15 - Dysplasia and oral cancer 2 Flashcards

1
Q

Define a potentially malignant lesion.

A
  • a lesion that is becoming cancer
  • more likely to become cancer
  • only potentially malignant
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2
Q

What lesions are commonly referred to as potentially malignant lesions?

A
  • leukoplakia
  • erythroplakia
  • lichen planus
  • candidal leukoplakia
  • chronic hyperplastic candidiasis
  • oral submucous fibrosis
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3
Q

What is the estimated malignant change for leukoplakia?

A

2.5% in 10 years

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4
Q

Where do most oral carcinomas arise in the UK population?

A

Clinically normal mucosa

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5
Q

What is the estimated malignant change for erythroplakia?

A

50% maybe already be carcinoma

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6
Q

What are the categories of dysplasia?

A
  • low grade
  • high grade
  • carcinoma-in-situ
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7
Q

What are the categories of dysplasia based on?

A
  • cellular atypia
  • epithelial architectural organisation
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8
Q

What are the prognostic factors in histology?

A
  • pattern of invasion
  • depth of invasion
  • perineural invasion
  • invasion of vessels
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9
Q

How does the pattern of invasion impact diagnosis?

A

Bulbous rete pegs infiltrating at same level have a better prognosis than widely infiltrating small islands and single cells

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10
Q

How does the depth of invasion impact diagnosis?

A

Risk of metastases for tumours bigger than 4mm is 4x greater than those smaller than 4mm

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11
Q

How does the perineural invasion impact diagnosis?

A
  • seen in 60% of OSCC
  • most significant when tumour is within large nerve at a site far from the main tumour mass
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12
Q

How does the invasion of vessels impact diagnosis?

A

Associated with lymph nodes metastases and poor prognosis

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13
Q

What are the stages of dysplastic tissue?

A
  • normal keratinocytes
  • genetic instability or aneuploidy
  • adaptive changes
  • invasion (cancer)
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14
Q

Define aneuploidy.

A

Abnormal amount of chromosomes in a haploid cell (only one set of chromosomes)

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15
Q

What is field cancerisation?

A
  • if one area is exposed to carcinogen then multiple primary cancers can be developing, some at different rates to others
  • high risk site within 5cm of original primary (whole mouth/pharynx)
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16
Q

Define a synchronous lesion.

A

Primary cancer that develops at the same time and similar rate to the original primary

17
Q

Define a metachronous lesion.

A

Primary cancer that develops after the original primary but is from the same field cancerisation

18
Q

What are the stages of oral cancer?

A

T - size
N - lymph nodes
M - metastases

19
Q

What is the cure rate for stage I oral cancer?

A

80%

20
Q

What is the cure rate for stage II oral cancer?

A

65%

21
Q

Describe lip cancer.

A
  • lower lip, non-helaign ulcer or swelling
  • causes include sunlight and smoking
  • slow growth with local invasion, rarely metastasises
  • good prognosis due to early detection
22
Q

What are the different oral cancer screening tools?

A
  • HPV16 screening
  • toluidene blue
  • VELscope
  • photodynamic diagnosis (PDD)
  • clinical judgement of experienced clinician
23
Q

How does toluidene blue act as a screening tool?

A
  • dyes tissues blue
  • 50% false negatives as also dyes inflammatory lesions
  • can be used for selection of biopsy site
24
Q

How does VELscope act as a screening tool?

A
  • autofluorescence of tissue with blue light
  • loss of fluorescence indicates change but not cause
25
Q

What is involved in primary prevention of oral cancer?

A
  • smoking cessation advice
  • alcohol reduction advice
  • diet advice
  • regular STE
  • monitor any suspicious lesions and refer when threshold met