Derm 2 Flashcards

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1
Q

Pyoderma gangrenosum

  1. What is seen on biopsy?
  2. How is it managed?
A
  1. infiltrated neutrophils

2. oral steroids
due to risk of rapid progression

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2
Q

Dermatitis herpetiformis

  1. What is seen on biopsy?
  2. Other than gluten free diet what can be given?
A
  1. IgA deposition

2. dapsone

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3
Q

Fungal nail infections

  1. What is the most common cause?
  2. What is often the appearance of the nail?
  3. What investigation is done?
  4. How is it managed?
A
  1. trichophyton rubrum (90%)
  2. thickened, rough, opaque
  3. nail clippings / scrapping for culture
  4. oral turbinafine
    - > 6 weeks - 3 months if finger nail
    - > 3-6 months if toe nail

if candida is the cause then topical anti fungal or if severe oral itraconazole can be given

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4
Q

Impetigo

How is it managed regarding:

  1. limited disease
  2. extensive disease
  3. school exclusion
A
  1. hydrogen peroxide cream or topical fusidic acid
    - > topical mupirocin if resistant
  2. oral flucloxacillin
    (erythromycin if pen. allergic)
  3. > 48hrs after initiating ABx or wait until after lesions have healed
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5
Q

Molluscum contagiosum

  1. a) What causes it?
    b) Who is it most common in?
  2. What lesions are seen?
  3. How is it managed?
A
  1. a) molluschi contagiosum virus

b) children aged 1-4
2. “pink pearly papules” with central umbilicus

    • avoid sharing towels and clothes
    • only treat symptoms (e.g. topical corticosteroid for itch)
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6
Q

Pityriasis rosea

  1. What causes it?
  2. What CFs are seen?
  3. How is it managed?
A
  1. herpes hominis virus 7
  2. herald patch followed by smaller erythematous scaly patches
  3. self-limiting - should disappear after
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7
Q

Scabies

  1. What clinical features are seen?
  2. How is it managed?
A
    • intense itch
    • linear burrows on sides of fingers, interdigital web spaces and flexure surfaces of wrist
  1. 1st line: permethrin
    2nd line: malathion

apply and leave for 8-12 hours (24 hours if malathion) before washing off and repeat again in 7 days

treat everyone in household, wash all laundry (towels etc) on first day of treatment

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8
Q

Other than pre-malignant lesions (actinic keratoses + Bowen’s) and sunlight exposure what are the RFs for SCC?

A
  • smoking
  • immunosuppression
  • long standing leg ulcer (majorlin’s ulcer: malignancy arising from previously injured skin)
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9
Q

Actinic Keratoses

  1. What is seen?
  2. How can they be managed?
A
  1. small crusty scaly lesions on sun damaged skin
  2. flourouracil cream for 2-3 weeks +/- hydrocortisone after to reduce inflammation
    topical diclofenac can be used for very mild lesions
  • curettage + cautery
  • cryotherapy
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10
Q

What clinical features are seen in hereditary haemorrhagic telangiectasia?

A
  • recurrent epistaxis
  • telangiectases: possibly lips, oral cavity, fingers, nose
  • visceral lesions: for example gastrointestinal telangiectasia, pulmonary arteriovenous malformations (AVM), hepatic AVM, cerebral AVM, spinal AVM
  • family history: a first-degree relative with HHT
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11
Q

What can be given for hirsutism?

A
  • COCP

- topical eflornithine for face (but contraindicated in pregnancy)

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12
Q

Lichen sclerosus

  1. What CFs are seen?
  2. How is it managed?
  3. What is the patient at an increased risk of?
A
    • itchy, white plaques on genitalia
    • most commonly affects older women
      +/- painful intercourse or urination
  1. topical steroids + emollients
  2. vulval cancer
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13
Q
  1. What drugs can cause toxic epidermal necrolysis?

2. How is it managed?

A

1.

  • phenytoin
  • sulphonamides
  • allopurinol
  • penicillins
  • carbamazepine
  • NSAIDs
  1. IV immunoglobulins
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14
Q

Bullous pemphigoid v pemphigus vulgaris

  1. How can they be differentiated?
  2. What are their pathophysiologies and hence what is seen on biopsy?
  3. How are they treated?
A
    • bullous pemphigoid mucosal involvement less likely whereas pemphigus vulgaris likely to present with mucosal involvement (50-70% mouth ulcers)
    • bullous pemphigoid more likely to have itch and have intact blisters
  1. bullous pemphigoid: IgG and C3 deposited at the dermo-epidermal junction
    -> hence immunofluorescence shows linear band

pemphigus vulgaris: IgG invasion of desmosomes (glue holding epidermis together)
-> hence immunfluoresence shows chicken-wire appearance throughout epidermis

  1. oral / topical steroids
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