DERM Revision 2 Flashcards

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1
Q
A
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2
Q

Describe the pathophysiology of acne vulgaris [3]

A

Increase in Sebum Production:
- Primarily driven by hormonal (particularly testosterone) changes - stimulate sebaceous glands to produce more sebum

Follicular Hyperkeratinisation:
- abnormal keratinocyte proliferation and differentiation within the pilosebaceous unit
- results in the formation of a keratinous plug known as a microcomedo

Colonisation with P. acnes:
- The lipid-rich environment created by increased sebum production also promotes overgrowth of anaerobic bacteria like P. acnes

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3
Q

How do you differentiate acne to rosacea? [2]

A

Acne have comedones
- open (blackheads)
- closed (whiteheads)
- Scarring common

Rosacea:
- Rosacea often includes symptoms of flushing and ocular involvement which are not seen in acne vulgaris.
- The absence of scarring is more typical for rosacea

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4
Q

Describe what is meant by acne fulminans [1]

A

Acne fulminans
- severe form of acne conglobata with systemic features such a fever, arthralgia and lymphadenopathy.
- Hospital admission is often required and the condition usually responds to oral steroids

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5
Q

Describe how you treat mild [3], moderate [3] or severe acne [1]

A

NB can also use: antiandrogens e.g. spironolactone, cyproterone acetate

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6
Q

What is important to note about using abx to treat acne vulgaris? [1]

A

Topical AND oral antibiotics should not be used in combination in the treatment of acne

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7
Q

Alternative to repeated courses of isotretinoin = ? [2]

A

oral contraceptives e.g. microgynon

antiandrogens e.g. spironolactone, cyproterone acetate

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8
Q

Describe the clinical manifestatio of acne vulgaris [3]

A

Comedone Formation
- Closed comedones (whiteheads) occur when the follicular opening is obstructed completely
- Open comedones (blackheads) form when there is partial obstruction with exposure to air causing oxidation of melanin or lipids within the sebum.

Papule and Pustule Development
- inflammation persists around a blocked follicle, it can evolve into papules—small raised bumps indicating underlying inflammation without pus formation.

Nodule and Cyst Formation

Scarring can occur

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9
Q

Folliculitis is an inflammation of the hair follicles caused by bacterial infection, most commonly Staphylococcus aureus. It can mimic acne vulgaris but there are several distinguishing characteristics.

What are they? [3]

A
  • Folliculitis lesions tend to have a more uniform appearance
  • Distribution of folliculitis can occur anywhere there is hair growth (face, chest and back as with acne vulgaris)
  • The presence of pruritus (itching) is more common in folliculitis than in acne vulgaris.
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10
Q

Perioral dermatitis presents as small papules and pustules around the mouth area. This condition can be mistaken for acne vulgaris due to similar lesion types; however, it differs which ways?

A

Limited to the perioral area (around the mouth), periocular area (around the eyes) or nasolabial folds, whereas acne vulgaris commonly affects the face, chest and back.

No comedones

Perioral dermatitis may appear scaly or dry, unlike acne vulgaris.

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11
Q

Describe the mangement of mild, moderate and severe acne vulgaris [+]

A

Mild: 12 week topical combination of any of the following:
* a fixed combination of topical adapalene with topical benzoyl peroxide
* a fixed combination of topical tretinoin with topical clindamycin
* a fixed combination of topical benzoyl peroxide with topical clindamycin

Moderate to severe acne: a 12-week course of one of the following options:
* a fixed combination of topical adapalene with topical benzoyl peroxide
* a fixed combination of topical tretinoin with topical clindamycin
* a fixed combination of topical adapalene with topical benzoyl peroxide + either oral lymecycline or oral doxycycline
* a topical azelaic acid + either oral lymecycline or oral doxycycline

Severe - not responding to treament
- Oral isotretinoin (derived from vitamin A and is a powerful anti-inflammatory agent)

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12
Q

NICE guideline 198 (June 2021) advises considering oral isotretinoin use in those over the age of 12 who have failed treatment with topical therapies and systemic antibiotics.

