exists between Wnt and Notch signalling during development of neoplasms and in assigning cells to particular fates.
Their relationship along with other signalling pathways complex interaction during tumorigenesis also needs intensive evaluation and this would help revealing the missing link between odontogenic and non-odontogenic tumors exhibiting these similar looking mysterious ghost cells.
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.
Presentation about the the second most common type of ovarian tumors which have a very unique property of being similar to the testicular germ cell tumors.
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Endometrial Ca classification and histopathological features , CAP protocol for reporting , grading and staging tumors
Reference - Robbins , Rosai & Ackerman , Sternberg ,Fletcher ,WHO classification of tumors of female reproductive system, CAP
How to Make a Field invisible in Odoo 17Celine George
It is possible to hide or invisible some fields in odoo. Commonly using “invisible” attribute in the field definition to invisible the fields. This slide will show how to make a field invisible in odoo 17.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
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Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
Introduction to AI for Nonprofits with Tapp NetworkTechSoup
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June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
unwillingness to rectify this violation through action requires accountability.
Postsecondary education is a unique opportunity for students to learn and have their ideas and beliefs challenged. However, universities receiving hundreds of millions of federal funds annually have denied
students that opportunity and have been hijacked to become venues for the promotion of terrorism, antisemitic harassment and intimidation, unlawful encampments, and in some cases, assaults and riots.
The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
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2. PLEOMORPHIC ADENOMA
• Most common benign salivary neoplasm consisting
of cells exhibiting the ability to differentiate
epithelial cells (ductal and nonductal cells)
mesenchyme-like cells (chondroid, myxoid or
osseous)
• This results in different histopathologic patterns in the
tumours. Hence the name pleo- (meaning many)
morphic (meaning shape, form )
3. ETIOLOGY
• 60% of all salivary gland tumours
• 85% of these are found in the parotid gland, 8% in
submandibular gland and the remaining in
sublingual and minor salivary glands
• Histogenesis –
Numerous theories have been advanced.
Current theory- based on myoepithelial and reverse
cells of the intercalated ducts.
4. CLINICAL FEATURES
• Age- 30 to 50 years
• Gender- slight female predilection
• Location –superficial lobe of parotid > submandiblar
gland> palate
• Signs and symptoms
It is a slow growing and painless mass
Rarely ulcerates the overlying skin
In parotid gland, the tumour grows in posterior and
inferior aspect of superficial lobe measuring a few
cms.
In the submandibular gland, it is a well defined
palpable mass.
5. CLINICAL FEATURES
• When occuring in the parotid, the ear lobe of the
affected side might elevate.
• When observed in-situ, it is encased in
pseudocapsule and exhibits a lobulated surface.
• The palatal tumours are smooth-surfaced and
dome shaped masses.
7. PATHOLOGY
• Gross appearance
Firm, smooth mass within a pseudocapsule
• Histological appearance
Has both epithelial and mesenchymal cells
Stroma consists of chondroid, myxoid, osseous and
fibroid cells
There is presence of microscopic projections which
are necessary to remove, or they become the
cause for recurrence.
8. Neoplastic cells are seen arranged in ductal patterns, sheets and islands.
Stroma is delicately collagenous with myxoid areas.
Few cells show vacoular degenartion
9. Neoplastic cells are seen arranged in ductal patterns, sheets and islands.
Stroma is delicately collagenous with myxoid areas.
Few cells show vacoular degenartion
10. DIFFERENTIAL DIAGNOSIS AND
TREATMENT
• DIFFERENTIAL DIAGNOSIS
Adenolymphoma
Oncocytoma
Adenocarcinoma
Warthin’s tumour
• TREATMENT
Surgical removal of the tumour including adequate
margin
Superficial parotidectomy, if the tumour is affecting
the parotid gland
Removal of the entire submandibular gland may be
required if the submandibuar gland is affected
11. PAPILLARY CYSTADENOMA
LYMPHOMATOSUM
• Also known as Warthin’s tumour.
• Second most common benign tumour seen in the
parotid gland
• It is characterized by proliferation of both luminal
and non-luminal cells.
