benign tumours of salivary glands
TRANSCRIPT
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MAHAK RALLI, ROLL NO. 42
BENIGN TUMOURS OF SALIVARY GLANDS
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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 )
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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.
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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 massRarely ulcerates the overlying skinIn 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.
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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.
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Typical appearance of pleomorphic adenoma
Removal of palatal tumour
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PATHOLOGY
• Gross appearance Firm, smooth mass within a pseudocapsule• Histological appearanceHas both epithelial and mesenchymal cellsStroma consists of chondroid, myxoid, osseous and
fibroid cellsThere is presence of microscopic projections which
are necessary to remove, or they become the cause for recurrence.
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Neoplastic cells are seen arranged in ductal patterns, sheets and islands. Stroma is delicately collagenous with myxoid areas.
Few cells show vacoular degenartion
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Neoplastic cells are seen arranged in ductal patterns, sheets and islands. Stroma is delicately collagenous with myxoid areas.
Few cells show vacoular degenartion
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DIFFERENTIAL DIAGNOSIS AND TREATMENT
• DIFFERENTIAL DIAGNOSISAdenolymphomaOncocytomaAdenocarcinoma 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
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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.
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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 massIt is firm in consistency or fluctuantIt 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.
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CLINICAL APPEARANCE
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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.
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DIFFERENTIAL DIAGNOSIS AND TREATMENT
• DIFFERENTIAL DIAGNOSISPleomorphic adenomaOncocytomaParotid lymph node enlargement
• TREATMENTSurgical excision involving a margin of normal tissueIn cases where a significant amount of superficial
lobe is affected, superficial parotidectomy is done.Recurrence and malignant changes are rare
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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.
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CLINICAL FEATURES
• Age- 50 to 80 years• Gender- female predilection• Location- parotid gland most commonly affected• Signs and symptoms- Discrete, encapsulated, slow growing mass3-5cm in diameterPainless and firmDiffuse multinodular oncocytoma appears when
many nodular masses involve the entire glandCan occur bilaterallyRarely seen intraorally
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Oncocytoma, clinical appearance
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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 scintigraphyMalignant oncocytomas can occur and are
aggressive.
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DIFFERENTIAL DIAGNOSIS AND TREATMENT
• DIFFERENTIAL DIAGNOSISPleomorphic adenomaWarthins tumourParotid lymphnode enlargement• TREATMENTSuperficial parotidectomy with preservation of the
facial nerve, in parotid glandRemoval of the gland, in submandibular glandGland removal with a normal cuff of tissue is the
treatment of choice for oncocytomas of minor salivary glands
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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
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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 movablePainlessLess than 3cm in diameter
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CLINICAL APPEARANCE
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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 epithelium3.Membranous form- multilocular and 50% cases are
encapsulated. It grows in clusters interspersed with normal salivary gland tissue.
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DIFFERENTIAL DIAGNOSIS AND TREATMENT
• DIFFERENTIAL DIAGNOSISCanalicular adenomaSebaceous adenomaClear cell adenoma• TREATMENTConservative surgical excision extending to normal
tissue. Low recurrence rate, except membranous form
maybe.
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CANALICULAR ADENOMA
• Uncommon neoplasm composed of epithelial cells arranged in a single or double layer forming branching cords in a loose stroma• CLINICAL FEATURESAge- older than 50 yearsGender- female predilectionLocation- 80% cases in the upper lipSymptoms and signs- slow growing, movable and
asymptomatic. Well-circumscribed and painless.
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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.
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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.
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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.
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TREATMENT
• Standard surgical excision, including a border of normal tissue, is recommended.• Recurrence is uncommon.
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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 PRESENTATIONEncapsulated or sharply circumscribed tumour that
varies in color from grayish white to pinkish white to yellow or yellowish grey.
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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.• TREATMENTConservative excision.No recurrences.
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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 projections2.All three tumours arise from the excretory duct3.Commonly affects the minor salivary gland• Three benign tumours include-1.Intraductal papilloma2.Sialadenoma papilliferum3.Inverted ductal papilloma
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SIALADENOMA PAPILLOMA
• CLINICAL FEATURESAge- 30 to 70 yearsMale predilectionMost commonly seen on palate and buccal
mucosa minor glands.Well-circumscribed, painless, papillary exophytic
growth
• HISTOLOGYEpithelium lined papillary projections supported by
fibrovascular connective tissue, forming a series of clefts within the lesion
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INVERTED DUCTAL PAPILLOMA
• CLINICAL FEATURESAge- 30 to 60 years.Male predilectionBuccal mucosa, lower lip and vestibule of lower
jaw.Asymptomatic, firm, submucosal nodule <1.5cmOccurs near the orifice of salivary gland ducts.• HISTOLOGY• Resembles sialadenoma• Consists of projections of ductal epithelium that
proliferate to surrounding tissues, forming clefts.
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TREATMENT
• Surgical excision• Recurrence is rare.
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