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349 Cards in this Set

  • Front
  • Back
Cyst Histology
(True Cyst)
A true cyst has an epithelial lining that surrounds a central cavity (simple stratified squamous)
Odontogenic Cysts
These cysts are derived from the tooth forming epithelium within the jaws
Radicular Cyst
-Aka Periapical cyst
-Inflammatory origin (inflammation, subsequent to the presence of bacteria in the periodontal ligament area, stimulates the epithelial rests of Malassez, which creates Hertwig's epithelial root sheath)


Can occur at the bottom or sides of the root
Stratified squamous epithelium

Bacteria may cause ulceration in the eipthelium & may allow cholesterol to accumulate
2 Most Common Cysts
1. Radicular cyst --> at the apex or side of the root
2. Follicular (Dentigerous) cyst --> not caused by inflammation or bacteria; most often seen around the crown of impacted teeth
Periradicular Cyst
Radiolucency at the apex of a non-vital tooth (this radiographic appearance can be many things)

Must remove all cyst material when extracting a tooth or a residual cyst will develop

Lined with epithelium, but most is connective tissue
4 Most Common Inflammatory Cells in a Periradicular Cyst
Neutrophils, Lymphocytes, Histiocytes, Plasma cells
Rests of Malassez
Oxygen diffuses through the rests
Dentigerous Cyst
-Forms around the crown of an impacted tooth (often attached to the CEJ upon extraction)
-Considered to be developmental in origin (error during development)
-Stratified squamous epithelium
Dentigerous Cyst
(Mechanisms of Development)
1) Degeneration of the stellate reticulum of the enamel organ
2) Accumulation of the fluid between the reduced enamel epithelium & the crown of the tooth
Concerns for leaving in third molars
-epithelium lining the cyst can turn into some other problem epithelium transforms into something bad (ameloblastoma, squamous cell carcinoma etc)
-if cyst size increases it can cause jaw fracture
Dentigerous Cysts
-rubbery in feeling
-may have pathologic fracture during removal
-during the teenage years there are hormones that will cause the cysts to grow very large
-cholesterol in cyst wall and giant cells
Eruption Cyst
-usually present in children
-most common around incisors or 1st mandibular molars
-presents clinically as a bump on the crest of the alveolar ridge where a tooth should be
-a radiograph will confirm the diagnosis
-on the crest of the ridge where the tooth should be
-tooth will erupt and the bump will go away, normal and will go away
Residual Cyst
-left over cyst from an extraction that doesn't get the remaining cyst tissue from a previous radicular or dentigerous cyst
Lateral Periodontal Cyst
-developmental cyst that arises from the rest of the dental lamina
-the intrabony counterpart of the gingival cyst of the adult
-most common in the mandibular premolar-canine-lateral incisor area
-thin epithelial lining with focal thickenings
Gingival Cyst of the Adult
-arises form remnants of the dental lamina (Rests of Serres)
-is primarily a soft tissue lesion
-it is a soft, freely movable, painless mass which sometimes has a bluish tinge
-it may erode cortical bone
Gingival Cyst of the Newborn
-white/pink papules on the alveolar mucosa of neonates
-histologically they display flattened epithelium with a parakeratotic surface.
-lumen contains keratinaceous debris
Cause of Gingival Cyst of Newborn
-alveolar mucosa has invaginations, keratin containing dead cells build up and they get stuck in the invaginations of the surface.
-they do go away with time when palpated they are some what firm
Palatal Cysts of the Newborn
-aka Epstein's pearls:white papules in the midline of the palate
-Bohn's nodules: white papules in multiple non-midline palatal locations
Odontogenic Keratocyst
-called OKC for short
-Recently renamed by the WHO to reflect its aggressive behavior compared to other odontogentic cysts
-NEW NAME: Keratocystic odonotgenic tumor (KCOT)
-considered to be primordial cysts
-develop where a tooth otherwise would
Histologic Criteria for KCOT
-corrugated layer of parakeratin lining the certain cavity
-6-8 cell thickness of the epithelial lining
-prominent palisading of basal cell nuclei
OKC treatment
-mandate more aggressive treatment and follow-up than other odontogenic cysts:
-peripheral ostectomy
-6 month radiographic follow-up
OKC associated with syndrome
-NEVOID BASAL CELL CARCINOMA SYNDROME (Gorlin syndrome)
-multiple OKC's
-multiple basal cell carcinomas
-epidermal cysts of the skin
-palmar/plantar pits
-rib anomalies
*can kill pt
Nevoid Basal cell carcinomas
-appearance like acne,can invade through the scalp and go through the bone and go into the brain and cause a hemorrhage, can invade into the eye and may have to remove the eye in order to remove these
Gorlin Cyst renamed
-renamed to calcifying cystic odontogenic tumor due to its more aggressive behavior
-bone looks moth eaten, normally can be removed with a peripheral ostectomy
Ghost Cells
-cant see nuclei where there should be nuclei
-more in the mandible than the maxilla
Nasopalatine Duct Cyst
-most common fissural cyst
-located in the midline of the anterior hard palate
-do vitality testing, molars take longer to respond
-can get a cyst in the soft tissue only
-stratified squamous epithelial lining with connective tissue wall
-collagen, numerous vascular channels
Nasopalatine Duct Cyst Appearance
-inverted pear shape
-take an x-ray to see what is happening in the bone
-sclerotic border (very white area around the cyst)
-teeths 8&9 should test vital
Lymphoepithelial Cyst
-most frequent locations- floor of mouth and posterior lateral tongue
-color- light yellow
-size: small, less than 6mm
-lymphoid tissue present
-caused by invagination of epithelium in which keratin is trapped (similar to epstein pearls)
-should remove to ensure it isnt malignant (epithelium lining this can transform into something malignant)
Mucocele
-pseudocyst created by trauma
-most common location - lower lip
-Clinical features-pale bluish translucent fluctuant lesion
-remove pool of mucin and gland associated with it.
-can have macrophages on periphery waiting to engulf mucin
Ranula
-essentially a mucocele in the floor of the mouth
-named after a frog's belly
Thyroglossal duct cyst
-located in neck
-caused from residual thyroglossal duct that failed to resorb
Dermoid cyst
-developmental true cyst, with keratin in the middle
Periapical granuloma
-sequela of dental caries
-identical etiology to the radicular cyst, but there is no epithelium bc the rest of Malassez have not proliferated
-resorption of bone, creating a radiolucent lesion, is caused by the inflammatory process
-teeth usually require extraction and site needs curetting
-sclerotic border
Median Palatal Cyst
-fissural cyst in the midline of the hard palate
-locatd posterior to palatine papilla
-lined by stratified squamous or respiratory epithelium
-not very common compared to nasopalatine cyst
-occurs because two halves of the palatal shelves are coming together and epithelium fails to breakdown and is caught between the two shelves, creating rest cells
-related to vital teeth
Globulomaxillary Cyst
-fissural cyst that does not exist
-inverted pear shaped radiolucency between maxillary lateral incisor and canine
-now believed to be : lateral periodontal cyst, lateral radicular cyst, or KCOT (keratocystic odontogenic tumor)
-conceptual error in embrologic development
Nasolabial Cyst
-may arise from remnants of the nasolacrimal duct or from fusion of the maxillary, median nasal and lateral nasal processes
-clinically presents as a swelling in the nasolabial fold area
-lined by respiratory epithelium
-present in younger individuals because it is a developmental cyst and grows slowly over time
-rubbery mass
-not very common
-doesn't transform into a malignancy
Midline Mandibular Cyst
-median mandibular cyst, or glandualr odontogenic cyst
-not associated with inflammation or dead teeth
-not developmental in origin
-considered rather aggressive, and can be considered a low grade mucoepidermoid carcinoma
-must be removed in block where a chunk of the mandible is removed so that it doesnt come back
Branchial Cleft cyst
-lesion of the lateral neck in young adults
-located in cervical lymph node chain area close to the anterior border of the SCM
-lined by stratified squamous epithelium or respiratory epithelium and surrounded by lymphoid tissue
-more common in males
-grows for years until large enough to be visible/palable
-can become secondarily infected via skin
Pseudocysts
-Aneurysmal bone cyst
-traumatic bone cyst
-stafne bone cyst
-mucocele (in soft tissue)
-ranula (in soft tissue)
*not lined by epithelium
Traumatic Bone cyst
-painless radiographic lesion: unicystic radiolucency scalloping around tooth roots
-teeth must be vital
-etiologic theory: trauma which does not cause fracture creates an intraosseous hematoma that liquefies and causes a defect
-histology: bone and CT fragments
-Tx: vigorous curettage to stimulate bleeding, radiographic follow-up
Aneurysmal Bone cyst
-radiolucency which may cause a blow out distention of the affected bone
-expansile and more common in the mandible
-Histology : cystic lakes of blood surrounded by fibrous CT with giant cells
-in young ppl (25 and younder)
-high recurrence rate
-looks like a lot of air in bone
Stafne Bone Cyst
-normal anatomy masquerading as a pathologic condition
-concavity of bone and not true space,
- due to submandibular gland pressing against adjacent bone
-not tx required
Classification Epithelial Odontogenic Tumors
-Ameloblastoma: benign
1. unicystic
2. traditional
-Amelobalstoma -Malignant
1. malignant ameloblastoma
2. ameloblastic carcinoma
-clear cell odontogenic carcinoma
-calcifying epithelial odontogenic tumor
-squamous odontogenic tumor
Histologic Criteria of Ameloblastoma
1. Stellate Reticulum
2. columnar ameloblasts with nuclei polarized toward the stellate reticulum
3. apical clearing of the cytoplasm of the columnar ameloblasts
Unicystic Ameloblastoma
-arises within the epithelium of a dentigerous cyst
-can be treated more conservatively than conventional ameloblastoma
-should not be treated conservatively if there is a mural component
calcifying epithelial odontogenic tumor
radiographic features
-also called pindborg tumor
-considerable variation
-uniocular or multilocular
-flecks of calcium ("dirven snow")
-can be radiolucent
-50% associated with unerupted tooth
-root resorption common
Calcifying epithelial odontogenic tumor (pindborg)
microscopic features
-considerable variation
-polyhedral epithelial cells
-intercellular bridges often prominent
