Emergency dermatology Flashcards

1
Q

List some causes of urticaria, angioedema and anaphylaxis

A
Idiopathic
Food
Drugs
Insect bites
Contact - latex
Viral infection
Parasitic infection
Autoimmune 
Hereditary
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2
Q

Describe the pathophysiology of urticaria

A

Due to a local increase in permeability of capillaries and small venules. Large number of inflammatory mediators (prostaglandins, leukotrienes and chemotactic factors) play a role but histamine derived from skin mast cells appears to be major mediator
Local mediator release from mast cells can be induced by immunological and non-immunological mechanisms

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3
Q

How does urticaria present

A

Swelling involving the superficial dermis, raising the epidermis - itchy wheals

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4
Q

How does angioedema present?

A

Deeper swelling involving the dermis and subcutaneous tissue - swelling of the tongue and lips

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5
Q

How does anaphylaxis present?

A

Bronchospasm
Facial and laryngeal oedema
Hypotension
Can initially present with urticaria and angioedema

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6
Q

What is the management of urticaria?

A

Antihistamines

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7
Q

What is the management of angioedema?

A

Corticosteroids

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8
Q

What is the management of anaphylaxis?

A

Adrenaline
Corticosteroids
Antihistamines

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9
Q

What is a complication of angioedema and anaphylaxis

A

Asphyxiation and death

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10
Q

What is erythema nodosum

A

A hypersensitivity response to a variety of stimuli

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11
Q

What causes erythema nodosum

A
Group A beta haemolytic streptococcus 
Primary tuberculosis
Pregnancy 
Malignancy
IBD
Chlamydia
Leprosy
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12
Q

How does erythema nodosum present

A

Discrete tender nodules which may become confluent
Usually appear on the shins
As they resolve they become bruise like in colouration
Lesions continue to appear for 1-2 weeks
Lesions do not ulcerate and resolve without atrophy or scarring

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13
Q

Describe erythema multiforme

A

Often of unknown cause - herpes simplex virus may precipitate it
Self limiting acute inflammatory condition
Mucosal involvement is absent/limited to one mucosal surface only

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14
Q

Describe Steven Johnson syndrome

A

Characterised by mucocutaneous necrosis with at least 2 mucosal sites involved
Skin involvement may be limited or extensive
Drugs or combinations of infections or drugs may be associated
Epithelial necrosis with few inflammatory cells seen on histopathology.
May have a prodromal illness

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15
Q

Describe toxic epidermal necrosis

A

Usually drug induced

Acute severe disease characterised by extensive skin and mucosal necrosis accompanied by systemic toxicity

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16
Q

Describe the management of TEN and SJS

A

Early recognition and call for help

Full supportive care to maintain haemodynamic equilibrium

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17
Q

What is the mortality rate for SJS

A

12%

18
Q

What is the mortality rare for TEN

A

> 30%

19
Q

What is death from SJS and TEN usually due to?

A

Sepsis, electrolyte abnormalities or multiorgan failure

20
Q

Describe acute meningococcaemia

A

A serious communicable infection transmitted via respiratory secretions, bacteria get into the circulating blood

21
Q

What organisms cause acute meningococcaemia

A

Gram negative diplococcus Neisseria meningitides

22
Q

Describe the presentation of acute meningococcaemia

A

Features of meningitis - headache, fever, neck stiffness
Features of septicaemia - Hypotension, fever, myalgia
Typical rash - non blanching purpuric rash on trunk and extremities which may be preceded by a maculopapular rash and can rapidly progress into ecchymoses, haemorrhagic bullae and tissue necrosis

23
Q

What is the treatment of acute meningococcaemia

A
Antibiotics (eg. benzylpenicillin)
Prophylactic antibiotics (eg. rifampicin) for close contacts (ideally within 14 days of exposure)
24
Q

What are the complications of acute meningococcaemia

A

DIC
Septic shock
Multiorgan failure
Death

25
Q

What is erythroderma

A

Exfoliative dermatitis involving at least 90% of the skin surface

26
Q

List some causes of erythroderma

A

Previous skin disease - eczema and psoriasis
Lymphoma
Drugs - sulphonamides, gold, sulphonlyureas, penicillin, allopurinol, captopril
Idiopathic

27
Q

How does erythroderma present?

A

Skin appears inflamed, oedematous and scaly

Systemically unwell with malaise and lymphadenopathy

28
Q

How is erythroderma treated?

A

Treat the underlying cause
Emollients and wet wraps
Topical steroids to reduce inflammation

29
Q

What are the complications of erythroderma

A
Secondary infection 
Fluid loss
Electrolyte imbalance
Hypothermia
High output cardiac failure 
Capillary leak syndrome
30
Q

Describe the prognosis for erythroderma

A

Depends on underlying diagnosis - 20-40%

31
Q

Describe eczema herpeticum

A

Widespread eruption - serious complication of eczema

32
Q

What causes eczema herpeticum

A

Herpes simplex virus

33
Q

Describe the presentation of eczema herpeticum

A

Extensive crusted papules, blisters and erosions

Systemically unwell with fever and malaise

34
Q

Describe the management of eczema herpeticum

A

Antivirals

Antibiotics for any secondary bacterial infection

35
Q

List the complications of eczema herpeticum

A

Herpes hepatitis
Encephalitis
DIC
Rarely death

36
Q

Describe necrotising fasciitis

A

A rapidly spreading infection of the deep fascia with secondary tissue necrosis

37
Q

What causes necrotising fasciitis

A

Group A haemolytic streptococci

Mixture of anaerobic and aerobic bacteria

38
Q

What are the risk factors for necrotising fasciitis

A

Abdominal surgery
Medical comorbidity - diabetes and malignancy
Although 50% occur in healthy individuals

39
Q

Describe the presentation of necrotising fasciitis

A

Severe pain
Erythematous, blistering and necrotic skin
Systemically unwell with fever and tachycardia
Presence of crepitus - subcutaneous emphysema

40
Q

What may an x-ray show in necrotising fasciitis

A

Soft tissue gas

41
Q

How is necrotising fasciitis managed

A

Urgent referral for surgical debridement

IV antibiotics

42
Q

What is the prognosis of necrotising fasciitis

A

Mortality up to 76%