Examples include [4]

A

Nodulocystic acne
Acne conglobata
Acne fulminans
Acne at risk of permanent scarring

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13
Q

Name a side effect of using tetracylines for acne treatment if used in children under 8 years of age or in pregnant women? [1]

A

permanent teeth discolouration

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14
Q

What risks occur with isotretinoin prescription? [5]

A

Teratogenicity
hyperlipidaemia
hepatotoxicity
Sexual side effects: erectile disfunction, loss of libido, vaginal dryness
Photosensitivity
Depression & ? suicide ideation

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15
Q

What monitoring should you perform when prescribing isotretinoin? [3]

A

Liver function tests
Lipids
Pregnancy tests in female patients

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16
Q

Name this type of melanoma [1]
What sign is shown here? [1]

A

Subungual melanoma

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17
Q

Name this type of melanoma [1]

Characteristics? [+]

A

Amelanotic Melanoma
- no melanin
- firm
- grow fast
- look harmless

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18
Q

What does the Breslow thickness (mm) of a MM mean? [1]

What does the Clark level (I-V) refer to? [1]

What thickness inidcates a thin [1] and thick melanoma [1]

A

Breslow thickness (BT) is based on the vertical thickness of the tumour in millimetres.

Clark level (I-V) is a histological classification with estimated prognosis based upon the anatomical level of invasion into the skin.

Breslow Thickness and Clark level
Thin melanoma: < 0.8mm
Thick melanoma: >0.8mm

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19
Q

Describe the characteristics of Basal Cell Carcinoma (BCC)

A
  • Shiny pink/red lump
  • Slow growing, over months to years
  • Sometimes red flat patches
  • Form a recurrent crust that doesn’t heal
  • Over time bleed/ulcerate in the middle, but may not be painful
  • Usually sun-exposed sites: face, ears, scalp, hands, upper trunk
  • Rarely metastasise

TURP: Telangiectasia Ulceration Rolled edges Pearly edges

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20
Q

Which type of skin cancer is most common? [1]

A

Basal Cell Carcinoma (BCC) (75%)

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21
Q

Which genetic conditions are a risk factor for BCC? [2]

A

Genetic disease:
* Gorlin syndrome
* Xeroderma pigmentosum

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22
Q

Describe test often perform in clinic to test for BCC [1]

A
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23
Q

Describe this type of BCC [1]

A

Morphoeic BCC
- sclerotic (scarred)

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24
Q

Describe the Dx [2] and Mx [3] of BCC

A

Diagnosis
History
Skin biopsy from ulcer edge

Management
Excision
Radiotherapy
Superficial BCCs – 5-flourouracil or imiquimod cream

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25
Q

Describe the characteristics of SCC [+]

A
  • Enlarging scaly/crusted lumps
  • Grow rapidly over weeks
  • May ulcerate
  • Often tender/painful/bleed (except in IC ptx)
  • Usually arise within pre-existing actinic keratosis or intraepidermal carcinoma
  • Commonly face, lips, ears, hands and limps
  • Rarely metastasises
  • Often have hyperkerotic horn / no rolled border
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26
Q

Dx? [1]
Describe this [1]

A

Actinic Keratoses
- hyperkeratotic papules on a background of sun-damaged skin
- Actinic keratosis involves the formation of precancerous scaly lesions on the skin
- Actinic keratoses have around a 10% risk of developing into an SCC, therefore monitoring and treatment are important

27
Q

Superficial form of SSC = ? [1]

A

Bowens Disease

28
Q

H

Describe the characteristics of Seborrheic Keratoses [+]

A
  • Very common
  • Present in >90% of people over 60
  • Increase in number with time
  • Often develop in middle aged
  • Waxy or warty surface
  • Flat or plaques
  • Stuck on appearance
29
Q

Name and describe this type of skin condition [3]

A

Junctional Naevi
* Mole
* Flat
* Pigmented
* Regular, symmetrical, static appearance

GO over

30
Q

What are solar lentigo?