-cementum-like lamellar calcifications
-homogeneous eosinophilic substance
Calcifying Epithelial Odontogenic Tumor (pindborg)
Treatment and Prognosis
-slow growth, locally invasive
-no metastic potential
-few cases w/long term follow up
-recurrence rate 14%
-complete, conservative removal
Mixed Odontogenic Tumors
1. Adenomatoid odontogenic tumor
2. ameloblastic fibroma
3. ameloblastic fibro-odontoma
4. ameloblastic fibrosarcoma
5. odontoameloblastoma (ameloblastic odontoma)
6. compound odontoma
7. complex odontoma
Adenomatoid Odontogenic Tumor (AOT)
-location in anterior maxilla
-asymptomatic radiolucency with Radioopaque flecks
-around the crown of impacted canines
-Histo: whorled masses of ondontogenic epithelium which form duct-like structures
-foci of calcification
-nuclei of the cuboidal or columnar cells are polarized away from the duct-like central areas
Adenomatoid Odontogenic Tumor facts (AOT)
-affects younger patients: two thirds are 10-19
-anterior jaws-usually maxilla
-in 75% of cases, the tumor presents as a circumscribed RL, usually around the crown of an impacted tooth, most often a canine
AOT additional Histo
-amorphous eosinophilic material may represent amyloid
-central area of cavitation where tooth crown was located
Compound Odontoma
-Age: 10-20 years
-Location: anterior maxilla
-Clinical: Asymmetrical eruption pattern
-Radiograph: <1 cm radiopacity in tooth-bearing area
-Gross appearance: Multiple "toothlets"
-Histo: Regular enamel, dentin an dpulp
-Tx: conservative removal
Complex Odontoma
-Age: 10-20 years
-Location: posterior mandible
-Clinical: eruption asymmetry
-Radiograph: Irregular radiopacity
-Haphazard deposition of enamel, dentin, pulp-like tissue, often surrounded by odontogenic epithelium
-Tx: conservative removal
Ameloblastic fibroma
-Age <20 years
-Location: Mandible (molar/premolar area)
-clinical: painless swelling
-Radiographic: circumscribed radiolucency
-Histology: Pulp-like immature stroma with islands of ameloblastic epithelium
-Tx: through conservative surgical removal
Ameloblastic fibro-odontoma
-age <20 years
-locations: posterior jaws, more frequently the mandible
-Clinical: painless swelling
-Radiographic: Circumscribed RL containing "spiky" radiopacities associated with the crown of an impacted tooth
-Histo: that of ameloblastic fibroma plus odontoma
-Tx: thorough conservative surgical removal
Two exceptions to posterior mandible rule
-AOT and Compound Odontoma- these are both usually found in the anterior maxilla as oppposed to the posterior mandible
Odontogenic Tumors of ectomesenchyme
-Odontogenic Fibroma
1. simple
2. WHO type
-Granular cell odontogenic tumor
-odontogenic myxoma
-cementoblastom
odontogenic fibroma WHO type
-45% of lesions in maxilla (in maxilla, the tumors are located more anteriorly)
-mandibular tumors are usually posterior to the first molar
-Radiolucent lesions
-Histo: dense collagen with interspersed odontogenic epithelial rests and small cementum-like calcifications or dentinoid
HPVs
-double stranded DNA viruses of the papovavirus subgroup A
-they are capable of integrating with the host cell DNA or may exist episomally within the affected cell
-over 100 known HPV subtypes
Benign Oral Epithelial Lesions related to HPV infection
-squamous papilloma
-condyloma acuminatum
-verruca vulgaris
-focal epithelial hyperplasia
Relationship of Specific Viral Subtypes to Specific Lesions
-squamous papilloma 6,11
-condyloma acuminatum 6,11, 16,18
-verruca vulgaris 2,4,40
-focal epithelial hyperplasia 13, 32
Squamous Papilloma
-papillary projections of any shape
-hyperparakeratosis
-acanthosis
-mild basilar hyperplasia and scattered mitotic figures
-mild chronic inflammatory cell infiltrate in connective tissue
Verruca vulagris
-autoinnoculation is a common type of spread
-usually in children
-spreads most commonly to oral mucossa from hands
Verruca vulgaris
-autoinnoculation is a common type of spread (people try to smash it)
-usually in children
-spreads most commonly to oral mucosa from hands
Verruca vulgaris histology
-hyperorthokeratosis
-hypergnaulosis
-koilocytes in superficial spinous layer
-convergence of rete ridges toward center
verruca vulgaris treatment
-conservative excision
-cryotherapy
-keratinolytic agents
-two thirds spontaneously disappear within two years
Condyloma acuminatum
-20% of STD's
-genital, perianal, laryngeal, oral
-sessile, pink, short, blunt, papillary projections
-labial mucosa, soft palate, lingual frenum and uvula are common locations
Focal Epithelial Hyperplasia (heck's disease) Histology
-slight papillary appearance
-marked acanthosis
-broad rete ridges
-mitosoid or mitotic cells in spinous layer
Focal epithelial hyperplaisa (heck's disease) treatment
-conservative excisions
-spontaneous regression has been reported
Verruciform xanthoma
-a hyperplastic condition of the epithelium with a characteristic accumulation of lipid laden histiocytes with the connective tissue
-etiology unknown, although NOT associated with HPV
-may be due to localized epithelium trauma
Verruciform xanthoma facts
-age: 40-70 years
-Sex: female predilection 2:1
-sites: gingiva and alveolar mucosa are most common
-Clinical features: Painless, sessile, well-demarcated mass with a roughened surface. Color may vary from white to yellowish to red.
Verruciform xanthoma treatment
-simple excision
-prognosis: excellent
-caveat: two cases have been reported where a VX was associated with a squamous cell carcinoma or carcinoma in situ
Keratoacanthoma ("self-healing carcinoma")
-Etiology: Sun damage and HPV (36,37)
-Clinical: On sun-exposed skin in patients over 45 years of age
-Firm, non-tender, well-demarcated nodule with a central keratin plug that is yellowish, brown or black with a verruciform surface
Keratoacanthoma
-will regress spontaneously with scarring
-since it looks like cancer should one wait to see whether it regresses? NO
- most frequently located on the vermillion border at junction of vermilion and the skin
-rapid enlargement occurs to 1-2 cm within 6 weeks
-lesions regress 6-12 months from onset
Keratoacanthoma Histiology
-surface epithelium at lateral edge is normal
-hyperparakeratotic verruciform stratified squamous epithelium centrally with broad bands of epithelium growing downward.
-margins are constricted at the surface to give an "ice-tong" effect.
-pronounced chronic inflammatory response which demarcates the lesion
-lesion is said to be "crater-like"
HPV detection
-immunohistochemistry
-in situ hybridization
-polymerase chain reaction
High risk HPV's
-16 and 18
-have been associated with uterine cervical, anogenital and oropharyngeal cancers
-GARDASIL vaccine is now available in the US for HPV 6,11, 16 and 18 targets very young women
Premalignant and malignant lesions related to infection with HPV
-koilocytic dysplasia
-verrucous carcinoma
-squamous carcinoma
Squamous cell carcinoma of the anterior 2/3s of the oral cavity =
much less likely to be due to HPV
Verrucous carcinoma
-long been related to smokeless tobacco, but can also harbor HPV
-presense of verrucous carcinoma in genital regions suggests an etiologic role for HPV
Proliferative Verrucous Leukoplakia (PVL)
1. assoicated with HPV
2. predominant in females
3. progresses to SCC
Oral Melanotic Macule
Etiology: Possibly trauma
Age: avg is 43
sex: femal predilection 2:1
site: vermilion border, buccal mucosa, gingiva and palate
Oral melanotic Macule Histiology
-Increased melanin in the basal layer
-melanophages in the connective tissue
-epithelium is normal
Oral melanotic Macule treatmetn
-should excise in order to rule out melanoma.cannot tell the difference on clinical appearance alone with early lesion
Melanotic Nevus
-begins to develop in childhood and most are present by age 35
-clinical appearance: localized brown to blue to black flat or raised non-enlarging lesions, most frequent on palate or maxillary gingiva
-not common intraorally, compared to the skin
Melanotic Nevus types:
Intramucosal
compound
junctional
blue
Melanotic Nevus Histo
-small rounded cells with benign nuclei and varying amounts of melanin in the cytoplasm lying singly, either at the junction between the epithelium and th connective tissue or entirely within the connective tissue
-blue nevi have spindle shaped nuvus cells
-nevus cells arise from the neural crest during development
Carcinoma in Situ
-top to bottom cellular abnormality
-most common as erythroplakia, clinically
-CIS in the oral cavity and pharynx will appear primariliy on non-keratinizing stratified squamous epithelium
-very curable because invasion has not occurred
oral cancer facts
-1 person dies every hour from oral cancer
-4 people per hour are diagnosed with head and neck cancer
Verrucous carcinoma
-associated with topical tobacco use (snuff dippers cancer)
-considered a low grade variant of SCC
-slow growing
-invades as a moving front
-associated with HPV 16,18,2,32
- up to 20% have been assoicated with conventional squamous cell carcinoma
Dysplastic nevus
-one considered to be premalignant
leukoplakia
-a white patch that cannot rub off and that cannot be identified as any other lesion
-this is clinical description only is NOT A diagnosis
Types of Odontogenic Cysts
-Radicular Cyst (periapical cyst, apical periodontal cyst)
-Dentigerous cyst (follicular cyst)
-Eruption Cyst (eruption hematoma
-lateral periodontal cyst
-gingival cyst of the adult
-ginigival cysts of the newborn (Epstein pearls, Bohn's nodules_
-Primordial cyst
-Odontogenic keratocyst
-Calcifying odontogenic cyst (Gorlin cyst & keratinizing and calcifying odontogenic cyst)
Types of Fissural Cysts
-nasopalatine duct cyst (incisive canal cyst)
-median palatal cyst (median palatine cyst)
-globulomaxillary cyst ( Avoid use of this term, no longer considered a TRUE fissural cyst)
Types of Soft Tissue Developmental Cysts
-Oral/lymphoepthelial cyst
-Branchial cleft cyst (lymphoepithelial cyst)
-Thyroglossal duct cyst
Types of Pseudocysts
-Aneurysmal bone cyst
-Traumatic bone cyst (unicameral bone cyst, solitary bone cyst, simple bone cyst, hemorrhagic bone cyst)
-Stafne bone defect (static bone cyst, lingual mandibular salivary gland depression)
-Mucocele (mucous extravasation or retention phenomenon)
-Ranula (retention cyst)
Periapical lesions that appear radiographically as cysts
-Dental granuloma (periapical granuloma)
-apical scar
Radicular Cyst: Age/Sex prevalence, clinical features,
-odontogenic
-aka periapical cyst or apical periodontal cyst
-Age/Sex: any age, M=F
-Clinical: either jaw, esp. in anterior maxilla at apex of non-vital teeth, may be painful esp. to percussion. May expand bone or erode cortex.
