Dysplasia and Oral Cancer Flashcards

1
Q

What are the 2 distinct disease patterns

A

Oral Cavity Cancer (OCC)

Oro-Pharyngeal Cancer (OPC)

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2
Q

What are the high risk sites for mouth cancer

A

Floor of the mouth

Lateral border of the tongue

Retromolar regions

Soft and hard palate

Gingivae

Buccal mucosa

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3
Q

What is the risk for smokers who dont drink

A

x2 risk

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4
Q

What is the risk for drinkers who dont smoke

A

x2

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5
Q

What is the risk for those who smoke and drink

A

x5

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6
Q

What is the risk for those who take Betel quid

A

x3 risk

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7
Q

What else can increase your risk of oral cancer

A

Family history

Oral health

Sexual activity

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8
Q

What are the potentially malignant lesions

A

White lesions (leukoplakia)

Red lesions (erythroplakia)

Lichen planus
-Candidal Leukoplakia
-Chronic Hyperplastic Candidiasis

Oral Submucous Fibrosis

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9
Q

What is the incidence of oral cancer in white lesions

A

0.2-4% incidence

Malignant change= 2.5% in 10 years, 4% in 20 years

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10
Q

What is the cancer risk for Erythroplakia

A

much less frequent than leukoplakia

much higher risk of cancer

greater dysplasia risk
-Up to 50% already be carcinoma

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11
Q

What is dysplasia

A

the abnormal development of cells within tissues or organs

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12
Q

What is dysplasia based on

A

Cellular Atypia

Epithelial Architectural Organisation

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13
Q

What are the categorisation of dysplasia

A

Low grade

High grade

Carcinoma in situ

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14
Q

What is meant by cytological changes

A

Changes in individuals cells reflecting abnormal DNA content in the nucleus, failure to mature and keratinise properly

e.g.
-Abnormal variation in nuclear size/shape
-Abnormal variation in cell size/shape

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15
Q

What is meant by architectural changes

A

These are changes in the organisation of maturation and normal layering of the epithelium

e.g.
-Irregular epithelial stratification
-Abnormal keratinisation

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16
Q

What would a low grade oral mucosa dysplasia be like

A

Easy to identify that the tumour originates from squamous epithelium

Architectural change into lower third

Cytological atypia or dysplasia may not be prominent

Shows a considerable amount of keratin production

Evidence of stratification

Well formed basal cell layer surrounding the tumour islands

Tumour islands are usually well defined and are often continuous with the surface epithelium

Invasion pattern with intact large branching rete pegs ‘pushing’ into underlying CT

17
Q

Where there is architectural change into middle third what descides if its low or high grade

A

level of cytological atypia

18
Q

What would a high grade oral mucosa dysplasia be like

A

Show little resemblance to a normal squamous epithelium

Architectural change upper third

Usually show considerable atypia
Invade in a non-cohesive pattern with fine cords, small islands and single cells infiltrating widely through the CT

Mitotic figures are prominent and many may be abnormal

19
Q

What would carcinoma in situ be like

A

Cytologically malignant but not invading

Abnormal architecture
-Full thickness (or almost full)
-Severe cytological atypia

Mitotic abnormalities frequent

20
Q

What are the histological prognostic factors

A

pattern of invasion

depth of invasion

Perinerural invasion

Invasion of vessels

21
Q

What is the oral cancer prognosis

A

1/3 patients present at stage I/II

-Stage I - 80% cure rate
-Stage II – 65% cure rate
-Later than this 5 year survival <50%, cure <30%
-If untreated, with metastases, survival is about 4 months