A

Solar lentigo
- is a harmless patch of darkened skin. It results from exposure to ultraviolet (UV) radiation, which causes local proliferation of melanocytes and accumulation of melanin within the skin cells (keratinocytes)
- aka sun spots

31
Q

Name and describe this type of skin condition [3]

A
  • Compound Naevi
    Mole
    Central raised area
    Surrounded by flat pigmentation
32
Q

On palm of hands or feet

Dx? [1]

A

Acral Naevi

33
Q

Name and describe this type of skin condition [1]

A

Naevus Spilus
- Nevus spilus, also known as speckled lentiginous nevus, is a light brown or tan birth mark, speckled with small, dark spots or small bumps.
- Malignant change very rare

34
Q

https://www.passmedicine.com/menu.php#

A
35
Q

What are risk factors for malignant melanoma? [5]

A

UV Radiation
- UVB causes direct DNA damage

Skin Type
- (Fitzpatrick Skin types I & II)

Melanocytic naevi
- multiple (>100) or giant (>20 cm) naevi
- Congenital melanocytic naevi (moles present from birth, or that develop within the first few months after birth, are called congenital melanocytic nevi)
- Atypical mole syndrome (AMS): >1 pigmented lesions on the iris; >1 naevi on buttocks or instep naevi on anterior scalp; ≥2 atypical naevi; >100 naevi

Genetics
- CDK4, xeroderma pigmentosum, melanocortin 1 receptor

Previous skin cancer
- Previous melanoma

Immunosuppression
- HIV/AIDS
- Organ transplant recipient
- Lymphoproliferative disease
- Anti-TNF treatment

36
Q

Which is the most common place to get MM in men?

Skin of lower limb
Skin of trunk
Skin of upper limb
Head or neck

A

Which is the most common place to get MM in men?

Skin of lower limb
Skin of trunk
Skin of upper limb
Head or neck

37
Q

Which is the most common place to get MM in women?

Skin of lower limb
Skin of trunk
Skin of upper limb
Head or neck

A

Which is the most common place to get MM in women?

Skin of lower limb
Skin of trunk
Skin of upper limb
Head or neck

38
Q

Histologically, melanomas are divided into five major subtypes.

What are they? [5]

A

Superficial spreading (70%)
Nodular (15%)
Lentigo maligna (10%)
Acral lentiginous (< 5%)
Desmoplastic melanoma (< 1%)

39
Q

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

40
Q

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

41
Q

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Lentigo maligna
- Lentigo maligna is an early form of melanoma in which the malignant cells are confined to the tissue of origin, the epidermis
, hence it is often reported as ‘in situ’ melanoma. It occurs in sun damaged skin so is generally found on the face or neck, particularly the nose and cheek. It grows slowly in diameter over 5 to 20 years or longer.

42
Q

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

43
Q

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

44
Q

Which of the following are typically more seen at a more advanced stage.

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

Which of the following are typically more seen at a more advanced stage.

They transition immediately into the vertical growth phase. Because of this, it is usually diagnosed at a more advanced stage.

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

45
Q

[] occurs in the elderly on chronically sun-exposed sites.

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

A

[] occurs in the elderly on chronically sun-exposed sites.

Superficial spreading
Nodular
Lentigo maligna
Acral lentiginous
Desmoplastic melanoma

46
Q

How do you investigate for MM? [1]

A

All patients require a careful skin and lymph node examination.
- ALWAYS send for histology
- Suspicious lesions should be excised with a narrow (2mm) margin
- NEVER shave or curette a suspected melanoma

47
Q

Management is complex and guided by the Melanoma Multidisciplinary Team (MDT).

Describe the different treatment options

A

Surgical:
- WLE represents the standard treatment for primary melanoma. Involves removal of the biopsy scar with a surrounding margin of ‘healthy’ skin, with fat, down to muscular fascia. This margin is determined by the Breslow thickness.
- Sentinel Lymph Node Biopsy (SLNB)
- Electrochemotherapy is a relatively new therapy for patients with locally advanced melanoma.

Medical (typically adjuvant therapy)
- Chemotherapy
- Radiotherapy
- Immunotherapy

48
Q

Which factors determine if a MM prognosis? [5]

A

Breslow thickness
Clark level
Ulceration - . It is suggestive of an aggressive tumour phenotype with greater likelihood for invasion and metastasis.
Mitotic index (an indicator of cell turnover) is also an important histological finding.

