Acute and Emergency Dermatology Flashcards

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1
Q

What are the main cutaenous drug reactions that can occur?

A
  • Urticaria
  • Maculopapular rash
  • Lichenoid
  • Morbilliform rash
  • Erythroderma
  • SJS
  • Toxic epidermal necorlyisis
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2
Q

What type of drug reactions can present with penicillins?

A
  • Maculopapular rash
  • Urticaria
  • TEN
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3
Q

What are the most serious types of drug reactions?

A
  • Erythroderma
  • Toxic epidermal necrolysis
  • Drug-induced hypersensitivity syndrome
  • Steven-Johnson Syndrome
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4
Q

What is toxic epidermal necrolysis?

A

This is characterized by widespread subepidermal blistering and sloughing of more than 30% of the skin and a high mortality (30–50%). The internal epithelial surfaces (lung, bladder, gastrointestinal tract) are also involved. Multiorgan failure and sepsis often occur.

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5
Q

What are prodromal features of toxic epidermal necrolysis?

A

Precedes skin signs by 2-3 days

  • Fever > 39 C
  • Sore throat, dysphagia
  • Rhinorrhoea
  • Cough
  • Otalgia/conjunctivitis
  • Myalgia
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6
Q

What are features of toxic epidermal necrolysis?

A
  • Ulceration of mucous membranes
  • Rash
    • May start as macular, purpuric or blistering
    • Rapidly becomes confluent
    • Sloughing off of large areas of epidermis
    • Nikolsky’s sign may be positive
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7
Q

What can be complications of toxic epidermal necrolysis?

A
  • Dehydration and acute malnutrition
  • Infection - skin, mucous membranes, lungs, septicaemia
  • Acute respiratory distress syndrome
  • Gastrointestinal ulceration, perforation and intussusception
  • Shock and multiple organ failure including kidney failure
  • Thromboembolism/DIC
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8
Q

What groups of patients are more likely to develop TEN?

A

Those with HIV

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9
Q

What medications are associated with the development of TEN?

A
  • Sulfonamides: cotrimoxizole;
  • Beta-lactam: penicillins, cephalosporins
  • Anti-convulsants: lamotrigine, carbamazepine, phenytoin, phenobarbitone
  • Allopurinol
  • Paracetamol/acetominophen
  • Nevirapine
  • Nonsteroidal anti-inflammatory drugs (NSAIDs)
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10
Q

What mucosal surfaces are involved in TEN?

A
  • Eyes - conjunctivitis, less often corneal ulceration, anterior uveitis, panophthalmitis
  • Lips/mouth - cheilitis, stomatitis
  • Pharynx, oesophagus
  • Genital area and urinary tract — erosions, ulcers, urinary retention
  • Upper respiratory tract (trachea and bronchi)
  • Gastrointestinal tract — diarrhoea.
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11
Q

How would you manage toxic epidermal necrolysis/SJS?

A
  • Identify and stop culprit drug as soon as possible
  • Supportive therapy
  • Consider High dose steroids
  • Consider IV immunoglobulins
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12
Q

What is Steven’s Johnson syndrome?

A

A variant exists of TEN where the damage is restricted to the mucosal surfaces with milder bullous involvement of the skin (<10%). Both SJS and TEN are commoner in slow acetylators and very much commoner in those with HIV infection.

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13
Q

What are features of SJS?

A

Fever, malaise, arthralgia

Rash

  • Maculopapular, target lesions, blisters
  • Erosions covering <10% of skin surface

Mouth ulceration

  • Greyish white membrane
  • Haemorrhagic crusting

Ulceration of other mucous membranes

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14
Q

What percentage of the skin is affected in SJS?

A

<10%

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15
Q

What percentage of epidermal detachement occurs in TEN?

A

>30%

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16
Q

What scoring system could you use to determine mortality risk of someone with TEN/SJS?

A

SCORTEN Scoring system

  • Age >40
  • Malignancy
  • Heart rate >120
  • Initial epidermal detachment >10%
  • Serum urea >10
  • Serum glucose >14
  • Serum bicarbonate <20
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17
Q

What are long term complications of SJS/TEN?

