Dermatology Flashcards

1
Q

What are the two descriptive terms for flat skin lesions?

What is the difference between these two?

A

Macules and Patches

The difference is their size

If less than or equal to 0.5cm it is termed a macule

Anything greater than 0.5cm is termed a patch

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2
Q

Smoothed raised lesions can be classified as cysts, nodules, papules and plaques.

Describe each of these

A

Cysts - A closed cavity or sac containing fluid or semisolid material

Nodules - A dermal or subcutaneous firm, well-defined lesion usually greater than 0.5 cm in diameter.

Papules - A discrete, solid, elevated body usually less than or equal to 0.5 cm in diameter. Papules are further classified by shape, size, color, and surface change.

Plaques - A discrete, solid, elevated body usually broader than it is thick, measuring more than 0.5 cm in diameter. Plaques may be further classified by shape, size, color, and surface change.

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3
Q

‘Surface change’ in skin can be classified as either crust or scale. What is the difference between these two?

A

Crust - A hardened layer that results when serum, blood, or purulent exudate dries on the skin surface. Crusts may be thin or thick and can have varying color.

Scale - results from excess stratum corneum (the most superficial layer of the skin) that accumulates in flakes or plates. Scale usually has a white or gray color.

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4
Q

What are the three types of fluid-filled skin lesions?

What are the differences between these three?

A

Bullae - fluid-filled blisters greater than 0.5 cm in diameter. Fluid can be clear, serous, hemorrhagic, or pus filled.

Vesicles - fluid-filled cavity or elevation less than or equal to 0.5 cm in diameter. Fluid may be clear, serous, hemorrhagic, or pus filled.

Pustules - A circumscribed elevation that contains pus. Pustules are usually less than or equal to 0.5 cm in diameter.

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5
Q

What layers of the skin do the following affect?

Bullous pemphigoid

Pemphigus vulgaris

Bullous impetigo

A

Bullous pemphigoiD - sub-dermal blisters

Pemphigus vulgaris - intra-epidermal blisters

Bullous impetigo - sub-corneal blisters

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6
Q

Pemphigus/Pemphigoid blisters are deep, lift up the entire epidermis and are resistant to rupturing

Pemphigus/Pemphigoid blisters are intra-epidermal and more prone to rupture, as such in clinics you may see them more as erosions rather than blisters

A

Pemphigoid blisters are deep and resistant to rupture

Pemphigus blisters are more prone to rupture and may present with erosions

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7
Q

When clinically investigating the nature of blisters, what would you do to confirm the following?

Infection

Porphyria

Contact dermatitis

Autoimmune

A

Infection - bacterial culture and microscopy, PCR, viral culture, serology

Porphyria - porphyrin studies

Contact dermatitis - patch testing

Autoimmune - biopsy with IMF

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8
Q

What is the most common of all the autoimmune blistering diseases?

A

Bullous pemphigoid

Incidence increases with age

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9
Q

What is the autoimmune pathophysiology of bullous pemphigoid?

A

IgG react with antigens in the basement membrane (BM) and with hemidesmosomes anchoring basal cells to BM

This results in local complement activation and tissue damage, with subdermal bullae forming

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10
Q

How is bullous pemphigoid treated

a) locally
b) generally?

What is the prognosis?

A

a) potent topical steroids
b) systemic steroids, tetracyclines, methotrexate

Chronic self-limiting condition, with most patients achieving remission in 3-6 months. Relapse is uncommon

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11
Q

How common is pemphigus vulgaris? What age range is most commonly affected?

A

Very uncommon, may never see it unless working as a dermatologist

Most commonly affects people in middle age

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12
Q

What is Nikolsky’s sign?

It is positive in Bullous Pemphigoid/Pemphigus vulgaris

A

Nikolsky’s sign is friability of a blister when rubbed with a wooden spatula

It is positive in PV but negative in BP

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13
Q

What are antibodies formed in response to in Pemphigus Vulgaris?

A

IgG antibodies are formed against desmoglein 3 (membrane protein that helps to maintain desmosome structure)

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14
Q

PV is a lot more difficult to treat than BP. How is PV treated?

What is the mortality associated with PV?

A

Locally - potent high dose topical steroids and topical anaesthetic creams

Systemicaly - prednisolone +/- another immunosuppressive agent

PV has a mortality rate of 10-20% in treated patients (used to be higher)

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15
Q

How common is Dermatitis Herpetiformis?

What other condition does it overlap with?

What age ranges are affected?

A

DH is very common

Overlaps with Coeliac Disease

Can affect all ages, majority are young adults

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16
Q

How does Dermatitis Herpetiformis present?

A

Widespread blisters and erosions

Particularly affects extensor aspects of arms, forearms and legs, buttocks, scapulae, face and scalp

Lesions are itchy - usually preceeds blisters and patients may present with excoriations

17
Q

In contrast to BP and PV, what type of immunoglobulin is seen in Dermatitis Herpetiformis?

A

Granular deposits of dermal papillary IgG

18
Q

What is a serious recognised complication associated with Dermatitis Herpetiformis?

NB - it’s very rare

A

lymphoma