Salivary Pathology Flashcards
Major salivary glands
Parotid glands, submandibular glands, sublingual gland
Minor salivary glands
- Palate (between midline and palatal gingiva)
- Lining mucosa (cheeks, vestibules, FOM, lips)
- Tongue (ventral & lateral surfaces)
The _____ nerve loops under the _____ duct.
lingual, submandibular
Gland with mostly serous acini
Parotid gland
Gland with mixed acini
Submandibular
Gland with purely mucous acini
Sublingual
_____ cells surround salivary acini and ducts
Myoepithelial
Non-infectious sialadenitis can be caused by
- Post-irradiation
- Immune mediated
- Sarcoidosis
Infectious sialadenitis can be
- Bacterial (acute, chronic, TB, Actinomycosis)
- Viral (mumps, cytomegalic inclusion disease, HIV)
Sialadenitis generally presents as
pain and swelling
Typically a retrograde infection, leading to progressive swelling of the gland 1-2 weeks + malaise, anorexia, dehydration +/- obstruction, fever & purulent exudate of stenson’s duct + pain exacerbated by eating or drinking
Acute bacterial parotitis
Predisposing factors of acute bacterial parotitis
Mouth dryness and/or dehydration, obstructed duct, poor oral hygiene, elderly pts
Acute bacterial parotitis appears microscopically as
sheets of neutrophils
Viral parotitis (Mumps) is a highly contagious viral disease caused by a member of
Paramyxovirus
Mumps is transmitted by
- direct contact, droplet spread
- Virus enter through nose/mouth and replicates in URT and LNs. Spreads to salivary glands and gonads, pancreas, meninges
Clinical symptoms of Mumps
Fever, malaise, headache/myalgia, painful swelling of parotids, submandibular, sublingual glands (pancreas, choroid plexus for the brain, ovaries, and testes in some cases)
Mumps breakouts occur in people living in
close quarters
Complications of Mumps
Deafness, pancreatitis, meningitis, inflammation of the testis and ovaries.
Children are vaccinated against mumps at what age with what vaccine?
1 y/o, MMR
Testing for Mumps
Clinical presentation, labs for Mumps specific IgM, IgG, or viral culture from parotid swab
Non-infectious sialadenitis includes
Immune-mediated sialadenitis (Sjogren syndrome), Sarcoidosis, Post-irradiation
Chronic swelling of the Parotid glands accompanied by dry mouth and eyes. More frequently accompanied by other autoimmune disease (RA, SLE)
Immune mediated sialadenitis (Sjogren syndrome)
Chronic non-tender swelling of the parotid and may be other salivary glands
Sarcoidosis
Severe dryness of mouth + mucositis + candidal infection
Post-irradiation
Mucoepidermoid carcinoma, adenoid cystic carcinoma, polymorphous low-grade adenocarcinoma, carcinoma ex pleomorphic adenoma all ex of
Malignant salivary gland tumors
Pleomorphic adenoma (Benign mixed tumor), Warthin’s tumor, monomorphic adenoma, Canalicular adenoma are ex of
Benign salivary gland tumors
Most (65%) of salivary gland tumors are found in the
Parotid gland
Accessory gland tumors are mostly found in the
palate
anatomic distribution of salivary gland tumors
1) Parotid (65%)
2) Accessory (25%)
3) Submandibular (10%)
4) Sublingual (<1%)
T or F: Salivary gland tumors are mostly Benign.
True (60%)
Most common salivary gland tumor is
Pleomorphic adenoma
Parotid gland is ____ benign
2/3
Submandibular is ____ benign
1/2
T or F: Sublingual gland tumors are mostly malignant.
T
Palate tumors are ____ benign
1/2
Upper lip tumors are mostly
benign
Lower lip tumors are mostly
malignant
Retromolar area tumors are mostly
malignant
Clinical cystic presentation could be
mucocele, ranula, cystic tumors
Ulcer clinical presentation could be
Necrotizing sialometaplasia, neoplasms
Mucoceles are mostly found on
the lower lip (80%)
Mucoceles are most common in what decades
1st-3rd
Mucoceles are caused by
trauma, laceration of salivary excretory salivary duct, mucin spillage into tissue.