A
  • Pigmentary skin changes
  • Scarring
  • Eye disease and blindness
  • Nail and hair loss
  • Joint contactures
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18
Q

What is the following?

A

Erythema multiforme - type of hypersensitivity reaction triggered most often by herpes simplex. clinically the lesions can be erythematous, polycyclic, annular or show concentric rings (‘target lesions’). The rash tends to be symmetrical and commonly affects the limbs, especially the hands and feet where palms and soles may be involved.

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19
Q

What could cause the following?

A

Hypersenstivity reaction caused by:

  • Herpes simplex virus
  • Other viral infections - e.g. Epstein–Barr virus (EBV)
  • Drugs - e.g. sulphonamide, anticonvulsants
  • Mycoplasma infection
  • Autoimmune rheumatic disease - e.g. SLE, polyarteritis nodosa
  • HIV infection
  • Wegener’s granulomatosis
  • Carcinoma, lymphoma.
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20
Q

What is the following?

A

Erythema multiforme - mucosal involvement around the mouth - this can lead to necrotic ulcers of the mouth and genitalia, and a conjunctivitis

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21
Q

What is meant by the minor form of erythema multiforme?

A

Erythematous well-defined round lesions appear on extensor surfaces of peripheries, palms, and soles andevolveat different stages into pathognomonic target lesions.

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26
Q

What are features of major erythema multiforme?

A

Features of minor with associated systemic upset and severe mucosal involvement

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27
Q

How long does erythema multiforme take to heal?

A

Up to 4 weeks

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28
Q

How would you manage erythema multiforme?

A
  • No treatment required
  • Consider steroids - provides relief but does not accelerate healing
  • Treat cause
  • Consider Aciclovir prophylaxis - if recurrent
29
Q

What are the features of erythema Multiforme?

A

Abrupt onset of up to 100s of lesions over 24 hours

  • Distal -> proximal
  • Palms and soles
  • Mucosal surfaces (EM major)
  • Evolve over 72 hours
    • Pink macules, become elevated and may blister in centre
    • “Target” lesions
30
Q

What is Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)?

A

A serious adverse systemic reaction to a drug typically occurring 2–6 weeks after initial exposure

31
Q

What are the characteristic features of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)?

A

Onset 2-8 weeks after drug exposure

  • Generalized mucocutaneous rash
  • Fever
  • Lymphadenopathy
  • Arthralgia
  • Pharyngitis
  • Periorbital oedema
  • Hepatosplenomegaly
32
Q

What may be found on investigation of bloods in someone with DRESS?

A
  • Eosinophilia
  • Deranged LFTs
33
Q

How would you manage someone with DRESS?

A
  • Stop causative drug
  • Symptomatic and supportive
  • Systemic steroids
  • +/- Immunosuppression or immunoglobulins
34
Q

What is staphylococcal scalded skin syndrome?

A

Widespread blistering disorder caused by toxin B released by staphylococcus

35
Q

When is staphylococcal scalded skin syndrome most common?

A

Childhood

36
Q

What types of patients is staphylococcal scalded skin syndrome commonly associated with?

A
  • Renal disease
  • Immunosuppression
37
Q

What desmosomal protein does toxin B secreted by staph target in staphylococcal scalded skin syndrome?

A

Desmoglein 1

38
Q

What are features of staphylococcal scalded skin syndrome?

A

Initial Staph. infection - Fever and irritability

  • Diffuse erythematous rash with skin tenderness
  • More prominent in flexures
  • Blistering and desquamation follows
39
Q

How would you differentiate SSSS from TEN?

A
  • Mucosal involvement only occurs in TEN
  • Skin biopsy shows a more superficial split in SSSS (intraepidermal) than in TEN (subepidermal)
40
Q

How would you manage someone with staphylococcal scalded skin syndrome?

A

IV antibiotics - Flucloxacillin

41
Q

What is urticaria?

A

Also known as hives or wheals, which is in basic terms oedema in the dermis

43
Q

What is the difference between urticaria and angioedema?