12. CLINICAL FEATURES
• Age- 60 to 70 years
• Gender- slight male predilection
• Location- parotid most commonly affected, inferior
and posterior to the angle of mandible
• Signs and symptoms-
It is a slow growing, painless nodular mass
It is firm in consistency or fluctuant
It can occur as a bilateral lesion (unique feature)
It is metachronous i.e appearing at different times,
not simultaneously.
Oncocytes take up technetium and is visible on Tc
99m scintiscans.
15. PATHOLOGY
• Gross appearance-
Tumour is smooth and has a well defined capsule.
Cut specimen shows cystic spaces filled with thick
mucinous material.
• Histological appearance-
Cyst formation with papillary projections in the cystic
spaces.
Inner luminal cells are tall, columnar and eoisnophilic
with palisaded nuclei.
Outer luminal cells are cuboidal or polygonal.
There is characteristic lymphocytic infililtration.
16.
17.
18. DIFFERENTIAL DIAGNOSIS AND
TREATMENT
• DIFFERENTIAL DIAGNOSIS
Pleomorphic adenoma
Oncocytoma
Parotid lymph node enlargement
• TREATMENT
Surgical excision involving a margin of normal tissue
In cases where a significant amount of superficial
lobe is affected, superficial parotidectomy is done.
Recurrence and malignant changes are rare
19. ONCOCYTOMA
• Less common benign tumour (<1%)
• The name is derived from presence of oncocytes.
• These cells resemble the apparently normal cells.
• Oncocytic cells are considered as somatic mutants
rather than new specific cell lineage.
• Oncocytic transformation of epithelial cells is not
degenerative but rather a redifferentiation of
epithelial cells which develope an increased but
unbalanced metabolism.
20. CLINICAL FEATURES
• Age- 50 to 80 years
• Gender- female predilection
• Location- parotid gland most commonly affected
• Signs and symptoms-
Discrete, encapsulated, slow growing mass
3-5cm in diameter
Painless and firm
Diffuse multinodular oncocytoma appears when
many nodular masses involve the entire gland
Can occur bilaterally
Rarely seen intraorally
22. PATHOLOGY
• Gross appearance-
Non cystic and firm
• Histology-
Brown, granular eosinophilic cells with central nuclei
and arranged in sheets, nests or cord.
Oncocytes concentrate technetium and can be
visualized by Tc 99m scintigraphy
Malignant oncocytomas can occur and are
aggressive.
23.
24. DIFFERENTIAL DIAGNOSIS AND
TREATMENT
• DIFFERENTIAL DIAGNOSIS
Pleomorphic adenoma
Warthins tumour
Parotid lymphnode enlargement
• TREATMENT
Superficial parotidectomy with preservation of the
facial nerve, in parotid gland
Removal of the gland, in submandibular gland
Gland removal with a normal cuff of tissue is the
treatment of choice for oncocytomas of minor
salivary glands
25. BASAL CELL ADENOMA
• It is an uncommon salivary gland tumour,
histopathologically composed of basaloid
(resembling basal cells), epithelial cells arranged in
solid, trabecular, tubular or membranous patterns.
• Hence the name basal cell adenoma
• It arises from the neoplastic transformation of
reserve cells in intercalated ducts and shows
differentiation of both epithelial and myoepithelial
elements
26. CLINICAL FEATURES
• Age- 50 to 70 years
• Gender- female predilection
• Location- 70% in parotid, upper lip (minor salivary
gland)
• Signs and symptoms-
Slow growing, freely movable
Painless
Less than 3cm in diameter
28. PATHOLOGY
• It is well-encapsulated tumour in major salivary
glands whereas in minor salivary glands, the
capsule will be ill-defined
• Three varieties exist-
1.Solid- islands or sheets of basaloid cells. Normal
sized- nuclei and basophilic with minimal cytoplasm.
2.Trabecular-tubular form- cord of epithelium
3.Membranous form- multilocular and 50% cases are
encapsulated. It grows in clusters interspersed with
normal salivary gland tissue.
29.
