Skin Cancers Flashcards

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1
Q

What is BCC?

A
  • A slow growing, locally invasive malignant tumour of the epidermal keratinocytes
  • Normally in older individuals
  • Rarely metastasises
  • Most common malignant skin tumour
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2
Q

What are the risk factors for BCC?

A
  • Excessive sun exposure
  • Hx of frequent sunburn in childhood
  • Type 1 skin type (fair skin, red hair, blue eyes)
  • Increasing age
  • Male sex
  • Immunosuppression
  • Prev. Hx. of skin cancer
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3
Q

What is the clinical presentation of BCC?

A
  • Nodular (= most common type)
  • Slow growing
  • Small, skin-coloured papule or nodule
  • Pearly-rolled edge
  • Telangiectasia
  • Central ulceration
  • Arborising vessels on Dermoscopy
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4
Q

What is the management of BCC?

A
  • Surgical excision (= gold standard)
  • Curettage
  • Topical treatment (if superficial + low-risk)
  • > Imiquimod
  • Moh’s Micrographic Surgery (for high-risk, recurrent tumours)
  • Chemo
  • > Vismodegib
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5
Q

What is Vismodegib used for?

A
  • Chemo
  • for locally-advanced BCC not suitable for surgery or radiotherapy
  • Metastatic BCC
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6
Q

What is SCC?

A
  • Locally invasive malignant tumour of the epidermal keratinocytes
  • Potential to metastasise
  • In-situ = Bowen’s disease
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7
Q

What are the risk factors for SCC?

A
  • Excessive UV (sun) exposure
  • HPV (genital SCC)
  • Smoking (lip SCC)
  • Outdoor occupation
  • Caucasian ethnicity
  • Increasing age
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8
Q

What is the Clinical Presentation of SCC?

A
  • Usually on sun-exposed sites
  • Faster growing (than BCC)
  • Tender
  • Scaly/crusted (keratotic)
  • Fleshy growths
  • Can ulcerate
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9
Q

What is the Management of SCC?

A
  • Surgical excision
  • +/- RT (large + non-resectable nodes)
  • Follow-up if high-risk
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10
Q

What are the risk factors for high-risk SCC lesions?

A
  • Immunosuppressed
  • > 20mm diameter
  • > 4mm depth
  • Ear, nose, lip, eyelid
  • Perineural invasion
  • Poorly differentiated -> tends to metastasise!
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11
Q

What is Keratocanthoma?

A
  • Varient of SCC
  • Erupts from hair follicles in sun damaged skin
  • Grows rapidly -> may shrink after a few months and resolve
  • Surgical excision (tends to resolve itself by the time surgery-time comes)
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12
Q

What is Malignant Melanoma?

A
  • Malignant tumour of the Epidermal Melanocytes

- Potential to Metastasise

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13
Q

What are the risk factors for Malignant Melanoma?

A
  • Excessive UV (sun) exposure
  • Type 1 skin type (fair skin, red hair, blue eyes)
  • Hx. of multiple or atypical moles
  • PMH or FH of Melanoma
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14
Q

How can you identify between a normal mole and melanoma?

A
  • “ABCDE” symptoms*
  • Asymmetrical – melanomas usually have 2 very different halves and are an irregular shape
  • Border – melanomas usually have a notched or ragged border
  • Colours – melanomas will usually be a mix of 2 or more colours
  • Diameter – most melanomas are usually >6mm in diameter
  • Evolution: enlargement or elevation – a mole that changes size over time is more likely to be a melanoma
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15
Q

Which instrument would you use to identify a suspicious mole?

A
  • Dermatoscope
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16
Q

What are the different types of Melanoma?

A
  • Superficial Spreading Malignant Melanoma
  • Lentigo Maligna Melanoma
  • Nodular Melanoma
  • Acral Lentiginous Melanoma/Subungal Melanoma
  • Ocular Melanoma
17
Q

What is the management of Malignant Melanoma?

A
  • Depends on stage and Breslow thickness*
  • Surgical excision (= definitive treatment)

Metastasis or adjuvant therapy:

  • Immunotherapy
  • Chemo
  • Regular follow-up
  • Primary and secondary prevention
18
Q

What is Breslow Thickness?

A
  • Measures the depth of the Melanoma from the surface of the skin, down to the deepest part of the tumour
  • Helps determine the stage of the cance
  • > guides treatment and determines prognosis
19
Q

What is the general prognosis of Malignant Melanoma?

A

90% of people diagnosed with Melanoma in England and Wales survived 10 years or more

20
Q

What are the 2 most common Cutaneous Lymphomas?

A
  • Mycosis Fungoides
  • Sezary syndrome

(both are sub-types of Cutaneous T Cell lymphoma → CTCLs make up 65% of all Cutaneous Lymphomas)

21
Q

What is the most common CTCL?

A

Mycosis Fungoides

22
Q

What are the identifying features of Mycosis Fungoides?

A
  • Patch (difficult to differentiate from eczema/psoriasis) -> Plaques -> Tumour (large, irregular, can ulcerate) -> Metastases (LNs, blood, solid organs)
  • Work up includes bloods for sezary cells, and CT imaging for staging
23
Q

What are the identifying features of Sezary syndrome?

A
  • “Red Man syndrome” -> >80% BSA
  • CTCL affecting the entire body:
  • > skin thickened, scaly and red
  • > vv itchy
  • LN involvement
  • Sezary cells in peripheral blood
  • > atypical T cells
  • Poor prognosis
  • > median survival 2-4yrs
  • > opportunistic infection
  • Treatment = Extracorporeal Photophoresis