-Radiograph: Radiolucent compromising lamina dura and periodontal space.
-Cannot distinguish radiographically from dental granuloma
Radicular Cyst: Histology, treatment, prognosis
-Histology: cyst lined by stratified squamous epithelium, surrounded by chronic inflammation
-Treatment: endodontic therapy and apical surgery or extraction and apical curettage
-Prognosis: Good
Dentigerous Cyst: Age/Sex, Clinical
- aka follicular cyst
-Age/Sex: usually young adults <15yrs, M=F
-Clinical: impacted mandibular 3rd molars most often, followed by maxillary 3rd molars, then maxillary cuspids. Circumscribed radiolucency around crown of unerupted tooth. May result in jaw expansion.
Dentigerous Cyst: Histology, Treatment, prognosis
-Histology: cyst lining of squamous epithelium may be hyperplastic. Surrounding fibrous connective tissue contains islands of odontogenic epithelium.
-Treatment: complete removal
-Prognosis: good but follow patient, cyst may be source of odontogenic tumor or pathologic fracture.
Eruption Cyst: Age/Sex, Clinical
-aka eruption hematoma
-Age/Sex: mainly in children, M=F
-Clinical: over erupting teeth, soft, dome-like often red lesion; radiograph shows normal erupting tooth.
Eruption Cyst: Histology, Treatment, Prognosis
-Histology: Cyst-like lesion filled with sero-sanginous fluid rimmed by epithelium
-Treatment: no treatment, or conservatively remove overlying tissue
-Prognosis: Excellent
Lateral Periodontal Cyst: Age/Sex, Clinical
-may arise from rest of the dental lamina
-Age/Sex: any age, M=F
-Clinical: Mandible>maxilla, mandibular and maxillary premolar and cuspid areas; teeth vital. Usually, asymptomatic; occasionally painless swelling; radiographically a well circumscribed radiolucency on lateral surface of a tooth; may be multiloculated (botryoid odontogenic cyst)
Lateral periodontal Cyst: Histology, Treatment, Prognosis
-Histology: Cyst lined by thin epithelium with occasional focal thickenings with clear cells. There is no inflammation in the cyst wall
-Treatment: Complete removal
-Prognosis: Excellent, recurrence unlikely
Gingival Cyst of Adult: Age/sex, Clinical
-arises from rests of the dental lamina
-Age/Sex: adults, M=F
-Clinical: mandibular premolar region in soft tissue. Soft freely movable, painless mass. May erode cortical bone and show shadow on radiograph.
Gingival Cyst of Adult: Histology,Treatment, Prognosis
-Histology: Same a lateral periodontal, but located beneath the mucosal epithelium within the soft tissue
-Treatment: complete removal
-Prognosis: excellent recurrence unlikely
Gingival Cysts of the Newborn: Age/Sex, Clinical
-includes epstein's pearls, Bohns nodules
-Age/Sex: newborn, M=F
-Clinical: Superficial white papules on the alveolar mucosa of infants (GCN) the midline of the palate (EP) or the lateral hard and soft palate (BN)
Gingival cysts of Newborn: Histology, Treatment, prognosis
-Histology: cyst lined by parakeratotic epithelium with central keratinaceous debris
-Treatment: no tx, cysts involute as infant grows
-Prognosis: Excellent
Primordial Cyst: Age/Sex, Clinical
-a cyst which develops where a tooth would have formed
-Age/Sex: any age, but usually adults. M=F
-Clinical: Mandible>maxilla, third molar region most often
Primordial Cyst: Histology, Treatment, prognosis
-Histology: cyst lining of stratified squamous epithelium that is often keratinized. Fibrous connective tissue usually not inflamed. Does not have basal layer palisading.
-Treatment: complete removal
-Prognosis: Good but follow patients
Odontogenic Keratocyst: Age/Sex, Clinical
-Age/Sex: Majority between 10 and 40 years of age, but can occur at any age, M>F
-Clinical: 60%-80% in mandible usually posterior and ascending ramus, sharply circumscibed radiolucency, either unilocular or multilocular
Odontogenic Keratocyst: Histology, Treatment, Prognosis
-Histology: corrugated parakeratinized stratified squamous epithelial lining of 6-8 cells in thickness. Prominent hyperchromatism and palisading of the basal layer.
-Treatment: Complete removal
-Prognosis: Moderate to good, Carefully follow, recurrence rate high (33-50%) Rule out nevoid basal cell carcinoma syndrome.
Carcinoma in situ
-top to bottom cellular abnormality
-most common as an erythroplakia clinically (sublingual caruncles)
-CIS in the oral cavity and pharynx will appear primarily on non-keratinizing stratified squamous epithelium
-very curable because invasion has not occured
Smokeless tobacco facts
-1 person dies every hour from oral cancer
-4 people per hour are diagnosed with head and neck cancer
Verrucous carcinoma
-associated with topical tobacco use
-nicknamed "snuff dippers cancer"
-low grade variant of SCC
-slow-growing
-invades as a "moving front"
-associated with HPV 16,18,2,32
-up to 20% have been assoicated iwth conventional squamous cell carcinomas
Nuvus
-intradermal (intramucosal)
-compound
-unctional
-dysplastic nevus: one considered to be premalignant
Melanoma
-use ABCD crteria to determine need for biopsy
Verruciform xanthoma
-hyperplastic condition of epithelium with a characteristic accumulation of lipid-laden histiocytes within the connective tissue
-etiology unknown, although not associated with HPV
-may be due to localized epithelial trauma
-benign epithelial neoplasm
-40-70 years
-females 2:1
-gingiva and alveolar mucosa most commonly
-painless, sessile, well-demarcated mass with a roughened surface. color may vary from white to yellowish to red
-simple excision w/excellent prognosis
-2 cases reported wher a VX was associated with SCC or CIS
keratoacanthoma ("self-healing carcinoma")
-benign epithelial neoplasm
-sun damage and HPV (26,37)
-on sun-exposed skin in patients over 45 yrs
-firm, non-tender, well-demarcated nodule with a central keratin plug that is yellowish, brown or black with a verruciform surface
-regress spontaneously with scarring
- should biopsy because looks like cancer
-frequently located on vermilion border at the junction of the vermilion and the skin
-rapid enlargement occurs to 1-2 cm within 6 weeks
-lesions regress 6-12 months from onset
keratoacanthoma Histology
-surface epithelium at lateral edge appears normal.
-Hyperkeratotic verruciform stratified squamoust epithelium centrally with broad bands of epithelium growing downwards. Margins are constricted at the surface to give an "ice-ton" effect. Pronounced chronic inflamatory response which demarcates the lesion. Lesion is said to be "crater-like"
Oral Melanotic Macule (focal melanosis)
-possibley from traume
-avg age is 43
-female 2:1
-should excise in order to rule melanoma. cannot tell difference on clinical appearance alone
Oral Melanotic Macule Histology
-increased melanin in the basal layer. Melanophages in the connective tissue. Epithelium is normal.
Melanocytic nevus
-begins to develop in chilhood nd most present by age 35
-localized brown to blue to black flat or raised non-enlargin lesions, most frequent on plalate or maxilary gingiva
-not common intraorally, compared to the skin
types: intramucosal, compound, junctional, blue
Melanocytic Nevus histology
-small rounded cells with benign nuclei and varying amounts of melanin in the cytoplasm lying singly or in theques, either at junction between the epithelium and the connective tissue or entirely within the connective tissue
-blue nevi have spindle shaped nevus cells
-nevus cells arise from the neural crest during development
-intramucosal nevus has no junctional activity
Leukoplakia
-a white patch that cannot rub off and that cannot be identified as any other lesion
-clinical description only Is NOT A DIAGNOSIS
Oral and Pharyngeal Cancer
-6th leading sie globally
-2nd leading site in men in southeast Asia
-31,000 new cases each year in USA
-4th leading cancer in black men
-7th leading cancer in white men
-9,000 deaths each year
-90% SCC
-90% over 45 years of age
Oral cancers can resemble benign lesions
-malignancies initially presumed to be benign lesions can cause delays in diagnosis
Advanced Cancers: tongue and mouth floor
-patients used tobacco and drank alcohol
-diagnosis delayed more than five months
-agressive treatment: surgery & radiation
-patients survived less than six months
Diagnosis
-incisional biopsy (deifnitive diagnosis)
-adjunctive techniques
-toluidine blue (vital stain)
-chemiluminescence (vizlite)
-brush biopsy
Toluidine Blue Mechanisms
-binds to DNA and sulfated mucopolysachharides
-both high in malignant and dysplastic cells
-electrical potential of mitochondrial membranes
-negative charged membranes atract dye and are high in malignant and dysplastic cells
-technique: rinse, apply 1% toluidine blue, rinse, apply 1% acetic acid, rinse
Chemiluminescnece (ViziLite)
-low energy, low wave length light (430-580 nm)
-pretreat epithelium with 1% acetic acid
-dehydrates cytoplasm; cells more dense
-dysplastic and malignant cells of squamous epithelium of the cervix appear as "acetowhite"
Brush Biopsy Technique
-description analysis of cells representing full thickness of stratified squamous epithelium
-topical or local anesthesia is not required- minimal or no pain
-slightly moisten the biopsy brush with water or the patient's saliva if the lesion is dry
-the flat surface or cylindrical edge of the biopsy brush is placed against the surface of the lesion
-apply firm pressure against the surface of the lesion while rotating 5-10 times
-pink tissue or micro-bleeding indicates that the brush has penetrated to the desired depth, the basement membrane
Brush biopsy report
-negative: no cellular abnormalities
-positive: definitive cellular evidence or epithelial dysplasia or carcinoma
-atypical: abnormal epithelial changes warranting further investigation
Early detection of oral cancer
-clinical features: ulcer, lump, white and/or red changes
-may be with or without symptoms
-diagnosis: incisional biopsy adjunctive techniques
oral Squamous carcinomas: problems in early detection
-squamous cell carcinomas account for more than 90% of oral cancers
-these carcinomas can resemble numerous benign lesions
Histopathology
-more than 90% of oral cancers are SCC
-normal histology reflects regulated maturation of epithelial cells
-dysplasia reflects discrepancy in maturation
-SCC reflects invasion of connective tissue
Precancerous Lesions
-leukoplakia, erythroplakia, erythroplakia
-recognizing and treating these lesions with a risk for malignant transformation may prevent some oral cancers from occuring
-risks of different clinical forms
-Histopathology: hyperkeratosis, dysplasia
-management: surgical
leukoplakia forms
-homogeneous
-erythroleukoplaki
-dysplasia
-frictional
-candidal (cancer risk?)
