Benign skin conditions Flashcards

1
Q

Features of seborrhoeic keratoses

A
  • large variation in colour from flesh to light-brown to black
  • have a ‘stuck-on’ appearance
  • keratotic plugs may be seen on the surface
  • very common, related to skin aging
  • an occur anywhere other than palms and soles and mucous membranes
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2
Q

Management of seborrhoeic keratoses

A
  • reassurance about the benign nature of the lesion is an option
  • options for removal include curettage, cryosurgery and shave biopsy
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3
Q

Spot diagnosis

A

seborrhoeic keratosis

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4
Q

Spot diagnosis

A

Seborrhoeic keratosis

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5
Q

Spot diagnosis

A

Seborrhoeic keratoses

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6
Q

Another name for cherry hemangiomas

A

Cherry haemangiomas (Campbell de Morgan spots)

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7
Q

What are cherry haemangiomas?

A

Cherry haemangiomas (Campbell de Morgan spots)

  • benign skin lesions which contain an abnormal proliferation of capillaries
  • unknown cause
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8
Q

Features of cherry haemangiomas

A

aka Campell De Morgan spots

  • They are more common with advancing age and affect men and women equally
  • May develop on any part of the body but they appear most often around the mid trunk
  • Increase in number from about the age of 40
  • erythematous, papular lesions
  • typically 1-3 mm in size
  • non-blanching
  • not found on the mucous membranes
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9
Q

Management of Cherry Haemangiomas

A

As they are benign no treatment is usually required

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10
Q

Spot diagnosis

A

Cherry haemangioma (Campbell De Morgan)

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11
Q

Spot diagnosis

A

Pyogenic granuloma

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12
Q

What’s Pyogenic Granuloma

A

Pyogenic granuloma

  • a relatively common benign skin lesion
  • name is confusing as they are neither true granulomas nor pyogenic in nature
  • multiple alternative names e.g. ‘eruptive haemangioma’
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13
Q

Features of pyogenic granuloma

A
  • most common sites are head/neck, upper trunk and hands
  • Lesions in the oral mucosa are common in pregnancy
  • initially small red/brown spot → rapidly progress within days to weeks forming raised, red/brown lesions which are often spherical in shape
  • the lesions may bleed profusely or ulcerate
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14
Q

Management of pyogenic granuloma

A
  • lesions associated with pregnancy often resolve spontaneously post-partum
  • other lesions usually persist
  • Removal methods include curettage and cauterisation, cryotherapy, excision
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15
Q

Spot diagnosis

A

Pyogenic granuloma

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16
Q

What’s dermatofibroma?

A
  • Solitary dermal nodules
  • Usually affect extremities of young adults
  • Lesions feel larger than they appear visually
  • Histologically they consist of proliferating fibroblasts merging with sparsely cellular dermal tissues

-No treatment required if diagnosis is confident

17
Q

Dermatofibroma O/E

A
  • Site of minor trauma – insect bite
  • Brownish/red dermal lesion
  • Feels firm
  • Pinching the tumour between fingers leads to dimpling / sinking down into the dermis
18
Q

Dimple / buttonhole / pinch sign = ?

A

Dimple / buttonhole / pinch sign = dermatofibroma

19
Q

What’s Congenital Melanocytic Naevi

A
  • Typically appear at, or soon after, birth
  • Usually greater than 1cm diameter
  • Increased risk of malignant transformation (increased risk greatest for large lesions)
20
Q

What’s atypical naevus syndrome?

A
  • Atypical melanocytic naevi that may be autosomally dominantly inherited
  • Some individuals are at increased risk of melanoma (usually have mutations of CDKN2A gene
  • Many people with atypical naevus syndrome AND a parent sibling with melanoma will develop melanoma
21
Q

Actinic keratosis O/E

A
  • Flaky / keratotic patches
  • Bald scalps, foreheads, ears, dorsum of hands and forearms
  • Feel crusty
22
Q

What’s an epidermoid cyst?

A
  • Common and affect face and trunk
  • They have a central punctum, they may contain small quantities of sebum
  • The cyst lining is either normal epidermis (epidermoid cyst) or outer root sheath of hair follicle (pilar cyst)
23
Q

What’s actinic keratoses?

A

Actinic, or solar, keratoses (AK)

  • a common premalignant skin lesion
  • develops as a consequence of chronic sun exposure
24
Q

Features of actinic keratoses

A
  • small, crusty or scaly, lesions
  • may be pink, red, brown or the same colour as the skin
  • typically on sun-exposed areas e.g. temples of head
  • multiple lesions may be present
25
Q

Management of actinic keratoses

A
  • prevention of further risk: e.g. sun avoidance, sun cream
  • fluorouracil cream: typically a 2 to 3 week course. The skin will become red and inflamed - sometimes topical hydrocortisone is given following fluorouracil to help settle the inflammation
  • topical diclofenac: may be used for mild AKs. Moderate efficacy but much fewer side-effects
  • topical imiquimod: trials have shown good efficacy
  • cryotherapy
  • curettage and cautery
26
Q

What’s Bowen’s disease?

A

Bowen’s disease

  • a type of intraepidermal squamous cell carcinoma
  • more common in elderly females
  • around a 3% chance of developing invasive skin cancer
27
Q

Features of Bowen’s disease

A
  • red, scaly patches
  • often occur on sun-exposed areas such as the lower limbs
  • Well defined scaly plaque
  • No raised edge
28
Q

Management of Bowen’s disease

A
  • topical 5-fluorouracil or imiquimod
  • cryotherapy
  • excision
29
Q

Advice on sun protection

A
  • How to recognise sunburn
  • Avoid the strong sun – (11am – 3pm)
  • Cover up – hats, t-shirts, sun glasses
  • Use Factor 50
  • Know your skin type
  • UV index
  • Avoid sunbeds
  • Vitamin D
30
Q

Skin types

A

Skin type is an important risk factor for skin cancer. Skin types may be classified according to Fitzpatrick classification:

  • I: Never tans, always burns (often red hair, freckles, and blue eyes)
  • II: Usually tans, always burns
  • III: Always tans, sometimes burns (usually dark hair and brown eyes)
  • IV: Always tans, rarely burns (olive skin)
  • V: Sunburn and tanning after extreme UV exposure (brown skin, e.g. Indian)
  • VI: Black skin (e.g. Afro-Caribbean), never tans, never burns