Mucoceles exclusively affect ______ glands
minor
Clinical presentation of mucoceles
Dome-shaped, translucent/bluish nodule, fluctuant, often increasing and decreasing in size
Less common that conventional mucocele, appear as small blisters, often burst/heal and recur
superficial mucocele
Mucocele of ventral surface of tongue
Cyst of Blandin Nuhn
Mucocele tx
surgical excision of swelling and damaged salivary glands.
Location of mucous pooling in ranula is dicated by
mylohyoid clinical presentation
Ranula tx:
excision of mass and associated sublingual gland
Mucocele in FOM
Ranula
A true cyst of salivary duct origin
Salivary duct cyst (mucous cyst, mucous retention cyst)
Most common sites of Salivary duct cyst
Palate, FOM
Salivary duct cysts rarely can be _____ cyst in major glands. (polycystic disease of parotid gland)
congenital
Treatment of salivary duct cyst
simple excision
Salivary duct cyst pathology
Uni- or multilocular cyst with glandular epithelial lining
Mucous cysts are lined by
simple glandular epithelium
Histologically has epimyoepithelial islands and lymphatic destruction of acini
Sjogren’s
Increased RF, ANA, SS-A, and SS-B
Sjogren’s
Autoimmune disease characterized by autoantibodies against salivary ductal cells
Sjogren’s
Dry mouth and eyes with or w/o parotid tumor-like swellings
Primary Sjogren Syndrome (Sicca Syndrome)
Dry mouth, eyes, and any collagen-vascular disease (RA, Lupus)
Secondary Sjogren Syndrome
Sjogren’s patients have a 40 fold increased risk in developing
B cell non-hodgkin lymphoma
How to diagnose Sjogren’s
1) Blood work (ANA, SS-A, SS-B, RF)
2) Sialography (contrast medium)
3) Schrimer test (tears)
4) Salivary biopsy (lymphocitic infiltration of normal salivary glands)
Schrimer test should wet
<5 mm in 5 mins
Rose Bengal score ___ according to van Bijsterveld system
> 4mm
Salivary biopsy needs atleast ____ foci of periductal lymphocytes, ____ cells/4mm^2
2, 50
T or F: Salivary biopses are not consistently positive in pts with Sjogren syndrome. About 50% in labial salivary and 90% in parotid.
T
Lab findings RH
75
Lab findings ANA
90
Lab findings SS-A
80
Management of Sjogren Syndrome
Topical oral moisterizers, antifungal for candidiasis, restorative tx, immunosuppressive tx for associated autoimmune disorders, Periodic re-eval, FNA if needed to confirm or r/o lymphoma
The most common malignant salivary gland neoplasm
Mucoepidermoid carcinoma
Mucoepidermoid carcinoma in bone is called
Central mucoepidermoid carcinoma
Mucoepidermois tumors are composed of varying ratios of both
epidermoid and mucous cells
Ulcerated mass with blue compressible areas:
Mucoepidermoid carcinoma
Mucoepidermoid carcinoma is most common in
Parotid gland
T or F: Mucoepidermoid carcinoma can be asymptomatic or w/ pain, parasthesia
T
Mucoepidermoid carcinoma is the most common
Salivary, intraoral, pediatric, and intraosseous gland malignancy
T or F: Mucoepidermoid carcinoma is the 2nd most common salivary gland neoplasms
T
- 10-15% of all neoplasms
- 30% of all malignancies
Mucoepidermoid carcinoma is graded low, intermediate, high and depends on
1) Ratio of mucous cell vs epidermoid cells
2) Cystic vs solid
3) Degree of cytologic atypia
Lower grade mucoepidermoid carcinoma is identified by
more mucous cells and more cystic areas.
