Category Archives: Salivary Gland

Warthin’s Salivary Gland Tumor

Warthin’s Tumor

Clinical features

•    Second most common salivary gland neoplasm

•    Almost always arises in parotid gland

•    Occurs most commonly in males rather than females, usually in fifth to seventh decades of life

•    10% are multifocal; 10% are bilateral

•    Smokers are have an 8-fold risk than non-smokers for developing these tumours

Cytologic features on fine-needle aspiration

•    Mixed population of lymphocytes

•    Sheets of oncocytes

•    Granular background

Gross features

•    Round to oval encapsulated lesions

•    2-5 cm in diameter

•    Arise in superficial parotid gland where they are readily palpable

•    Sectioning reveals pale gray surface punctuated by narrow cystic or cleft-like spaces filled with a mucinous or serous secretion
Prognosis

•    Benign

•    Recurrence rate is only 2% after resection

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Salivary gland adenoid cystic carcinoma

Adenoid cystic carcinoma of the salivary gland

Frequency of adenoid cystic carcinoma in major and minor salivary glands

•    50% found in minor salivary glands (mainly palate)

•    Among major salivary glands, the parotid and submandibular gland are the most common locations

Histologic features

•    Composed of small cells with dark, compact nuclei and scant cytoplasm

•    Arranged in tubular, solid or cribriform patterns reminiscent of cylindromas of the skin

•    Spaces between tumor cells are filled with hyaline material thought to be excess basement membrane material

•    Presence of pseudoglandular lumina, true glandular lumina and perineural invasion is required for diagnosis

Differential diagnosis

•    Pleomorphic adenoma

•    Polymorphous low grade adenocarcinoma

Prognosis

•    Size

•    Location (minor salivary gland involvement is poor prognostic factor)

•    Stage (distant metastasis is poor prognosticator)

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Salivary Gland Metastases

Salivary Gland Metastases

Usually spreads to intraparotid node or submandibular lymph node and as it grows, mimics a primary neoplasm
Most common types are squamous cell carcinomas (from upper aerodigestive tract and skin) and malignant melanoma
Distant sites include  lung, kidney, breast are most common

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Salivary Gland

Salivary Gland

Normal salivary gland histology.

Salivary gland.

Salivary gland histology.

Salivary gland cells.

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Mucoepidermoid Carcinoma

Mucoepidermoid Carcinoma

Mucoepidermoid carcinoma.

Mucoepidermoid carcinoma of the salivary gland.

Salivary gland mucoepidermoid carcinoma.

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Adenoid Cystic Carcinoma

Adenoid Cystic Carcinoma

Gross

Small, poorly encapsulated, infiltrative, gray-pink

Histology

a.    Basaloid tumour, consisting of epithelial and myoepithelial cells
b.    Growth patterns – tubular, cribiform, solid
c.    Microcystic and pseudoglandular spaces filled with hyaline or basophilic mucoid material
d.    Perineural invasion is common

Clinical

a.    Slow growing mass, most frequently involving parotid, submandibular, minor salivary glands
b.    Pain with perineural invasion
c.    High rate of recurrence
d.    50% disseminate widely, sometimes decades after resection

Poor prognostic factors:

Minor salivary gland
Larger size
Facial nerve paralysis
Histologic pattern (solid)
Recurrence
Metastasis

Differential Diagnosis:

Basal cell adenoma/adenocarcinoma
Polymorphous low-grade adenoca
Pleomorphic adenoma

Treatment:

- radiosensitive; resection

Adenoid cystic carcinoma.

Carcinoma adenoid cystic.

Adnoid cystic cancer.

Salivary gland adenoid cystic carcinoma.

Adenoid cystic carcinoma of the salivary gland.

Adenoid cystic cells.

Adenoid cystic carcinoma cells.

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Myoepithelioma

Myoepithelioma

Myoepithelioma.

Salivary gland myoepithelioma.

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Pleomorphic Adenoma

Pleomorphic Adenoma

Pleomorphic Adenoma Gross Features

Round, well-demarcated, encapsulated (not always well-developed)
Expansile growth with tonguelike protrusions
Cut surface is gray-white with myxoid and blue translucent areas

- Well-defined ovoid tumours, encapsulated (except in minor glands)
Bossellated outer surface
-  Cut surface is homogeneous,  white or tan; glistening appearance where there are cartilaginous or  myxochondroid areas

Microscopic Features

Mixture of epithelial and myoepithelial cells
Myoepithelial cells are arranged in various patterns (tubules, strands, sheets…) and are dispersed within a loose myxoid background
May see islands of chondroid or bone
May see squamous metaplasia

Clinical:

Painless, slow-growing, mobile, discrete mass
Location: parotid, submandibular or buccal cavity
Incidence of malignant transformation increases with duration of tumour (2% for less than 5 yrs; 10% for more than 15 yrs)

Treatment:

Recurrence rate of 4% with adequate parotidectomy; 25% with enucleation
Pleomorphic Adenoma.

Pleomorphic Adenoma Histology.

Salivary gland pleomorphic adenoma.

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Oncocytoma

Oncocytoma

Oncocytoma.

Oncocytoma cells.

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Warthin’s Tumor

Warthin’s Tumor

Clinical Features

- M>F, 5th to 7th decade
- Strong association with smoking
- Almost exclusively parotid (superficial lobe, inferior pole)
- 10% multifocal, 10% bilateral

Cytologic features on FNA

- Sparsely cellular
- Sheets of oncocytes – orderly arrangement, no 3D crowding, no glandular formation or microacini
- Uniform, round, eccentric nuclei with even chromatin, indistinct nucleoli, granular cytoplasm
- May see mild atypia, prominent nucleoli – not sign of malignancy
- Degenerated oncocytes may be pyknotic with dense orangeophilic cytoplasm
- Mixed population of lymphocytes
- Granular background, may see atypical squamous metaplasia

Gross features

Round to oval, encapsulated mass 2-5 cm with a smooth or lobulated surface
Cut surface is pale gray
Cystic spaces (mucoid or brown exudates) with papillary projections from cysts
Solid white areas represent lymphoid follicles

Microscopic

Cystic spaces are lined by a double layer of cells, resting on a dense lymphoid stroma
The surface layer is oncocytic; the basal layer is cuboidal to polygonal
May see foci of squamous metaplasia

Prognosis

Benign; recurrence rate of 2% after resection
Transformation to malignancy is very rare and may include epithelial or lymphoid component
a.    Most common malignancies arising from Warthin’s are squamous cell carcinoma, lymphoma, mucoepidermoid carcinoma
Warthin's Tumor.

Warthin Tumor

Tumor Warthin's.

Salivary gland warthin's tumor.

Warthin's tumor cells.

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