Week 1- Oral carcinogenesis and dysplasia Flashcards

1
Q

What are characteristics of cancer?

A
  • Invasive tumour
  • Accumulation of mutations in DNA
  • Disruption in cell proliferation, differentiation and development
  • Abnormal, uncoordinated tissue growth
  • Local tissue invasion and destruction
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2
Q

What is the most common primary oral cancer tumour?

A

Squamous cell carcinoma (>90%)

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3
Q

How do we recognise oral cancer?

A
  • Oral Ulcerations (non-healing)
  • Red or white patches
  • Abnormal swellings
  • Loss of Tongue mobility
  • Cauliflower-like growths
  • Abnormal, localised tooth mobility
  • Non-healing tooth sockets
  • Colour changes in mucosa
  • Erosions in mucosa
  • Reduced/altered sensation
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4
Q

What is a type of secondary oral cancer tumour?

A

Metastatic adenocarcinomas

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5
Q

What % of patients with oral cancer will die in next 5 years?

A

50%

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6
Q

What are the next most common primary oral cancer tumours?

A
  • Minor salivary gland carcinomas
  • Lymphoma
  • Malignant melanoma
  • Sarcoma
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7
Q

What causes SSC?

A
  • Tobacco
  • Alcohol
  • Poor diet
  • Infections (HPV, candida)
  • Poor oral health
  • Low SES
  • Ageing
  • Immunosuppression
  • Genetic Predisposition
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8
Q

What does cannabis do to oral mucosa?

A

Increases permeability of oral mucosa. If you smoke and drink alcohol, you’re allowing those classic carcinogens to be more accessible to cells.

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9
Q

What are characteristics of normal oral mucosa?

A
  • Stratified squamous epithelium
  • Basal/spinous/granular/keratin
  • Rete ridges
  • Underlying dense CT lamina propria
  • Masticatory/specialised/lining
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10
Q

What are the 3 epidermal proliferative units?

A
  • Stem cells
  • Amplifying cells
  • Non-proliferative supra-basal cells
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11
Q

What happens if stem cell becomes over active?

A

They can become tumour initiating stem cells. (this process can be halted/reversed before progressing to cancer)

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12
Q

What happens when cells switch to malignancy?

A
  • Immortalisation and neurovascularisation
  • Cell migration
  • Local invasion and metastasis
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13
Q

What is oral epithelial dysplasia?

A

Histopathological term describing a spectrum of Tissue Dysmaturation & Disorganisation changes seen in biopsy specimens

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14
Q

What are cytology histopathological features of oral epithelial dysplasia?

A
  • Variation in Nuclear Size and Shape
  • Variation in Cell Size and Shape
  • Increased Nuclear to Cytoplasmic Ratio
  • Atypical Mitotic Figures
  • Increased Number & Size of Nucleoli
  • Hyperchromasia
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15
Q

What are tissue architecture histopathological features of oral epithelial dysplasia?

A
  • Irregular Epithelial Stratification
  • Loss of Polarity of Basal Cells
  • Drop-Shaped Rete Ridges
  • Increased Number of Mitotic Figures
  • Abnormally Superficial Mitoses
  • Premature Keratinisation in Single Cells (Dyskeratosis)
  • Keratin Pearls within Rete Ridges
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16
Q

What is the WHO grading system for oral epithelial dysplasia?

A
  • Mild
  • Moderate
  • Severe
  • Carcinoma-in-Situ
17
Q

What is the binary system for oral epithelial dysplasia?

A

Low Grade: lesions with <4 architectural or <5 cytological changes

High Grade

18
Q

What is the malignant transformation rate for mild/moderate dysplasia?

A

10.3%

19
Q

What are the malignant transformation rates for severe dysplasia/carcinoma in situ?

A

24.1%

20
Q

What is the overall malignant transformation rate?

A

12.3%