-proliferative verrucous
Proliferative Verrucous leukoplakia
-diagnosis: clinical-microscopic
-women non smoking, elderly
-HPV 16
-malignant transformation >50%
-management: surgical, chemoprevention ineffective
Importance of Follow up
-all leukoplakias should be followed since even seemingly innocuous appearing lesions (asymptomatic hyperkeratosis) may transform to carcinoma with time
Leukoplakia Control
-remove irritant
-definitive diagnosis
-adjunctive techniques
-treatment, surgical, chemoprevention, follow-up
-re-biopsy if change in signs and/or symptoms
Screening
The application of a test or tests to people who are apparently free from the disease in question in order to sort out those who probably have the disease from those who probably do not
Case-finding
A diagnostic test or method that is applied to a patient who has abnormal signs and symptoms in order to establish a diagnosis and bring the patient to treatment
Velscope
hand held device that is based on the direct visualization of tissue fluorescence and the changes in fluorescence that result when abnormal tissue is present. Healthy tissue appears bright green and abnormal tissue will appear dark
Trimera visual detection
-Brilliant white- to detect lesion
-violet-normal blue, abnormal tissue dark
-amber/green- to show vascular pattern
Problems with visual detection
-velscope or vizilite or trimera
-brush biopsy
possible addition of up to $300 and 3 appointments vs 1 to final dx.
Effects of involuntary smoking
-25% greater than expected for women co-habitants
-35% greater than expected for men co-habitants
-20% greater than expected for non-smoking women exposed to smoking in the workplace
Smoking during pregnancy
increased incidence of:
-fetal death and stillbirth
-SIDS
-reduced fertility
-low birth weight
-placenta previa
-placenta abruption
-pre-term delivery
Bidis
-small brown cigarettes of tobacco hand-rolled in tendu leaf
-imported from india and southeast asia
-available in a variety of flavors
-produce higher tar and carbon monoxide levels
-nicotine concentration (21.2mg/g) significantly greater than traditional filtered cigarettes
-meta-analysis demonstrated increased risk for oral cancer for bidi smokers compared to non-smokers
Clove cigarettes-Kretek
-delivers significant quantities of nicotine and carbon monoxide
-taste, aromatic odor, and novelty contribute to appeal
-hemorrhagic pulmonary edema and aspiration pneumonia have been reported as a consequence of laryngeal anesthesia from eugenol
Hookah Bars
-increasingly popular social venue
-water cools the smoke and filters some of particulate matter
-nicotine levels rose from 1.11ng/ml at baseline to a mx of 60.31ng/ml 45 minutes
Spit tobacco
significant health risks
-numerous carcinogens
-nicotine addiction
-physical dependence
-withdrawal symptoms after abstinence
Nitrosamines in Spit Tobacco
Nitrosamines levels in spit tobacco are 10-100 times higher than the levels in the inhaled smoke from one cigarette and 20,000 times higher than the level allowed in food by the FDA and the department of Agriculture
non-oral cancers associated with spit tobacco use
-laryngeal cancer
-esophageal cancer
-colorectal cancer
-bladder cancer
Health risks assoicated with cigar smoking
-a cigar smoker's intake of nicotine and other toxins may exceed that of a typical cigarette smoker's
-cigar smoking is associated with increased risk of early death from coronary heart disease
-increased risk of lung cancer, oral cavity/pharyngeal cancer, laryngeal cancer, esophageal cancer
Smoking and Periodontal disease
-evidence suggests an immune mechanism exists whereby the effects of smoking on local and systemic immune factors may make the smoker more susceptible to bacterial infection
-substantial evidence also indicates that smoking impairs he regeneration and repair of periodontal tissues
-evidence is sufficient to infer a causal relationship between smoking and periodontitis
Nicotine effects
-increase in heart rate/blood pressure
-enhances information processing
-reduce fatigue
-sedative action
-reduces anxiety
-induces euphoria
Criteria for substance dependence dx
-development of tolerance
-withdrawal syndrome
-used in larger amounts or over a longer period than intended
-social, occupational, recreational activities reduced or given up
-use continues despite knowledge of problem
The dental team a perfect match for tobacco cessation
-22-40 yr old population more likely to have regular dental visits than physician visits and can benefit substantially from dental practice cessation efforts
-appeal of esthetics in conjunction with the practice of cosmetic dentistry is appealing
-recurrent follow-up visits provide opportunity
-#D1320- tobacco counseling for the control and prevention of oral disease
-tobacco prevention and cessation improves oral health
clincal practice
-identify, document and treat every tobacco user
-three types of behavioral conseling are effective: practial couseling, intra-tx, extra tx
-one or more pharmacoptherapies should be offered to all pts attempting to quit
The 5A's
-ask
-advise
-assess
-assist
-arrange (follow up)
behavior change
-individuals resist change
-faced with change, most people are not ready to act
-change is not a single step, but a process
-change may involve cyclic repetition
-intervention will be more effective if it is appropriate to he patient's readiness to change
The 5Rs to enhance motivation for patients not ready to quit
-Relevance
-Risks
-Rewards
-Roadblocks
-Repetition
Is Weight gain a roadblock
-fear of weight gain is cited as the reason for returning to smoking by 1/5 of male and 1/3 female smokers
-the average patient will gain 4-10lbs
-appropriate pharmacotherapy can help delay or decrease weight gain
-the average weight gain at 2 year tobacco-free anniversary is about 5lbs
Assiting the Patient
TRIPS
-Tirggers and challenges
-Reasons for wanting to quit
-Importance/confidence in ability to quit
-Pharmacotherapy and a quit date
-Social and emotional support
1st line pharmacotherapies
-safe and effective for tobacco dependence treatment, approved for use by US FDA
-NRT: gum, lozenge, patch, inahler, nasal spray
-buproprion SR
factors to consider when Rx Pharmacotherapy
-contraindications for individual patients
-patient preference
-patients previous experience with meds
-patient characteristics
co-morbidities (alcohol and drug use)
history of depression
concern about weight gain
NRT
-not recommended for use in adolescents or women who are pregnant or breastfeeding
-no evidence of increased CV risk with NRT except with acute disease
Major medical contraindications
-immediate myocardial infarction (<2 weeks)
-serious arrhythmia
-serious or worsening angina pectoris
-accelerated hypertension
Nicotine Gum
contraindicated in patients with TMJ disorders
-cause mouth soreness, hiccups, stomach upset, jaw aches
Nicotine Lozenge
-approved for OTC use in 2002
-delivers 25% more nicotine than equivalent gum dose
-nausea, headache, cough, heartburn, flatulence, hiccups
-have to be dissoved in mouth- 20-30 minutes
Nicotine Transdermal Patch
-lowest addiction potential of all NRTs
-delivers steady dose of nicotine
-available OTC and Rx
- headache, local skin reactions, vivid dreams
Nicotine Oral Inhaler
-Rx
-nicotine inhalation system
-replacs hand to mouth habit
Precautions
-asthma or chronic pulmonary disease
-recent MI, angina pectoris, serious arrhythmia or vasopastic disease
-severe renal impairment
-peptic ulcer disease
-hyperthyroidism, pheochromocytoma or insulin-dependent diabetes
most comon side effects
-mild and improve with time
-local irritation throat/mouth (40%)
-coughing (32%)
-rhinitis (23%)
Nicotine Nasal Spray
-Rx
-Highest addiction potential of all NRTs
Precautions
-reactive airway disease (asthma, bronchitis)
-chronic nasal disorders
-patients with a history of MI and/or angina pectoris, serious cardiac arrhthmias, or vasospastic disease
-hepatic or renal insufficiency due to reduced drug clearance
-use with caution in patients with endocrine disease as nicotine causes release of catecholamines by the adrenal medulla
-active peptic ulcer disease due to impaired healing
-accelerated hypertension
Side effects
-moderate to severe nasal irritation
-nasal congestion
transient change in sense of smell/taste
Buproprion SR
-marketed as Zyban for smoking cesation or Wellbutrin SR for depression
-doubles abstines rates vs. pacebo
-only non-nicotine medication approved by FDA for smoking cessation treatment
-mechanism: presumably blocks neural reuptake of dopamine and/or NE
Zyban contraindications
-seizure disorder or previous seizure
-current or prior diagnosis of anorexia or bullimia
-using an MAO inhibitor in previous 14 days
-using other medication containing buproprion
-patients undergoing abrupt discontinuation of alcohol or sedative (including benzodiazepines)
-other meds that lower the seizure threshold
side effects: insomnia and dry mouth
Epulis Fissuratum
-denture inury tumor
-official path dx: infammatory epithelial and fibrous hyperplasia (exophytic reactive lesions)
Exophytic reactive lesions
-epulis fissuratum
-inflammatory papillary hyperplasia
-pyogenic granuloma
-peripheral ossifying fibroma
-peripheral giant cell granuloma
-traumatic neuroma
-torus
Traumatic Fibroma
-focal fibrous hyperplasia
-buccal mucosa
-also on the tongue, but can be on any site exposed to trauma
-pink,firm,painless. has a smooth surface
-covering a stratified squamous epithelium
-connective tissue is composed of a nodule of excessive collagen
-little inflammation
-small vascular channels
Giant cell fibroma
-smooth surfaced pink papule
-gingiva, palate, lip, tongue
