OC 11 - pathogenesis of HNC 3 Flashcards

1
Q

What is dysplasia?

A

a pre-malignant process

can be identified in many tissues

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2
Q

In tumour growth, what is the “initial event”?

A

initial event is where DNA damage occurs

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3
Q

In tumour growth, what is “mild dysplasia”?

A

damage has led to atypical proliferation of cells, but this is contained within the epithelium

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4
Q

In tumour growth, what is “severe dysplasia”?

A

full thickness of epithelium becomes involved - not invasive malignancy yet though because the tumour cells are still in the surface epithelium and havent breached the basement membrane

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5
Q

In tumour growth, what is “invasive malignancy”?

A

tumour cells have breached the basement membrane and are invading surrounding tissue

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6
Q

What is epithelial dysplasia?

A

a premalignant process - indicates a risk of developing carcinoma

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7
Q

In epithelial dysplasia, where are atypical epithelial alterations limited to?

A

limited to the surface squamous epithelium

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8
Q

What are architectural changes?

A

maturation and differentiation

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9
Q

What are cytological changes?

A

changes in cells

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10
Q

What is the key point to remember about epithelial dysplasia!

A

cells show abnormal features that are also seen in cancer cells but they do not yet possess the ability to invade adjacent normal tissues

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11
Q

What are the histological features of epithelial dysplasia?

A
  1. nuclear and cellular pleomorphism
  2. alteration in nuclear/cytoplasmic ratio (invariably an increase)
  3. nuclear hyperchromatism
  4. prominent nucleoli
  5. increased and abnormal mitoses
  6. loss of polarity of basal cells
  7. basal cell hyperplasia
  8. drop-shaped rete pegs
  9. irregular epithelial stratification or disturbed maturation
  10. abnormal keratinisation (dyskeratosis)
  11. loss/reduction of intercellular adhesion
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12
Q

What is nuclear and cellular pleomorphism?

A

variation in the size and shape of the nuclei and the cells themselves

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13
Q

What are ‘drop-shaped’ rete pegs?

A

wider at their deepest part

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14
Q

What is dyskeratosis?

A

cells start to keratinise before the surface is reached

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15
Q

What makes oral epithelial dysplasia different to oral SCC?

A

in dysplasia the atypical cells are confined to the surface, in SCC the atypical cells invade into the underlying connective tissue

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16
Q

What are the 3 categories in the WHO 2017 grading of epithelial dysplasia?

A

mild
moderate
severe (= carcinoma in situ)

17
Q

What are the WHO 2017 gradings of epithelia dysplasia based on?

A

based on 1/3 of epithelium

18
Q

What are the characteristics of mild dysplasia?

A

disorganisation, increased proliferation and atypia of basal cells

basal 1/3 of epithelium

19
Q

What are the characteristics of moderate dysplasia?

A

more layers of disorganised basaloid cells, atypia, suprabasal mitoses

extending to 2/3rds of the epithelium (basal and middle third)

20
Q

What are the characteristics of severe dysplasia?

A

very abnormal, affects full thickness of epithelium (all 3rds)

21
Q

What are oral potentially malignant disorders?

A

oral mucosal lesions that have a potential risk of developing into oral SCC

22
Q

What are some oral potentially malignant disorders?

A
  • Leukoplakia
  • Erythroplakia
  • Erythroleukoplakia
  • Oral submucous fibrosis
  • Syphilitic glossitis
  • Dyskeratosis congenita
  • Chronic candidiasis
  • Lichen planus
  • Discoid lupus erythematosus
  • Smokeless tobacco keratosis
  • Palatal lesions associated with reverse smoking
  • Actinic keratosis (lip only)
23
Q

What is oral submucous fibrosis?

A

pale fibrous bands
- progressive deposition of collagen in the submucosal tissue, also associated with atrophy of the surface epithelium