Acute and Emergency Dermatology Flashcards

1
Q

What are the normal functions of the skin and consequences of failure?

A

Mechanical barrier to infection - sepsis
Temperature regulation - hypo or hyperthermia
Fluid and electrolyte balance - protein + fluid loss, renal impairment and peripheral vasodilation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is erythroderma?

A

A descriptive term rather than diagnosis
Any inflammatory skin disease affecting more than 90% of total skin surface

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the causes of erythroderma?

A

Psoriasis, eczema, drugs, cutaneous lymphoma, hereditary disorders and unknown

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the principles of management for erythroderma?

A

Remove any offending drugs, careful fluid balance, good nutrition, temp. regulation, emollients, oral and eye care, anticipate and treat infection, manage itch and disease specific therapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is a type of mild drug reactions affecting the skin?

A

Morbilliform exanthem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are some types of severe drug reaction affecting the skin?

A

Erythroderma, Stevens Johnson Syndrome/ Toxic epidermal necrolysis and DRESS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe Stevens Johnson syndrome/ toxic epidermal necrolysis

A

2 conditions which are part of the same spectrum - TEN is more severe with more than 30% of skin affected
Rare
Secondary to drugs
Can be delayed onset

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What drugs can Stevens Johnson Syndrome/ Toxic Epidermal Necrolysis be secondary to?

A

Antibiotics, anticonvulsants, allopurinol and NSAIDs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the surface of epidermal detachment in SJS and TEN?

A

SJS - Under 10% epidermal detachment
SJS-TEN overlap - 10-30%
TEN - over 30%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the clinical features of SJS?

A

Fever, malaise, arthralgia, rash ( macropapular, target lesions and blisters), mouth ulceration and ulceration of other mucous membranes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Describe toxic epidermal necrolysis presentation

A

Often presents with prodromal febrile illness
Ulceration of mucous membranes
Rash - may start as macular, purpuric or blistering, rapidly becomes confluent and sloughing off large areas of epidermis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the management for SJS and TEN?

A

Identify and stop culprit drug as soon as possible
Supportive therapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How is prognosis of SJS/ TEN calculated?

A

SCORTEN score
Age >40, malignancy, heart rate >120, initial epidermal detachment >10%, serum urea >10, serum glucose >14 and serum bicarbonate <20

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the long term complications of SJS or TEN?

A

Pigmentary skin changes, scarring, eye disease + blindness, nail + hair loss and joint contractures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is erythema multiforme?

A

Hypersensitivity reaction usually triggered by infection - most commonly HSV then mycoplasma pneumonia
Abrupt onset up to 100s of lesions on body over 24hrs
Self limiting and resolves in 2 weeks
Symptomatic and treat underlying cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the presentation of erythema multiforme?

A

Distal to proximal
Palms and soles
Mucosal membranes
Evolves over 72hrs - pink macules and my blister in centre

17
Q

What does DRESS stand for?

A

Drug reaction with eosinophilia and systemic symptoms

18
Q

Describe DRESS

A

Mortality up to 10%
Onset between 2-8 weeks after drug exposure
Fever and widespread rash
Eosinophilia and deranged liver function
Lymphadenopathy and other organ involvement

19
Q

What is the treatment for DRESS?

A

Stop causative drug
Symptomatic and supportive
Systemic steroids
Maybe immunosuppression or immunoglobulins

20
Q

What are the clinical features of pemphigus?

A

Antibodies targeted at desmosomes
Skin - flaccid blisters and rupture very easily
Common sites - face, axillae and groins
Nikolsky’s sign may be +

21
Q

Where else can pemphigus also affect?

A

Commonly affects mucous membranes
Ill defined erosions in mouth
Can also affect eyes, nose and genital areas

22
Q

How is pemphigus and pemphigoid diagnosed?

A

Immunofluorescence skin biopsy is gold standard

23
Q

Describe pemphigoid

A

Antibodies directed at dermo-epidermal junction
Intact epidermis forms roof of blisters
Blisters are usually tense and intact

24
Q

What are the main characteristics of pemphigus?

A

Uncommon, middle age, blisters are fragile, mucous membranes usually affected, may be unwell if extensive and treat with systemic steroids + dress erosions

25
What are the main characteristics of pemphigoid?
Common, elderly patients, bisters often intact + tense, patients fairly well systemically and topical steroids may be sufficient if localised
26
What are the common causes of erythrodermic psoriasis and pustular psoriasis?
Infection and sudden withdrawal of oral steroids or potent topical steroids
27
What is erythrodermic psoriasis and pustular psoriasis?
Rapid development of generalised erythema and maybe cluster of pustules Fever and elevated WCC Exclude underlying infection, bland emollient and avoid steroids Often need systemic therapy
28
Describe eczema herpeticum
Disseminated HSV on background of uncontrolled eczema Monomorphic blisters and punched out erosions Generally painful and not itchy Fever and lethargy
29
What is the treatment for eczema herpeticum
Treatment dose acyclovir Treat secondary infection Mild topical steroid if needed to treat eczema Possible ophthalmology input In adults consider underlying immunocompromise
30
Describe staphylococcal scalded skin syndrome
Common in children and immunocompromised adults Initial staph infection Diffuse erythematous rash with skin tenderness More prominent in flexures Blistering and desquamation follows Fever and irritability
31
What is the treatment for staphylococcal scalded skin syndrome?
Admission for IV antibiotics initially and supportive care Generally resolves over 5-7 days with treatment
32
What is the pathophysiology of staphylococcal scalded skin syndrome?
Staphylococcus produces toxin which targets desmoglein 1
33
How does urticaria present?
Weal, wheal or hive - central swelling surrounded by erythema and dermal oedema. Itching and sometimes burning. duration 1-24hrs Angioedema - deeper swelling of the skin or mucous membranes
34
What are the causes of acute urticaria?
Idiopathic Infection - viral usually Drugs - IgE mediated Food - IgE mediated
35
What is the treatment of acute urticaria?
Less than 6 week history Oral antihistamine Short course oral steroid may be a benefit Avoid opiates and NSAIDs if possible
36
What are the causes of chronic urticaria?
More than 6 week history Autoimmune/ Idiopathic Physical Vasculitis Rarely type 1 hypersensitivity reaction
37
What is the management for chronic urticaria?
Standard dose non-sedating H1 antihistamine Then move up to higher dose and add in second antihistamine Consider second line agent - anti-leukotriene and tranexamic acid Consider immunomodulant - omalizumab