-characterized by unusual fibroblasts that are stellate with multiple nuclei. Collagen is often whorling or hyalinized
-treatment is excision. does not recur
Retrocuspid Papillae
-microscopically looks like giant cell fibroma
-normal anatomic variants
lipoma
-rare in the oral cavity
-non-ulcerated, painless
-surface is delicate and smooth and may exhibit small vessels
-soft and light yellow and most common on buccal mucosa
Granular cell tumor
-raised, non-ulcerated firm yellowish nodule
-most common on the tongue
-painless
-female predilection
-granular cells are positive for S-100 protein indicating tumor origin from the neural crest
-most distinctive microscopic feature is the psedoepitheliomatous hyperplasia (PEH), which can be mistaken for SCCA
-excisional biopsy can be transected at the deep margin and still not recur
congenital epulis of the newborn
-female predilection
-more common on maxillary gingiva
-soft, round exophytic mass attached to alveolar mucosa
-no pseudoepitheliomatous hyperplasia
-does not contain S-100 protein
-simple surgical removal
neurofibroma
-benign tumor of schwann cells
-painless, non-ulcerated
-intraoral lesions most commonly on tongue or palate
-smooth-surfaced, non-ulcerated
-look for signs of von Recklinghausen's disease
-usually a solitary tumor in adults
-patients with neurofibromatosis may die of sarcomas
Neurilemmoma
-circumscribed, smooth surfaced nodule
-pink
-location: tongue and palate are most comon
-encapsulated
-painless
-verocay body (histology)
Multiple endocrine Neoplasia Syndrome III
(Multiple Mucosl neuroma syndrome) (MEN III)
-multiple mucosal neuromas
-pheochromocytoma
-medullary carcinoma of the thyroid
-dentist can detect and save persons life
Mesenchymal tumors
-traumatic fibroma
-giant cell fibroma
-retrocusid papillae
-lipoma
-granular cell tumor
-congenital epulis of the newborn
-neurofibroma
-neurilemmoma
-multiple endocrine neoplasia syndrome III
-hemangioma
-lymphangioma
-cystic hygroma
-peripheral giant cell granuloma
-peripheral ossifying fibroma
Calcifying odontogenic cyst Age/Sex, Clinical
-aka Gorlin Cyst; keratinizing and calcifying odontogenic cyst
-Age/Sex: any age, second decade most often, either sex
-Clinical: May be cystic (86%) or solid (14%) intraosseous 87%, extraosseous 13% mandible>maxilla, may be associated with other odontogenic lesions and tumors; radiographically intraosseous COC's are seen as localized radiolucencies with varying amounts of radiodensities; extraoseous COC's are tender swellings
Calcifying odontogenic cyst Histology, Treatment and Prognosis
-Histology: Odontogenic epithelium; ghost cells adn dystrophic calcification. other odontogenic tissue/tumors may be found in association
-Treatment : complete conservative surgical removal
-Prognosis: Good. Recurrences are rare
Nasopalatine duct cyst Age/Sex, Clinical
- aka incisive canal cyst or if located in incisive papilla, cyst of palatine papilla
-most common non odontogenic cyst of the oral cavity
-Age/Sex: Adults, M=F
-Clinical: Mid-line of anterior maxilla; behind maxillary incisors, may be asymptomatic or may present as swelling with pt complaining of drainage. radiograph is heart shaped circumscribed radiolucency
Nasopalatine Histology, Treatment, Prognosis
-Histology: Cyst lined by repiratory and stratified squamous epithelium, surround connective tissues contains nerves mucous glands, thick walled vessels and perhaps cartilage
-Treatment: remove if symptomatic or >1.0cm in diameter radiographically
-Prognosis: good
Median palatal cyst Age/Sex, Clinical
-Age/Sex: Adults, M=F
-Clinical: midline of hard palate posterior to incisive canal. Firm or fluctuant swelling of midline of hard palate posterior to palatine papilla
Medial palatal cyst Histology, Treatment, Prognosis
-Histology: cystic space lined by squamous epithelium or respiratory epithelium surrounding connective tissue may contain chronic inflammatory cells
-Treatment: complete removal
-Prognosis : good
Globulomaxillary Cyst Age/Sex, Clinical
- No longer considered a true fissural cyst. AVOID USING THIS TERM
-Age/Sex: Adults M=F
-Clinical: swelling between maxillary lateral and cuspid. Roots are spread and there is a circumscibed radiolucency resembling an inverted pear
Globulomaxillary Cyst Histology, Treatment, Prognosis
-Histology: Lesion most often has the histology of one of the following: lateral radicular cyst, lateral periodontal cyst, OKC
-Treatment: complete removal
-Prognosis: Good, recurrence not unusual historically a developmental cyst but pathologically most like a primordial cyst
Nasolabial Cyst Age/Sex, Clinical
-aka Nasoalveolar cyst, Klestadt's cyst
-may arise from remnants of nasolacrimal duct or from fusion of maxillary medial nasal and lateral nasal processes
-Age/Sex: Adults, F>M by 3:1
-Clinical: soft tissue swelling in nasolabial fold, may elevate fold, may elevate floor of nostril. Radiograph shows occasional shadow (ill defined radiolucency) over area
Nasolabial Cyst Histology, Treatment, Prognosis
-Histology: Cyst lined by respiratory epithelium rimmed by inflamed fibrous connective tissue
-Treatment : complete removal via an intraoral approach , may be necessary to sacrifice a portion of the nasal mucosa
-Prognosis: Good
Oral Lymphoepithelial cyst Age/Sex, Clinical
-Age/Sex: Young adults
-Clinical: soft small .5-1cm, yellow, rounded, subepithelial mass in floor of mouth or in Waldeyer's ring
Oral Lymphoepithelial cyst Histology, treatment, prognosis
-Histology: Cystic Space usually filled with keratin rimmed by stratified squamous epithelium, surrounded by lymphoid tissue
-Treatment: conservative surgical removal
-Prognosis: excellent
Branchial Cleft cyst Age/Sex, Clinical
-aka lymphoepithelial cyst
-Age/Sex: young adults, ages 20-24
-Clinical: soft circumscribed swelling, 1-2cm in diameter in cervical chain, close to anterior border of SCM muscle. May be also seen in submandibular and parotid region
Branchial Cleft Cyst Histology, treatment, prognosis
-Histology: Cyst lined by stratified squamous epithelium or columnar epithelium surrounded by lymphoid tissue
-Treatment: Surgical removal with node
-Prognosis: Good, but there is a question of malignant potential of epithelium
Thyroglossal duct cyst Age/Sex, Clinical
-Age/Sex: most common in the first two decades of life
-Clinical: fluctuant, movable mass in midline of anterior neck. Elevates on swallowing or protruding of tongue. May be seen from base of tongue to base of neck. Size about 3cm. If high in neck or in tongue may cause dysphagia or choking. fi in lower neck draining sinus may be found in skin.
Thyroglossal duct cyst Histology, Treatment, prognosis
-Histology: Cyst lined by stratified squamous epithelium or columnar epithelium. In fibrous connective tissue wall, thyroid tissue may be seen.
-Treatment: Surgical removal via Sistrunk procedure
-Prognosis: good
Sistrunk Procedure
-for removal of thyroglossal duct cysts
-Cyst is remove in addition to the midline segment of the hyoid bone, and a generous portion of the muscular tissue along the entire thyroglossal tract
Aneurysmal Bone cyst Age/Sex, Clinical
-Age/Sex: <20 years, F>M
-Clinical: Mandible>maxilla; expansile, painless with radiolucency which may be soap bubble like, Blow out disention of contour of affected bone
Aneurysmal bone cyst Histology, Treatment, prognosis
-Histology: pools of blood rimmed by immature connective tissue containing giant cells, bone, hemosiderin. May be associated with other benign lesions
-Treatment: conservative complete surgical removal
-Prognosis: moderate, recurrence rates as high as 50%
Traumatic bone cyst Age/Sex, Clinical
-Aka univameral bone cyst, solitary bone cyst, simple bone cyst, hemorrhagic bone cyst
-Controversial etiology, trauma that doesnt cause fracture results in intraosseous hematoma which may liquefy and cause a cystic defect
-Age/Sex: <25 years, M>F
-Clinical: usually painless with unicystic radiolucency scalloping around tooth roots, mandible most often
Traumatic bone cyst histology, treatment, prognosis
-Histology : no epithelium, granulation tissue, viable bone
-Treatment: open surgically create fresh hemorrhage then close
-Prognosis: Good
Stafne Bone cyst Age/Sex, Clinical
-aka static bone cyst, lingual mandibular salivary gland depression
-Age/Sex: Adults, 80-90% of cases in males
-Clinical: asymptomatic sharply defined radiolucency usually in posterior mandible below the mandibular canal. Linugal cortex of mandible missing
Stafne Bone Cyst Histology, treatment, prognosis
-Histology: when surgically explored these reveal salivary gland or loose connective tisse
-Treatment: None; radiographic diagnosis is sufficient. Anterior lesions may be biopsied to r/o other pathoses
-Prognosis: excellent
Mucocele Age/Sex, Clinical
-aka mucous extravasation or retention phenomenon
-Age: any age; usually children and young adults. Most common swelling of lower lip
-Clinical: Most common location- lower lip but also on cheek tongue palate (very, rarely on upper lip) due to trauma to salivary gland duct. Are raised soft, painless translucent-often regress in size only to re-enlarge. Also occur in sinus. May appear translucent and bluish if superficial
Mucocele Histology, Treatment, Prognosis
-Histology: Cyst like space containing mucus and inflammatory cells, rimmed by granulation tissue . Salivary gland noted at base
-Treatment: surgical excision to include underlying salivary gland. In sinus (umbrella cyst) no treatment, as lesions regress spontaneously
-Prognosis: good, recurrence unlikely if associated gland is also removed
Ranula Age/Sex, Clinical
-aka retention cyst
-usually due to mucus spillage from the sublingual glands.