Mucoepidermoid carcinoma tx
depends on histologic grade, location, and clinical stage
Mucoepidermoid carcinoma can seemingly present as a
mucocele (especially in retromolar area)
An ulcerated mass that proliferates quickly
“Non-Hodgkin lymphoma”
3rd most common malignancy, low grade malignant salivary gland neoplasm
Polymorphous low-grade adenocarcinoma (PLGA)
PLGA is usually found in
minor salivary glands
PLGA is found more in
Females than males
Why is PLGA called polymorphous?
varied morphologic growth patterns microscopically
PLGA tx
complete excision
PLGA ____ metastasize
rarely (10%)
PLGA local recurrence rate
30%
Palatal mass with “orange peel” surface texture
PLGA
PLGA different histologic growth patterns
tubular, cribiform, solid, single cell files
Most common neoplasm of minor salivary glands
Pleomorphic adenoma (40%-most commonly on palate)
Pleomorphic adenoma (mixed tumor) characterized by
PLAG1 and HMGA2 rearrangements
Pleomorphic Adenoma is “pleomorphic” bc
- varied types of tissues noted (epithelial, cartilage, bone)
- Striking variability between tumors
Pleomorphic adenoma (mixed tumors are a mixture of
epithelial and mesenchymal elements (bone, cartilage, fat)
Malignant transformation of Pleomorphic adenoma occurs in ____ of pts
10%
Time period for malignant transformation is __
20 years
T or F: Pleomorphic adenoma malignant transformation rarely occurs in the oral cavity bc early clinical detection
T
Risk factors for malignant transformation of pleomorphic adenoma
-Longevity and recurrence, histological hyalinization, increased mitotic activity
Features that are NOT associated with malignant transformation of PA
capsular violation, increased cellularity, areas of necrosis
Invasive carcinoma ex-PA happens at
> 5mm
A benign salivary gland tumor w/ limited growth potential
Warthin’s Tumor
Tumor with strong association in adult men and smoking
Warthin’s tumor
Second most common tumor in parotid after PA
Warthin’s tumor
Warthin’s tumor is most likely to be found in which gland?
Parotid
T or F: Pathogenesis of Warthin’s tumor is unknown
T
-May be entrapped salivary gland w/in intraparotid lymph nodes
Frequently “multicentric” tumor within the same gland
Warthin’s tumor
Warthin’s tumor presents microscopically as
prominent cystic spaces w/ intraluminal papillary projections and lymphoid-rich stroma
Well-demarcated mass w/ papillary structures outline by rows or columnar cells, cystic spaces, and lymphoid stroma
Warthin’s tumor
High grade salivary gland cancer (regardless of histologic variant)
Adenoid cystic carcinoma
Tendency for neural invasion
Neurotripism
Slow-growing, but w/ symptoms of pain, numbness, nerve paralysis owing to tendency for local invasion and seeding outside primary mass
Adenoid cystic carcinoma
High rate of recurrence and late metastasis (after >10 yrs)
Adenoid cystic carcinoma
Firm mass of parotid, palate with pain/anesthesia due to neurotripism
Adenoid cystic carcinoma
Pathology variants of adenoid cystic carcinoma
Cribriform, tubular, solid, mixed patterns
Tx of Adenoid cystic carcinoma
wide sx excision, associated with overall poor prognosis
Adenoid cystic carcinoma most likely to be found in
parotid gland
Common “swiss cheese” pattern histologically
Adenoid cystic carcinoma
Sialolithiasis most commonly found in
submandibular gland
Calcification within the salivary gland/duct
Sialolithiasis
How does Sialolithiasis start?
Viscous mucus plug, bacteria, cellular debris-> mineralizes
T or F: Sialolithiasis is a localized process and has no relation to hypercalcemia (kidney/gall stones)
T
Risk factors for Sialolithiasis
hyposalivation/xerostomia
Major gland Sialolithiasis clinically presents as
tender swelling during meal times
Minor gland Sialolithiasis clinically presents as
Firm, often asymptomatic but may cause tenderness or swelling
____ films most helpful for Sialolithiasis
occlusal
-Not all stones sufficiently calcified to be visible
Cross section of Sialolithiasis reveals
concentric laminations
Ductal epithelium becomes ______ with Sialolithiasis
squamatized
Non invasive removal of sialiths
- gland massage, “milking” technique
- Sialagogues
- Infection and purulent discharge in long-standing cases: prescribe antibiotic
Surgical invasive removal of sialoliths
- Intraoral approach under local anesthesia
- Incision & removal of stone.