Squamous Cell Carcinoma Flashcards

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1
Q

What is squamous cell carcinoma?

A

SCC = 2nd most common skin cancer

SCC is derived from keratinocytes like BCC

Higher metastatic potential then BCC
=> invasive disease
=> sometimes metastasise & can be fatal

May arise from solar keratoses or Bowen’s disease

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2
Q

Who is at risk of SCC?

A

Risk factors for SCC:

=> More common in elderly male patients

=> Previous SCC or another form of skin cancer

=> Actinic keratoses

=> Outdoor occupation or recreation

=> Smoking

=> Fair skin, blue eyes and blond or red hair

=> Previous cutaneous injury, thermal burn, disease (eg cutaneous lupus, epidermolysis bullosa, leg ulcer)

=> Inherited syndromes: SCC high risk in xeroderma pigmentosum and albinism

=> Organ transplant recipients have a massively increased risk of developing SCC.

Other risk factors include:

=> ionising radiation

=> exposure to arsenic

=> immune suppression due to disease (eg chronic lymphocytic leukaemia) or medicines

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3
Q

What causes SCC?

A

> 90% of SCC associated with DNA mutations

=> Mutations in p53 tumour suppressor gene caused by exposure to UVB

=> Other mutations related to cigarette smoking, ageing and immune suppression i.e.azathioprine

=> Mutations in signalling pathways affect the epidermal growth factor receptor, RAS, Fyn, and p16INK4a signalling.

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4
Q

What are the clinical features of SCC?

A

Enlarging scaly or crusted lumps

Usually arise within pre-existing actinic keratosis or intraepidermal carcinoma

Grow over weeks to months

May ulcerate

Tender / painful

Located on sun-exposed sites i.e. face, lips, ears, hands, forearms and lower legs

Size varies from a few millimetres to several centimetres in diameter

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5
Q

What are the types of SCC?

A

Distinct clinical types of invasive cutaneous SCC include:

=> Cutaneous horn - the horn is due to excessive production of keratin

=> Keratoacanthoma - a rapidly growing keratinising nodule that may resolve without treatment

=> Carcinoma cuniculatum (verrucous carcinoma) - slow-growing, warty tumour on the sole of the foot.

The pathologist may classify a tumour as well differentiated, moderately well differentiated, poorly differentiated or anaplastic cutaneous SCC.

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6
Q

How is SCC classified?

A

SCC is classified as low-risk or high-risk depending on the chance of tumour recurrence and metastasis.

Characteristics of high-risk SCC include:

=> Diameter >2cm

=> Location on the ear, vermilion of the lip, central face, hands, feet, genitalia

=> In elderly or immune suppressed patient

=> Histological thickness >2mm, poorly differentiated histology, or with the invasion of the subcutaneous tissue, nerves and blood vessels

=> Metastatic SCC found in regional lymph nodes (80%), lungs, liver, brain, bones and skin

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7
Q

How is SCC staged?

A

Tumour staging for SCC:
T0: No evidence of a primary tumour

Tis: Carcinoma in situ

T1: Tumour ≤ 2cm without high-risk features

T2: Tumour ≥ 2cm; or; Tumour ≤ 2 cm with high-risk features

T3: Tumour with the invasion of maxilla, mandible, orbit or temporal bone

T4: Tumour with the invasion of axial or appendicular skeleton or perineural invasion of skull base

Nodal staging for cutaneous SCC:
N0: No regional lymph node metastasis

N1: Metastasis in one local lymph node ≤3cm

N2: Metastasis in one local lymph node ≥3cm; or; Metastasis in >1 local lymph node ≤6cm

N3: Metastasis in lymph node ≥6cm

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8
Q

How is SCC diagnosed?

A

Clinical diagnosis

Diagnosis + histological subtype confirmed pathologically by diagnostic biopsy or after excision

Patients with high-risk SCC undergo staging investigations to determine spread of disease:

=> Imaging using ultrasound scan, X-rays, CT scans, MRI scans

=> Lymph node or other tissue biopsies

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9
Q

How is SCC treated?

A

Surgical treatment

=> Excised with a 3–10 mm margin of normal tissue around a visible tumour.
=> A flap or skin graft needed to repair the defect

Other methods of removal include:

=> Shave, curettage, and electrocautery for low-risk tumours on trunk and limbs

=> Aggressive cryotherapy for very small, thin, low-risk tumours

=> Mohs micrographic surgery for large facial lesions with indistinct margins or recurrent tumours

=> Radiotherapy for inoperable tumour, patients unsuitable for surgery, or as adjuvant

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10
Q

How is advanced or metastatic SCC treated?

A

Locally advanced primary, recurrent or metastatic SCC => multidisciplinary consultation with a combination of treatments

=> Surgery

=> Radiotherapy

=> Cemiplimab

=> Experimental targeted therapy using epidermal growth factor receptor inhibitors

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11
Q

How can SCC be prevented?

A

=> Careful sun protection - important in ageing, sun-damaged, fair skin, immune-suppressed and those with actinic keratoses or previous SCC

=> Stay indoors or under the shade in the middle of the day

=> Wear covering clothing

=> Apply high protection factor SPF50+ broad-spectrum sunscreens

=> Avoid indoor tanning i.e. sunbeds

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12
Q

What is the prognosis of SCC?

A

Most SCCs are cured by treatment.

=> cure most likely small lesion treated

=> ~50% of people at high risk of SCC develop a second one within 5 years of the first

=> They are also at increased risk of other skin cancers, especially melanoma

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