-Age/Sex any age, M=F
-Clinical: Associated with submandibular or sublingual glands Larger than mucocele in floor of mouth. Lies laeral to midline. When superficial, has bluish hue (like frod belly) but may be deep and penetrate mylohyoid muscle (plunging ranula)
Ranular Histology, Treatment, Prognosis
-Histology: similar to mucocele, deep or plunging ranula may appear like granulation tisue with many macrophages
-Treatment: complete excision but may marsupialize
-Prognosis: good, recurrrence rate is high with tx. by marzupialization
Dental granuloma Age/Sex, Clinical
-aka periapical granuloma
-Age/Sex: any age, M=F
-Clinical: same as radicular cyst
Dental Granuloma Histology, treatment and prognosis
-Histology: immature fibrous connective tissue with dense infiltrate of chronic inflammatory cells
-Treatment: Endodontic therapy
-Prognosis: good
Apical Scar Age/Sex, Clinical
-Age/Sex: Adults, M=F
-Clinical: Endodontically treated tooth with periapical surgery which has perforated and destroyed periosteum.Otherwise asymptomatic
Apical Scar Histology, treatment, prognosis
-Histology: Scar tissue
-treatment: none
-Prognosis: good
Types of odontogenic tumors
-Ameloblastoma
-malignant ameoloblastoma
-ameloblastic carcinoma
-Pindborg tumor
-Squamous odontogenic tumor
-clear cell odontogenic tumor
Ameoloblastoma age/sex, clinical, signs symptoms
- aka plexiform, acanthomatous, follicular, basaloid, granular subtypes)
-age/sex: 20-70 years,
-Clinical: mandible 85%: 3/4 in posterior,a unilocular or multilocular radiolucency
-Signs/Symptoms: painless; swelling
Ameloblastoma Histology, treatment, prognosis
-histology: strands, cords, sheets, islands of odontogenic epithelium showing features noted below: loosely arranged epithelial cells resembling the stellate reticulum of the enamel organ. Columnar peripheral cells resembling ameloblasts with reverse polarity of their nuclei
-treatment: wide excision
-Prognosis: fair to good
Unicystic Ameloblastoma Age/Sex, Clinical, Signs/symptoms
-age/sex: 10-30yrs, either sex
-Clinical: mandibular molar region, unilocular radiolucency
-signs/symptoms: failure of tooth eruption and discovery of pericoronal radiolucency
Unicystic ameoloblastoma histology, treatment, prognosis
-Histology: cystic lesion has rimming epthelium showing: a columnar epithelium with hyperchromatic nuclei and reveral of nuclear polarity; hyperplasia of cystic lining wtih loss of epithelial cohesion; budding of epithelium into adjacent connective tissue
Treatment: Curettage
-prognosis: good, rate of recurrence <20%
Malignant Ameloblastoma Age/Sex, Clinical, Signs/Symptoms
-Age/sex: 4-75yrs
-Clinical: lungs, may be seen on chest x-ray
-Signs/symptoms: often a symptomatic
Malignant Ameloblastoma histology, treatment, prognosis
-Histology: identical to benign jaw lesion
-treatment: wide excision
-Prognosis: guarded, 50% die of disease
Ameloblastic Carcinoma age/sex, clinical, signs/symptoms
-Age/Sex: 6th decade
-Clinical: mandible>maxilla, irregular jaw destruction
-signs/symptoms: Rapid jaw expansion
Ameloblastic Carcinoma Histology, treatment
-Histology: microscopic features of ameloblastoma and cytologic features of malignancy
-treatment: surgery, radiation, chemotherapy, similar to SCC
Pindborg Tumor age/sex, clinical, signs/symptoms
-aka CEOT, calcifying epithelial odontogenic tumor
-age/sex, 30-50yrs
-Clinical: posterior mandible, frequently associated with crown of impacted tooth. Loculated radiolucency with strands of calcifications of varying amounts
-Sign/symptoms: painless; swelling
Pindborg Tumor Histology, treatment, prognosis
-Histology: pleomorphic odontogenic epithelium, desmosomes, amyloid and calcification
-treatment: conservative surgical removal
-Prognosis : good
Squamous odontogenic tumor age/sex, clinical, signs/symptoms
-age/sex: 10-70yrs
-Clinical: throughout mandible and maxilla. may involve multiple sites most often. Triangular or semicircular radiolucencies with sclerotic borders associated with cervical portion of tooth root.
-Signs/symptoms: probably arises from rest of Malassez in periodontal ligament tooth mobility, vague pain; teeth sensitive to percussion
Sqaumous odontogenic tumor histology, treatment, prognosis
-Histology: islands of mature squamous epithelium without atypia, mature collagenized fibrous connective tissue stroma, foci of calcification of the epithelium, hyalinized eosinophilic structures
-Treatment: conservative surgical removal, maxillary lesions may be more widespread
-prognosis: good
Clear Cell odontogenic tumor age/sex, clinical, signs/symptoms
-Age/Sex: >50yrs
-Clinical: either jaw, unilocular or multilocular radiolucencies
-signs/symptoms: some complain of pain and swelling. Others are symptom free
Clear cell odontogenic tumor histology, treatment, signs/symptoms
-histology: nests of epithelial cells with clear cytoplasm separated by thin strands of hyalinized connective tissue
-treatment: radical surgery, work-up for metastatic disease
-prognosis: fair
Types of mixed Epithelial-mesenchymal tumors
-adenomatoid odontogenic tumor
-odontoma comound
-odontoma complex
-ameloblastic fibroma
-ameloblastic fibro-odontoma
-ameloblastic fibrosarcoma
Types of odontogenic ectomesenchyme tumors
-odontogenic fibroma
-granular cell odontongenic tumor
-odontogenic myxoma
-benign cementoblastoma
Adenomatoid Odontogenic Tumor age/sex, clinical, signs/symptoms
-aka AOT, OAT
-age/sex: <30yrs
-clinical anterior maxilla most often, circumscribed radiolucency around crown of impacted canine
-signs/symptoms: asymptomatic radiolucency
Adenomatoid odontogenic tumor histology, treatment, prognosis
-histology: whorled masses of odontogenic epithelium that form rosette-like or duct like structures. Nuclei are polarized away from the center of the duct. foci of calcification are observed.
-treatment: conservative surgical removal
-prognosis: excellent
Odontoma Compound age/sex, clinical, signs/symptoms
-age/sex: 10-20yrs
-clinical: anterior maxilla most often. usually <1cm tooth like radiopacity in tooth-bearing area
-Signs/symptoms: asymmetry in eruption pattern most often
Odontoma compound histology, treatment, prognosis
-histology: regular enamel, dentin, pulp, cementum
-treatment: conservative surgical removal
-prognosis; excellent
Odontoma Complex age/sex, clinical, signs/symptoms
-Age/sex: 10-20 yrs
-clinical: posterior mandible most often, irregular radiodensity
-signs/symptoms: eruption asymmetry
Odontoma Complex histology, treatment, prognosis
-histology: haphazard deposition of enamel, dentin,etc
-treatment: conservative surgical removal
-prognosis: excellent
Ameloblastic Fibroma age/sex, clinical, signs/symptoms
-aka soft odontoma
-Age/sex: <20yrs
-clinical: mandible, premolar/molar, circumscribed radiolucency
-signs/symptoms: painless swelling
Ameloblastic Fibroma histology, treatment, prognosis
-histology: pulp-like stroma with islands of ameloblastic epithelium
-treatment: complete surgical removal
-Prognosis: recurrence frequent
Ameloblastic Fibro-odontoma age/sex, clinical, signs/symptoms
-age/sex: <20yrs
-clinical: mand<maxilla, posterior jaw , circumscribd radiolucency containing radiopacity with crown of tooth
-signs/symptoms: slow growing asymmetry in eruption
Ameloblastic fibro-odontoma histology, treatment, prognosis
-histology: ameloblastic fibroma+odontoma
-treatment: complete surgical removal
-prognosis: good
Ameloblastic fibrosarcoma age/sex, clinical,signs/symptoms
-age/sex: M>F
-Clinical 80% in mandible, ill-defined destructive radiolucency
-signs/symptoms: pain + swelling with rapid clinical growth
Ameloblastic fibrosarcoma histology, treatment, prognosis
-histology: epithelial component like ameloblastic fibroma, mesenchymal component is cellular and pleomorphic with mitoses
-Treatment: radical surgical excision
-prognosis: guarded/
Types of Tumors of Odontogenic Ectomesenchyme
-odontogenic fibroma (simple type, WHO type Peripheral odontogenic fibroma
-granular cell odontogenic tumor
-odontogenic myxoma (myxoma, myxofibroma)
-Benign Cementoblastoma
Odontogenic Fibroma Age/sex clinical, signs/symptoms
-has a simple and a WHO type peripheral odontogenic fibroma (soft tissue counterpart)
-Age/sex 4-80 yrs
-Clinical: located in posterior mandibular = anterior maxilla, circumscribed radiolucency. WHO type may have radiopaque flecks.
-Signs/symptoms: painless, slow growth in bone
Odontogenic Fibroma histology, treatment, prognosis
-fibrous connective tissue with evenly spaced cuneiform cells
-WHO type has more prominent odontogenic epithelial rests and calcifications
-treatment: enucleation and curettage
-prognosis: good
Granular Cell Odontogenic tumor Age/sex, clinical, signs/symptoms
-age/sex: adults
-Clinical: located in premolar/molar region of mandible. Radiographically circumscribed radiolucency occasional calcifications
-Signs/Symptoms: asymptomatic radiolucency, occasional calcifications
Granular Cell odontogenic histology, treatment, prognosis
-histology: islands of odontogenic epithelium scattered among granular cells
-Treatment: curettage
-prognosis: good
Odontogenic Myxoma Age/sex, clinical, signs/symptoms
-aka myxoma, myxofibroma
-age/sex 50% between 10-30 yrs; rarely >50 yrs
-Clinical: located posterior of jaws; mandible=maxilla, circumscribed radiolucency uni or multilocular
Odontogenic Myxoma histology, treatment, prognosis
-histology: pulp-like juicy mucoid
-treatment surgery with cautery
-prognosis: good by 25% recurrence
Benign Cementoblastoma age/sex, clinical, signs/symptoms
-aka true tumor of cementum
-age/sex: 10-25 yrs
-clinical : located in mandible, molar-premolar region. circular radiolucency containing round radiopacity; eroding tooth roots
-signs/symptoms: swelling with or without pain
Benign Cemtoblastoma histology, treatment, prognosis
-histology: cellular, vascular stoma+ cementum
-treatment: surgical removal, usually involves extraction of the involved tooth
-prognosis: good but follow
Papilloma age/sex, clinical
-age/sex: 30-50 yrs, M=F
-Clinical: caused by human papillomavirus cauliflower-like exophytic painless, non indurated, soft variable duratio. Location: palate uvula, tongue, lip gingiva, buccal mucosa, floor of mouth; multiple in 4% of cases. Color varies with location: from keratinized surface-white from non-keratinized surface- red/pink. Large lesions, >2 cm, should consider condyloma acuminatum (HIV a consideration)
Papilloma histology, treatment, prognosis
-histology: papillary lesion of stratified squamous epithelium may be keratinized may see mitoses, supporting core of immature vascular fibrous connective tissue, similar to verruca vulgaris
-treatment: excision at base
-prognosis: excellent
Verruca Vulgaris age/sex, clinical
- aka common wart
-caused by HPV 2, 4, 40
-age/sex: any age, but frequent in children, M=F
-Clinical: caused by HPV, exophytic sessile, white, painless, non-indurated, usually <6 months duration. Search for other lesions on skin of fingers, etc.
Verruca Vulgaris Histology, treatment, prognosis
-histology: cauliflower like covered by keratotic stratified squamous epithelium; constricted at the base by a collarette.
