Skin Cancer Overview and Epidemiology Flashcards

1
Q

Types of skin cancer?

A

Malignant melanoma (most serious form of skin cancer)

Non-melanoma skin cancer:
Basal cell carcinoma (BCC)
Squamous cell carcinoma (SCC)

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2
Q

How do non-melanoma skin cancers arise?

A

From keratinocytes within the epidermis:

BCC arises from keratinocytes within the basal layer of the epidermis

SCC arise from supra-basal layers

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3
Q

How do malignant melanomas arise?

A

Arise from the melanocytes (pigment-forming cells) which are found scattered along the basal layer of the epidermis

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4
Q

Why is the incidence of skin cancer increasing?

A

Demographic and behavioural factors:

Ageing populations

UV exposure incidence increasing, inc. younger people

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5
Q

What % of skin cancers are malignant melanomas?

A

Only 5% of all skin cancers but 75% of deaths

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6
Q

What does melanoma survival depend upon?

A

Tumour depth:

Breslow thickness 4 mm confers a 50% melanoma survival

Metastases confers a 5% melanoma survival

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7
Q

Identification of a malignant melanoma?

A
A - asymmetry
B - border
C - colour
D - diameter
E - evolution
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8
Q

What is the “ugly duckling” sign?

A

Observation that naevi in the same individual tend to resemble one another, and that MM often deviates from this naevus pattern

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9
Q

Dermascopy of a malignant melanoma reveals?

A

Blue-white veil -irregular structureless area of confluent blue pigment with a ground glass haze, as if the image were out of focus
It is due to hyperkeratinisation over dense epidermal pigment

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10
Q

How common are BCCs?

A

Very common; comprise 75% of all non-melanoma skin cancers

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11
Q

Clinical presentation of BCC?

A

Slow-growing lump or non-healing ulcer; this is due to tumour : blood supply mismatch leading to cell death and central ulceration

PAINLESS and thus easily ignored

“Pearly” or translucent with visible, arborising blood vessels

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12
Q

Different names and types of BCC?

A

With a central ulceration - “rodent” ulcer

Scaly plaque - “superficial”

Infiltrative - “morphoeic”

Slightly scaly, irregular plaque with a thin, translucent rolled border and multiple microerosions - superficial

With dark/black coloured patches - pigmented BCC

Nodulocystic BCC presents as a solitary, shiny, red nodule with large telangiectatic vessels, often seen on the face - nodulocystic BCC

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13
Q

Spread of BCC?

A

LOCALLY INVASIVE. but rarely metastasise

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14
Q

Clinical presentation of SCC?

A

Presents in a no. of ways, e.g:
Hyperkeratotis (crusted) lumps lump/ulcer

May arise on sun-damaged skin and grow relatively FAST

May be painful and/or bleed

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15
Q

Differentiation of SCCs?

A

Majority are well-differentiated, low-risk SCC

Minority are poorly differentiated, high-risk SCC

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16
Q

Prognosis of SCC?

A

5% risk of metastases but, once this happens, the prognosis is poor

17
Q

Pre-cursor lesions of SCC?

A

Actinic keratoses - scaly spot found on sun-damaged skin; it is a pre-cursor or early form of cutaneous SCC; assoc. with a high risk of developing SCC or BCC

Bowen’s disease (carcinoma-in-situ) - AKA intra-epidermal carcinoma; an early stage of SCC

18
Q

What is keratoacanthoma?

A

Skin lesion that erupts in sun damaged skin; grows for a few months, then may shrink and resolve by itself

Considered to be a variant of the SCC

19
Q

What are cutaneous horns?

A

Hard conical projections from the skin, made of compact keratin; arise from benign, pre-malignant or malignant skin lesions

More common in elderly

20
Q

High risk sites for SCC?

A

Ears, lips, scalp

21
Q

Risk factors for skin cancer?

A

Sun exposure

Genetic predisposition

Immunosuppression

HPV infection

Transplant recipients

Other environmental carcinogens, e.g: coal tar, smoking, ionising radiation, arsenic, trauma, chronic ulceration (e.g: on the leg; they may become malignant)

22
Q

Genetic risk factors for skin cancers?

A

DNA repair syndromes, e.g: Xeroderma pigmentosum (defect in 1 of 7 nucleotide excision repair genes) causes photosensitivity, skin cancer on UV exposed sites, neurological deterioration and increased risk of other cancers

Albinism - no melanin/UV protection

Naevoid BCC (Gorlin’s syndrome) - autosomal dominant condition characterised by multiple and early onset BCCs, as well as other cancers

Dystrophic epidermolysis bullosa - autosomal recessive and increases the risk of SCC

Hereditary Type VII collagen deficiency (RDEB)

23
Q

Major features of Gorlin’s syndrome?

A

Multiple, early-onset BCCs

Palmar pits (on hands)

Jaw cysts

Ectopic calcification of the falx cerebri

24
Q

Minor features of Gorlin’s syndrome?

A

Skeletal abnormality

Macrocephaly, OFC > 97th centile (larger head circumference)

Cardiac/ovarian fibroma

Medullablastoma

25
Q

Prevention of skin cancer?

A
1. Behaviour:
Avoid sun at peak times
Utilise shade
Part. care of babies/children
Avoid sunbeds
  1. Clothing:
    Tightly woven, loose-fitting clothing (dark)
    Long sleeves, trousers, skirts
3. Sunscreens:
Broad spectrum (SPF25 +) with UVA protection
  1. Regular self-surveillance