9.2 Benign, premalignant and malignant tumours of relavence to dentistry Flashcards

1
Q

How have mouth cancer rates increased over the past decae?

A

Increase in cases by over 30%

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2
Q

Why do dentists play an important role in mouth cancer?

A
  • We see asymptomatic patients (check-ups) and are ideally placed to detect head and neck cancers at early stages
  • Dentists may be involved in the treatment of tumours in the head and neck, and treating patients with cancers at other sites
  • Restorative dentists may be involved in treating the dentition of mouth cancer pts
  • See patients over a period of years so can identify changes over time
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3
Q

What are the oral consequences of radio and chemo therapy?

A
  • Damage to salivary glands and salivary flow, xerostomia and increased caries risk
  • Risk of osteo-radionecrosis of the jaws
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4
Q

What is the most common oral malignancy?

A

Oral squamous cell carcinoma.

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5
Q

What is the difference between reactive vs neoplastic cell proliferations?

A

Reactive = response to a stimulus, lesion regresses when stimulus is removed

Neoplastic = proliferation of cells which is autonomous and persists after the initiating stimulus has been removed, can be benign or malignant.

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6
Q

What is the difference between hyperplasia and hypertrophy?

A

Hyperplasia = increase in number of cells
Hypertrophy = increase in size of cells

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7
Q

Name some reactive oral mucosal lesions.

A
  • Fibro-epithelial polyps
  • Fibrous epulis
  • Denture-induced granuloma
  • Pulp polyp
  • Pyogenic granuloma
  • Peripheral giant cell granuolma (giant cell epulis)
  • Traumatic ulcer
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8
Q

Name some neoplastic benign tumours of the oral cavity.

A
  • Squamous cell papilloma
  • Fibroma
  • Haemangioma
  • Lymphangioma
  • Neurofibroma
  • Neurilemmoma
  • Pleomorphic adenoma
  • Lipoma
  • Adenoma
  • Osteoma
  • Ossifying fibroma
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9
Q

Name some neoplastic malignant tumours of the oral cavity.

A
  • SCC
  • BCC (most common, rarely metastasise)
  • Malignant melanoma
  • Fibrosarcoma
  • Liposarcoma
  • Malignant lymphoma
  • Minor salivary gland adenocarcinomas
  • Osteosarcoma
  • Range of malignant salivary gland tumours
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10
Q

Which sites are most commonly affected by SCC?

A
  • Larynx, oral cavity and paranasal sinuses
  • Frequently metastasise to the lymph nodes of the neck with a poor long term survival rate
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11
Q

What is the 5 year survival rate for adults with mouth cancer in England?

A

56%

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12
Q

Where is mouth cancer most commonly located?

A
  • Tongue
  • Tonsils and oropharynx
  • Floor of mouth (under tongue)
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13
Q

What is the average size of oral cancer tumour at presentation?

A

3-4cm
Large! Late tumour, likely to have metastasised to lymph nodes of the neck.

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14
Q

What is the association between social class and mouth cancer?

A
  • Oral cancer 3 times more common in lowest social class vs highest
  • Poorer 5 year survival for those more deprived
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15
Q

Where is oral SCC usually found?

A
  • Lower lip (sun exposure)
  • Lateral margin of tongue
  • Ventral surface of tongue
  • Floor of mouth
  • Lingual sulcus
  • Retromolar area/fauces

75-80% of oral carcinomas occur at these sites.

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16
Q

Describe the possible appearance of oral SCC.

A
  • Ulcers (granular base)
  • Swellings
  • Red areas
  • Speckled leukoplakia
  • White areas
  • Firm areas (induration)
17
Q

What are the clinical features of advanced SCC?

A
  • Ulcer with raised, rolled edges
  • Exophytic, nodular mass
  • Reduced tongue mobility
  • Pain
  • Loose teeth
  • Mental anaesthesia/paraesthesia
  • Secondary deposits in lymph nodes
18
Q

What are some aetiological factors of mouth cancer?

A
  • Tobacco
  • Alcohol
  • UV light
  • Diet low in fruit and veg
  • Betel chewing
  • Infection
  • Irradiation
  • Immunosuppression
19
Q

Describe HPV related oropharyngeal cancer.

A
  • Affects the tonsils, base of tongue, soft palate
  • Affects younger age group than classic SCC
  • Associated with HPV-16 and HPV-18
  • More sensitive to chemotherapy
  • Better prognosis, up to 80% 5-year survival rate
20
Q

Describe the histopathology of oral SCC.

A
  • Arises from surface epithelium
  • Usually well differentiated and obviously squamous
  • Invades lamina propria and underlying tissues e.g. muscle, bone, salivary glands
21
Q

What term describes when cancer spreads to nerve tissue.

A

Perineural spread

22
Q

Describe the metastasis of oral SCC.

A
  • Cancer can invade lymphatics, nerves and blood vessels
  • Secondary deposits in submandibular and cervical lymph nodes are common
  • Blood borne metastases are rare but do occur
23
Q

Describe oral SCC treatment.

A
  • Surgical excision with a 5mm margin of normal tissue also removed
  • Reconstruction: free tissue transfer, pedicle flaps, prosthetic
  • Radiotherapy following surgical excision
  • Induction chemotherapy
  • Adjucant chem and radio therapy
24
Q

What is the long term prognosis for a patient with oral SCC?

A
  • Best prognosis is the lip (90%+)
  • Prognosis worsens as you go further back except for HPV related oropharyngeal cancer)
  • Poorly differentiated tumours have worse prognosis
  • Age of patient and comorbidities
  • Overall 50-60% 5-year survival
25
Q

Describe salivary gland tumours.

A
  • Relatively uncommon
  • Major glands = 80-85%
  • Minor glands = 15-20%
  • Parotid gland most common, followed by submandibular, sublingual rare
  • Minor glands: palate (55%), upper lip (20%), lower lip rare
26
Q

Are parotid gland tumours more commonly malignant or benign?

A
  • 85% benign
  • 15% malignant
27
Q

Which area is it common to find minor salivary gland tumours?

A

At the junction of the hard and soft palate.
About 45% of tumours at this site are malignant.

28
Q

Describe oral pre-cancerous lesions.

A
  • Cancer arising from pre-existing lesions of the oral mucosa
  • Leukoplakia and erythroplakia
  • Only a small number of pre-cancerous lesions become malignant (approx. 4% of leukoplakkia over 5-10 years)
  • Aetiological factors responsible for malignant transformation may be different from those producing the original lesion
29
Q

Describe erythroplakia as premalignant lesions.

A
  • Bright red velvety plaque that cannot be characterised clinically or pathologically as any other disease
  • High risk lesion, 50% become malignant over 10 years
  • Red patches are more worrying than white patches