-treatment: excision may even spontaneously regress
-prognosis: excellent
Condyloma acuminatum age/sex, clinical
-Caused by HPV 6,11,16,18
-age/sex: usually in teenagers and young adults. M>F
-clinical: sexually transmitted. appearance similar to papilloma
Condyloma acuminatum histology, treatment, prognosis
-Histology: similar to papilloma, may be larger and multiple
-Treatment: excision
-prognosis: recurrence common
Focal epithelial hyperplasia age/sex, clinical
- aka Heck's disease
-caused by HPV 13, 32
-age/sex: more often in childhood, M=F
-Clinical: multiple cauliflower-like lesions found in ppl living in crowded unsanitary conditions
Focal epithelial hyperplasia histology, treatment, prognosis
-histology: no hyperkeratosis, mitotic/mitosoid figures in spinous layer of epithelium
-treatment: excision may regress
-prognosis: excellent
Verruciform Xanthoma age/sex, clinical
- adult: 40-70 yrs, F>M by 2:1
-clinical: slightly raised, soft pebbly surfaced; <1.5cm; asymptomatic; white, yellow/white;red;pink. Most often on gingiva and alveolar ridge. Idiopathic
Verruciform Xanthoma histology, treatment, prognosis
-Histology: covered by warty keratinized stratified squamous epithelial; underlying connective tissue contains large foamy cells lying just beneath epithelium
-treatment: excision
-prognosis: excellent
Types of benign oral epithelial lesions
-papilloma
-verruca vulgaris
-condyloma acuminatum
-focal epithelial hyperplasia
-verruciform xanthoma
-oral melanotic macule
-melanocytic nevus
-keratocanthoma
Oral melanotic macule age/sex, clinical
-aka focal melanosis
-age/sex: F>M by 2:1, average age=43
-clinical: solitary oval lesion <7mm, vermillion border, buccal mucosa, gingiva, palate
Oral melanotic macule histology, treatment, prognosis
-histology: increased melanin in basal layer. Epithelium is normal. Melanin incontinence (melanophages in upper connective tissue)
-treatment: prophylactic excision
-prognosis: good
Melanocytic nevus age/sex, clinical
-aka nevocelluar nevus; mole
-age/sex: begins to develop in childhood and most are present before age 35. Involution in elderly
-clinical: localized pigmented brown to dark blue to black, flat or slightly raised, painless, static lesions, usually on palate maxillary gingiva
Melanocytic nevus histology, treatment, prognosis:
-histology: presence of small rounded cells with benign nuclei and variable amounts of melanin in cytoplasm lying singly or in theques (clusters) either at basal lamina (junctional nevus) or in underlying connective tissue (intramucosa) or both locations (compound) may present spindle shaped cells (blue nevi)
-treatment: prophylactic excision
-prognosis: good
Keratocanthoma age/sex, clinical
-aka: pseudoepitheliomatous hyperplasia (P.E.H)
-caused by HPV 26 or 37?
-age/sex: >45 years; M>X, 3:1
-clinical: rapidly growing (4-8 weeks), crusting nodule, 1-2cm in diameter, keratin-filled core, painless, usually on lip, will spontaneously regress with scarring
Keratocanthoma histology, treatment, prognosis
-histology: hyperparakeratotic stratified squamous epithelium, elevated at periphery with broad epithelial bands growing downward; margins at surface are constricted at surface are constricted in ice-tong effect cellular atypia noted; subepithelial chronic inflammation
-treatment: complete excision
-prognosis: good
Types of Premalignant and malignant epithelial neoplasms
-leukoplakia
-erythroplakia
- carcinoma in situ
-squamous cell carcinoma
-verrucous carcinoma
-proliferative verrucous leukoplakia
-basal cell carcinoma
-melanoma
Leukoplakia age/sex, risk factors
-a white plaque that doesnt wipe off and not recognizable as any other disease
-age/sex: > age 40, M>F
-risk/factors: tobacco usage and EtOH abuse increase risk of malignancy
Leukoplakia histology, treatment, prognosis
-histology: hyperorthokeratosis, hyperparakeratosis, acanthosis in most cases. dysplasia ; irregular epithelial maturation (loss of polarity, altered nuclear/cytoplasmic, ratios, pleomorphism, enlarged nucleoli, hyperchromatic nuclei, drop-shaped (bulbous) rete ridges.
-treatment: surgical removal
-prognosis: good tempered by side, change of habits, if untreated, 4% progress to cancer
Erythroplakia age/sex, risk factors
-erythroplasia (red plaquethat is not recognizable as any other disease, three types: homogenous, mixed speckled; granular
-age/sex: peak prevalence 65-74. M>F
-risk factors: locations; most often floor of mouth, ventral tongue, lower lip, palate, retromolar area
Erythroplakia histology, treatment, prognosis
-histology: 91% are dysplastic! See leukoplakia
-treatment: surgical removal
-prognosis: guarded., follow patient closely e.g. every 6 months
Carcinoma in situ age/sex, risk factors
-aka Bowen's disease, CIS, squamous cell CA grade 1/2
-A histologic diagnosis
-age/sex: M>F but sexual predominance decreasing
-risk factors: locations as above, tobacco and alcohol abuse contributory
Carcinoma in site histology, treatment, prognosis
-histology: marked dysplasia through entire thickness of mucosa but not yet invading
-treatment: surgical removal
-prognosis: guarded. Follow patient very closely, e.g every 3 months
Squamous Cell carcinoma age/sex., risk factors
-aka epidermoid carcinoma
-age/sex: usually >40 age group, M>F, but sexual predominance decreasing
-risks: tobacco, EtOH-synergizes with tobacco to create greater risk. Sunlight. Location floor of mouth, lateral tongue, lower lip
Squamous cell carcinoma histology, treatment, prognosis
-histology: microscopic features of dysplasia plus invasion of underlying lamina propria
-treatment: surgical removal, radiation, or chemotherapy
-prognosis: guarded; depending on location, lesion size, tempered by habit change
Verrucous carcinoma age/sex, risk factors
-aka Snuff Dipper's carcinoma
->55 years of age. Predominantly in males
-risk factors: directly related to snuff or chewing tobacco. Location: mucobuccal fold; alveolar ridge; palate
Verrucous Carcinoma histology, treatment, prognosis
-histology: exophytic, well differentiated, keratinized. Superficially invasive. Little dysplasia
-treatment: surgical removal preferred to radiation treatment
-prognosis: good if completely removed
Proliferative Verrucous leukoplakia age/sex, risk factors
-progressive clinical condition eventuating in SCC
-age/sex: F>M
-risk factor: tobacco may be a factor
Proliferative Verrucous leukoplakia histology, treatment, prognosis
-histology: varies from grade 1 through verroucous carcinoma, to papillary squamous cell carcinoma, to less differentiated squamous carcinoma
-treatment: surgery radiation
-prognosis: guarded; many die of the condition
Basal Cell Carcinoma age/sex, risk factors
-aka basal cell epithelioma
-age/sex: skin of adults;slowly enlarging long-standing ulcer
-risk factor: fair complexion, exposure to strong sunlight, sun-exposed skin of mid-face, upper>lower lip
Basal Cell Carcinoma histology, treatment, prognosis
-histology: invasive strands, islands of epithelium, peripheral cells columnar like basal layer of mucosa, inner cells polyhedral. Stroma proliferates with tumor in strands parallel to tumor surface
-treatment: eradicate lesions by surgery, cautery, radiation, cryotherapy
-prognosis: good
Melanoma age/sex, risk factors
-4 types: lentigo maligna, superficial spreading, nodular, acral lentiginous
-age/sex: 30-80 years of age. Increased risk associated with family history and increased sun exposure.
-risk factors: Long-standing pigmented spot (1-5 years). A,B,C,D. May be difficult to distinguish between other pigmentations and melanoma
Melanoma histology, treatment, prognosis
-histology: melanocytes growing toward 1 surface as well as penetrating deeply. Cellular atypia. Abnormal mitoses, lymphocytic infiltrate present
-treatment: aggressive surgery, supplemental immunotherapy
-prognosis: poor especially for intraoral lesions
Types of Benign mesenchymal oral lesions
-fibroma
-giant cell fibroma
-lipoma
-granular cell tumor
-congenital epulis of the newborn
-neurofibroma
-neurilemoma
-multiple mucosal neuroma syndrome
Fibroma age/sex, clinical
-aka focal fibrous hyperplasia, traumatic or irritation fibroma
-age/sex: any age, either sex
-clinical: firm, pink, exophytic nodule, found on tungue and cheek, most often but can be on any mucosal site of trauma
Fibroma histology, treatment, prognosis
-histology: tumor of densely collagenized fibrous connective tissue; moderately vascularized; little inflammation; covered by stratified squamous epithelium
-treatment: surgical removal
-prognosis: no recurrence if trauma is eliminated
Giant Cell fibroma age/sex, clinical
-Age/sex: any age, either sex
-clinical: soft pink, exophytic on gingiva, palate, lip tongue
Giant Cell Fibroma histology, treatment, prognosis
-histology: elevated mass of moderately collagenized fibrous connectivetissue with single or multi-nucleated fibroblasts showing a stellate appearance. Little inflammation . Covered by stratified squamous epithelium
-treatment: surgical removal
-prognosis: no recurrence
Lipoma age/sex, clinical
-age/sex: any age
-clinical: soft, light yellow (when superficial in loaction), non-ulcerated, painless, evenly rounded, raised mass, static or slowly growing, in cheek, tongue, floor of mouth; delicate smooth covering that exhibits small vessels
Lipoma histology, treatment, prognosis
-histology: lobules of mature fat in a loos fibrous stroma, a little inflammation; floats in fixative
-treatment: surgical removal
-prognosis: good
Granular cell tumor age/sex, clinical
-aka granular cell myoblastoma, granular cell schwannoma, granular cell neurofibroma
-age/sex: any age; 2:1 female pedilection
-clincial: slightly raised, non-ulcerated; small (<2cm), painless, firm nodules of varying duration; tongue most often, but also on palate, lips, gingiva
Granular cell tumor histology, treatment, Prognosis
-histology: fibrous connective tissue containing nests of large cells with granular cytoplasm prominent cell membranes and centrally placed, benign nuclei; covering stratified squamous epithelium may be hyperplastic; simulating squamous cell carcinoma (P.E.H)
-treatment: surgical removal
-prognosis: good
Congenital Epulis of the newborn age/sex, clinical
-aka congenital gingival granular cell tumor
- age/sex: newborn, female predilection
- clinical: maxillary gingiva > mandibular, 4:1 soft rounded, exophytic, non-ulcerated mass attached to alveolar ridge
Congenital Epulis of the newborn histology, treatment, prognosis
-histology: sheets of cells exactly like granular cells above with little stroma, no epithelial hyperplasia. S-100 negative