49
Q

Describe what is meant by Gorlin syndrome [1]

A

A rare autosomal dominant condition that occurs as a result of gene mutation, specifically the PTCH1 gene. Individuals with Gorlin syndrome typically begin to develop BCCs during adolescence or early adulthood.

50
Q

What are the clinical sub-types of BCC? [5]

Describe how the present

A

There are several clinical sub-types of BCC, including:
nodular
- red / flesh-coloured and have well-defined borders with overlying telangiectasias. As they grow, they may develop central ulceration (Rodent ulcer).

superficial
- slow-growing erythematous plaques that may be dry or crusted or have a slight bluish tinge

morphoeic
- scar-like lesion or indentation; they commonly occur on the upper trunk or face.

pigmented
- Pigmented BCCs may be difficult to distinguish from melanoma.

basosquamous:
- A rare, but aggressive form of BCC with increased risk of recurrance and even metastasis.

51
Q

Types of BCC:

[] and [] BCCs are considered low-risk, whereas [] is high-risk due to their extensive local spread and high recurrence rate.

A

Nodular and superficial BCCs are considered low-risk, whereas morpheaform is high-risk due to their extensive local spread and high recurrence rate.

52
Q

Describe the different treatment options for low and high risk BCC [+]

A

The main goal of treatment is the complete removal of the tumour with preservation of the function and cosmesis of the affected area.

The type of treatment depends on whether the BCC is low or high risk

Low risk:
- complete surgical removal or electrodesiccation and curettage (ED&C)
- Superficial BCCs – 5-flourouracil or imiquimod cream

High risk
- Mohs micrographic surgery is a specialist removal method for non-melanoma skin cancers with high recurrence risk
- As an alternative for high-risk lesions, simple resection with adjunct radiotherapy has been recommended

53
Q

Describe what is meant by Bowen’s disease [1]

A

Bowen’s disease (also known as SCC in situ) occurs when the cancerous cells are confined to the epidermis.15 It can also progress into invasive SCC, so it is important to monitor and treat Bowen’s disease promptly.

54
Q

Describe the management of squamous cell skin cancer [3]

A

Surgical excision with 4mm margins if lesion < 20mm in diameter.

If tumour >20mm then margins should be 6mm.

Mohs micrographic surgery may be used in high-risk patients and in cosmetically important sites.

55
Q

Squamous skin cell cancer commonly mets to…[3]

A

The most commonly affected sites are lungs, liver and brain.

56
Q

Describe the differences in a good and bad prognosis for squamous skin cell cancer [4]

A

High-risk features include:

Size: >2mm deep or >20mm wide
Site: face, ear, genitals, hands, feet
Recurrence
Immunosuppressed individual
Poor differentiation (histologically)
Perineural invasion (histologically)
High tumour budding

Geeky medics^

57
Q

For Bowen’s disease, therapies such as [] or therapies like [] are first-line management

A

For Bowen’s disease, destructive therapies such as cryotherapy or topical therapies like 5-fluorouracil are first-line management.8

58
Q

Tx for serborrheic keratoses? [2]

A
  • reassurance about the benign nature of the lesion is an option
  • options for removal include curettage, cryosurgery and shave biopsy
59
Q

Name and describe this type of skin condition [3]

A

Junctional Naevi
Flat
Pigmented
Regular, symmetrical, static appearance

60
Q

Name and describe this type of skin condition [3]

A

Intradermal Naevi
* Protrude from the skin surface
* Pigmented or flesh coloured

61
Q

Name and describe this type of skin condition [1]

A

Blue Naevi
- solitary, bluish, smooth surfaced macule, papule or plaque. They are generally round or oval in shape.

62
Q

Name and describe this type of skin condition [1]

A

Dermatofibroma
- common benign fibrous skin lesions. They are caused by the abnormal growth of dermal dendritic histiocyte cells, often following a precipitating injury

63
Q

Describe the management options for Actinic Keratoses [4]

A

Management options include:
- 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
- Imiquimod can be used for lesions on the face and scalp when cryotherapy or other topical treatments cannot be used.