30.
31. DIFFERENTIAL DIAGNOSIS AND
TREATMENT
• DIFFERENTIAL DIAGNOSIS
Canalicular adenoma
Sebaceous adenoma
Clear cell adenoma
• TREATMENT
Conservative surgical excision extending to normal
tissue.
Low recurrence rate, except membranous form
maybe.
32. CANALICULAR ADENOMA
• Uncommon neoplasm composed of epithelial cells
arranged in a single or double layer forming
branching cords in a loose stroma
• CLINICAL FEATURES
Age- older than 50 years
Gender- female predilection
Location- 80% cases in the upper lip
Symptoms and signs- slow growing, movable and
asymptomatic. Well-circumscribed and painless.
33. HISTOLOGY
• Long columns or cords of cuboidal columnar cells in
a single layer
• These layers are parallel, form long canals
• Sometimes, row of cells are loosely approximated
and appear as a double row of cells
• The supporting stroma is loose, fibrillar and highly
vascular.
• The cystic spaces are filled with eosinoplhilic
material.
34.
35. MYOEPITHELIOMA
• Uncommon salivary gland tumour (<1%)
• Occurs in the parotid gland and in minor salivary
glands of the palate.
• No gender predilection.
• Average age group affected is in the sixth decade
of life.
• Clinically, it is a well-circumscribed, asymptomatic,
slow-growing mass.
36. PATHOLOGY
• Consists of spindle-shaped, plasmacytoid cells, or a
combination of the two
• Diagnosis is based on identification of myoepithelial
cells and must be differentiated from other benign
and malignant epithelial and mesenchymal
tumours for treatment planning.
• Growth patterns vary from solid to a loose stroma
formation with myoepithelial cells.
• This tumour is epithelial in origin however, it
functionally resembles smooth muscle and is
demonstrated by immunohistochemical staining for
actin cytokeratin and S-100 protein.
37.
38.
39. TREATMENT
• Standard surgical excision, including a border of
normal tissue, is recommended.
• Recurrence is uncommon.
40. SEBACEOUS ADENOMA
• A rare benign tumour derived from sebaceous
glands located within salivary gland tissue
• Parotid gland is most commonly involved
• Age group affected – 22 to 90 years, mean age at
initial clinical presentation is 58 years.
• The tumour is more common in men.
• CLINICAL PRESENTATION
Encapsulated or sharply circumscribed tumour that
varies in color from grayish white to pinkish white to
yellow or yellowish grey.
41. PATHOLOGHY AND TREATMENT
• PATHOLOGY
• These are composed of sebaceous cell nests with
minimal atypia and pleomorphism and no
tendency to invade
• Sebaceous glands vary in size and are usually
embedded in a fibrous stroma.
• TREATMENT
Conservative excision.
No recurrences.
42. DUCTAL PAPILLOMA
• They include three rare benign salivary gland
neoplasms which exhibit papillary projections i.e.
showing surface projections, histologically.
• The unique features of this tumour are-
1.Papillar projections
2.All three tumours arise from the excretory duct
3.Commonly affects the minor salivary gland
• Three benign tumours include-
1.Intraductal papilloma
2.Sialadenoma papilliferum
3.Inverted ductal papilloma
43. SIALADENOMA PAPILLOMA
• CLINICAL FEATURES
Age- 30 to 70 years
Male predilection
Most commonly seen on palate and buccal
mucosa minor glands.
Well-circumscribed, painless, papillary exophytic
growth
• HISTOLOGY
Epithelium lined papillary projections supported by
fibrovascular connective tissue, forming a series of
clefts within the lesion
44. INVERTED DUCTAL PAPILLOMA
• CLINICAL FEATURES
Age- 30 to 60 years.
Male predilection
Buccal mucosa, lower lip and vestibule of lower
jaw.
Asymptomatic, firm, submucosal nodule <1.5cm
Occurs near the orifice of salivary gland ducts.
• HISTOLOGY
• Resembles sialadenoma
• Consists of projections of ductal epithelium that
proliferate to surrounding tissues, forming clefts.