-treatment: surgical removal
-prognosis: good
Neurofibroma age/sex, clinical
-look for multiple lesions, consider von-recklinghausen's disease
-age/sex: solitary tumors most common in young adults
-clinical: firm solitary or multiple nodules, variable sized usually painless non ulcerated located on tongue most often, but no site immune, look for multiple lesions and cafe au lait spots on skin
Neurfibroma histology, treatment, prognosis
-histology: localized mass of interlacing Schwann cells and perineural fibroblasts that have spindled, round or comma shapes
-treatment: surgical removal
-prognosis: if V-R, disease is progressive with malignant potential
Neurilemoma age/sex, clinical
-aka Schwannoma
-age/sex: any age, but usually adults
-clinical: circumscribed firm nodule non-ulcerated usually painless, location, tongue most often but any location. Presents as circumscribed firm mass
Neurilemoma histology, treatment, prognosis
-histology: circumscribed mass with same microscopy as above (Antoni B tissue) plus oranoid collections of Schwann cells with solid center (verocay bodies/Antoni A tissue
-treatment: surgical removal
-prognosis: good
Multiple mucosal neuroma syndrome age/sex, clinical
-aka M.E.N III
- age/sex: young, neuromas may present by age 5
-clinical: tall persons with multiple nodules on anterior tongue, just below commissures of lips, cheeks, gingiva; painless, static, non-ulcerated
Multiple Mucosal neuroma syndrome histology, treatment, prognosis
-histology: neuromas with prominent perineurium, ganglion cells present
-treatment: remove thyroid or monitor calcitonin levels
-prognosis: carefully evaluate for pheochromocytoma, medullary carcinoma
Sarcoma
-a malignancy of connective tissue origin
-differs from a carcinoma by its mode of metastasis and growth rate
Types of soft tissue sarcomas
-fibrosarcoma
-fibrous histiocytoma
-liposarcoma
-neurofibrosarcoma
-angiosarcoma
-Kaposi sarcoma
-Leiomyosarcoma
-Rhabdomyosarcoma
Fibrosarcoma
-malignancy of fibroblasts
-young adults and children
-true fibrosarcomas are uncommon in the oral cavity
Fibrous histiocytoma
-malignancy with fibroblastic and histiocytic differentiation
-The most common soft tissue sarcoma in adults
-most common site : extremities
-rare in the head and neck
-very aggressive, high recurrence and metastatic rate
Liposarcoma
-malignancy of adipose tissue
-second most common soft tissue sarcoma of adults
-rare in the head and neck (neck is more common site)
-peak age group: 40-60
Neurofibrosarcoma
-principal malignancy of nerve sheath origin
-50% occur in patients with neurofibromatosis
-5 year survival rate with patients with neurofibromatosis is only 16%, for other it is 53%
Angiosarcoma
-a rare malignancy of vascular endothelium
-scalp and forehead are the most common head and neck sites
Kaposi Sarcoma Etiology
-propensity to develop in HIV+ individuals
-multicentricity
-geographic distribution
-patient population suggests a viral origin
-Human herpes virus -8 has been suggested as the most likely virus
-lesion most likely arises from endothelial cells with some evidence of lymphatic origin
Kaposi Sarcoma Clinical types
-classic: elderly jewish, slavic or italian males on lower extremities
-Endemic : african
-Iatrogenic Immunosuppression associated
-AIDS related
Kaposi Sarcoma Histopath Stages
-patch: proliferation of miniature vessels
-plaque: proliferation of vessels with spindle cells
-nodular: increased spindle cells to make a nodular tumor mass containing extravasated erythrocytes
Kaposi Sarcoma treatment
-systemic vinblastine
-intralesional vinblastine
-laser surgery
Leiomyosarcoma
-malignancy of smooth muscle cells
-middle aged to older adults
-rare in the oral cavity
Rhabdomyosarcoma
-the most common soft tissue sarcoma in children
-primarily occurs in first decade, 60% in males
-rapidly growing, painless infiltrating mass
-orbit>nasal cavity>nasopharynx
-palate=most frequent intraoral site
-in recent years the advent of multimodal chemotherapy has improved the prognosis drastically
Oral cancer epidemiology
-roughly 1,000,000 cases of new cancers are diagnosed annually in the US
-3-4% are cancers of the oral cavity and oropharynx
-if hypopharynx, nasopharynx, sinuses and major salivary glands are included--- 5%
-Cancer will develop in 1 person in every 4 and in two families of every three
-Between 57-60 million Americans now living will someday have cancer
Oral Cancer Statistics
-91% of oral malignancies are squamous cell carcinoma
-average age: >60
-more than 1/3 of americans are over 45
-the older age of oral cancer patients suggests that a time factor may be operating which involves predetermined processes in biochem/physio. of aging cells
-biologic processes include: DNA repair activity, enzymatic changes, metabolic factors, immunologic factors
-processes influenced by: chemicals, viruses, hormones, nutrients, physical irritants
Predilections to oral cancer
-site: posterior lateral tongue, lip cancer is down, possibly due to sunscreens
-sex: greater in males, ratios are changing though, was 6 male: 1 female in 1950, now 2 male: 1 female
-increase in smoking in women in last 20-30 yrs, age may also play some role
-over age 65, women exceed men by 45%
Metastasis oral cancer
-78% of posterior 1/3 tongue lesions had regional metastases at time of diagnosis
-the more posterior the lesion, the more likely metastasis is to occur
Etiology and Predisposing Factors for cancer
-immune competence and surveillance: down with age (older people are more likely to get cancer)
-additional problems which increase the likelihood of cancer (congenitally defective immune system, AIDS, radiation/chemotherapy)
-tobacco
-smokeless tobacco
-india
-genetics and ethnicity
Tobacco
-aromatic hydrocarbons(tars) are the most important carcinogens
-Nicotine: the habituating substance in tobacco
-filters can decrease harmful substances, but studies have shown them to be associated with increased smoking
-federal law requires 4 warnings to be rotated on cigarette packages
Federal Warnings on Cigarette packages: Surgeon General's Warning
- smoking causes lung cancer, heart disease, emphysema, and may complicate pregnancy
-Quitting smoking now greatly reduces serious risk to your health
-smoking by pregnant women may result in fetal injury, premature birth and lo birth weight
-cigarette smoke contains carbon monoxide
Smokeless tobacco
-question of threat for increased oral cancer in the future
-NC case study showed 50X the risk for cancer of the gingiva and buccal mucosa in habitual snuff dippers
India (Risk and predisposing factor to cancer)
-highest rate of oral cancer in the world
-50-65% of all cancers in this country are oral cancers
-different habits: use of betel nuts, slaked lime and spices in their tobacco
-reverse smoking- increased palatal cancer
Genetics and Ethnicity
-cancer in american blacks has increased at a greater rate than whites
-blacks have increased rates of oropharyngeal cancer compared to other racial groups
-cancer in nasopharynx: 20-30X more prevalent in chinese than whites (EBV association)
Field cancerization phenomenon
-if you've had one oral malignancy, your chances are greatly increased for another especially if your tobacco habits remained unchanged
Morality (cancer)
-death rate from cancer has risen uninterrupted for the past 6 decades
-oral cancer - 10,000 deaths yearly (2.2% of total)
-increased death rate of black males twice that of white males during the past 2 decades
-socioeconomic?, smoking/alcohol patterns?
AIDS related oral malignancies
-Kaposi's Sarcoma
-Squamous cell carcinoma
-Burkitt's Lymphoma
Malignant Pleomorphic Adenoma age/sex, clinical
-adenocarcinoma arising in pleomorphic adenoma malignant mixed tumor
-age/sex: >60's; F>M
-clinical: 7% long standing pleomorphic adenoma, sudden spurt of growth and pain
Malignant Pleomorphic Adenoma pathology, treatment, prognosis
-Pathology: pleomorphic adeonma plus area with malignant features eroding capsule
-treatment: aggressive surgery
-prognosis: guarded, 50% survive 2-3 years
Low Grade Mucoepidermoid Carcinoma age/sex, clinical
-aka mucoepidermoid tumor
-age/sex: adults M=F
-Clinical: slowly growing, painless, soft mass, may appear like a mucocele
Low Grade Mucoepidermoid Carcinoma pathology, treatment, prognosis
- pathology: four cell types: squamous epithelium, mucous cells, intermediate cells, clear cells
-treatment: complete surgical removal
-prognosis: good 90% survive 5 years
High Grade Mucoepidermoid Carcinoma age/sex, clinical
-age/sex: adults, M=F
-clinical: painful rapidly growing aggressive
High Grade Mucoepidermoid Carcinoma pathology, treatment, prognosis
-pathology: solid, cellular pleomorphism, squamous predominant, spreading widely
-treatment : aggressive surgery
-prognosis: poor; <10% survive 5 years
Adenoid Cystic Carcinoma age/sex, clinical
-aka adeonocystic carcinoma, cylindroma
-age/sex: 40-60 yrs, F>M
-clinical: palate, most common site; slowly growing, painful may be ulcerated may be freely movable
Adenoid Cystic Carcinoma pathology, treatment, prognosis
-pathology: small, uniform, basaloid cells, in a "cribform" or "swiss cheese" pattern involves nerves; may be solid; stroma may be hyalinezed; eosinophilic pools in cystic spaces
-treatment: aggressive surgery
-prognosis: short term good, long term poor
Terminal Duct Cell carcinoma age/sex, clinical
-aka polymorphous low grade adenocarcinoma
-age/sex: M=F, older adults
-clinical: always in intraoral, minor salivary glands
Terminal Duct Cell Carcinoma pathology, treatment, prognosis
-pathology: localized sheets of cells in middle of tumor with strands at periphery; larger cells, prominent cytoplasm; around nerves
-treatment: complete removal
-prognosis: good <10% metastasize
Acinic cell carcinoma age/sex, clinical
-age/sex: adults in 40's, F>M 2-3:1
-clinical: 2.5% in major glands; principally parotid; a long-standing " lump" usually painless
Acinic Cell Carcinoma pathology, treatment, prognosis
-pathology: serous cells with granular cytoplasm, clear cells in masses, lobules, small and large cystic spaces
-treatment: surgery
-prognosis: good but follow; 20 year survival 50%
Adeno-Carcinoma Carcinoma age/sex, clinical
-age/sex: adults in 60's , F>M
-clinical: 10% of salivary gland tumors; pain, poorly defined, rapidly growing of short duration
Adeno-carcinoma Carcinoma pathology, treatment, prognosis
-pathology: Sheets masses of anaplastic cells of ductal origin, ducts may be found
-treatment: aggressive surgery
-prognosis: poor