A

Urticaria is intensely itchy, whereas angioedema is rarely itchy

44
Q

What are features of an urticarial rash?

A

Develop acutely over a few minutes

  • Cutaneous swellings/weals
  • Intense pruritis
  • No surface change or scaling
  • Erythematous
    • If very acutely swollen, may appear flesh-coloured or whitish and people often mistake them for blisters.
45
Q

What are features of angioedema?

A

Soft tissue swelling (oedema) especially around the eyes, the lips and the hands but this is rarely itchy

46
Q

How quickly does urticaria develop?

A

Over a few minutes

50
Q

What is the pathogenesis of urticaria?

A

Degranulation of cutaneous mast cells which releases a number of inflammatory mediators (including histamine) which in turn make the dermal and sub-dermal capillaries leaky. In most cases the underlying cause is autoimmune (patients develop autoantibodies against the high-affinity IgE receptor α-subunit of the mast cell).

51
Q

What are phsyical causes of urticaria?

A
  • Cold
  • Deep pressure
  • Stress
  • Heat
  • Sunlight
  • Chemical irritants
52
Q

How would you manage someone with acute urticaria (<6 weeks)?

A
  • Treat underlying cause - remove cause
  • Avoid salicylates/opiates/NSAIDs - make it worse
  • Oral antihistamines - certrizine
53
Q

How would you manage angioedema?

A

If not hereditary:

  • IM adrenaline
  • IV steroids
54
Q

How would you manage someone with chronic urticaria?

A
55
Q

What is hereditary angioedema?

A

A rare autosomal dominant condition due to an inherited deficiency of C1 esterase inhibitor (C1-INH) which causes massive activation of the complement system, increased bradykinin levels and thus angio-oedema

56
Q

What are features of hereditary angioedema?

A
  • Attacks of non-itchy cutaneous angioedema - lasts for 72 hours
  • Recurrent abdo pain
  • NO URTICARIA
57
Q

How would you manage someone with an acute attack of hereditary angioedema?

A
  • C1 esterase inhibitor
  • FFP
  • Noveal agents - Icatibant, Ecallantaide
58
Q

What maintenance treatment would you use for hereditary angioedema?

A

Anabolic steroids - increase hepatic synthesis of C1 esterase inhibitor

59
Q

What is erythroderma?

A

A clinical state of inflammation/redness of all/nearly all of the skin. Sometimes called exfoliative dermatitis, but dermatitis is not alway present

60
Q

What are common causes of erythroderma?

A
  • Atopic eczema
  • Psoriasis
  • Drugs
  • Seborrhoeic eczema
  • Idiopathic
61
Q

What drugs can cause erythroderma?

A
  • Sulphonamides
  • Gold
  • Sulfonylureas
  • Penicillin
  • Allopurinol
  • Captopril
62
Q

What are features of erythroderma?

A

Widespread erythema affecting >/= 90% of the body

  • Skin feeling ‘tight’/itchy.
  • Longstanding - hair loss, ectropion of the eyelids and even nail shedding.
  • Systemic symptoms - malaise, pyrexia, widespread lymphadenopathy
64
Q

What are complications of erythroderma?

A
  • High-output cardiac failure from increased blood flow
  • Hypothermia from heat loss
  • Fluid loss by transpiration
  • Hypoalbuminaemia
  • Increased basal metabolic rate
  • ‘Capillary leak syndrome’
65
Q

What is the most severe complication of erythroderma?

A

Capillary leak syndrome

66
Q

What is capillary leak syndrome?

A

Inflammed skin releases large quantities of cytokine that cause generalised vascualr leakage. This can cause cutaenous oedema and acute lung injury

67
Q

How would you manage erythroderma?

A

Discuss with dermatologist

  • Treat cause
  • Keep very warm
  • Monitor vital signs regularly, particularly fluid balance
  • Correct biochem and albumin changes
  • Swabs - screen for secondary skin infection.
  • Bed rest
  • Bland emollient/mild topical steroid
  • Stop all non-essential drugs