Dermatology: Emergencies Flashcards

1
Q

State some dermatological emergencies

A
  • Eczema herpeticum
  • Necrotising fasciitis
  • Staphylococcal scalded skin syndrome
  • Urticaria, angioedema & anaphylaxis
  • Stevens-Johnson syndrome
  • Toxic-epidermal necrolysis
  • Erythroderma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

For eczema herpeticum, discuss:

  • What it is
  • Who is it more commonly seen in
  • Typical presentation
  • Management
  • Potential complications
A
  • Skin infection caused by HSV 1 or 2
  • More commonly seen in children with eczema
  • Presentation of rash:
    • Widespread
    • Rapidly progressing
    • Erythematous
    • Painful
    • ?itchy
    • Vesicles containing pus (may see punched out ulcers if these have burst)
  • Management:
    • Aciclovir (mild or moderate may be treated with PO but severe treated with IV. **PASSMED says should be admitted for IV aciclovir)
  • Complications:
    • Potentially life-threatening
    • Bacterial superinfection
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

For Staphylococcal scaled skin syndrome, discuss:

  • What it is/cause
  • Who it usually affects
  • Presentation
  • Potential consequences
  • Management
A
  • Skin infection with type of Staphylococcus that produces epidermolytic toxins that cause skin breakdown
  • Children <5yrs
  • Presentation:
    • Start with generalised patches erythema on skin
    • Skin then looks thin & wrinkled
    • Formation of bullae
    • Burst, leave sore erythematous skin below
    • Nikolsky sign positive
    • Systemic symptoms: fever, lethargy, irritability, dehydration
  • Potential consequences: sepsis → death
  • Management:
    • Admission to hospital (under care dermatology)
    • IV antibiotics
    • Analgesia
    • Close monitoring of fluid balance and electrolytes (and fluids if required)

*Resolves in ~5-7 days

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

What is necrotising fasciitis?

There are numerous types of necrotising fasciitis; explain difference and state which is more common

A
  • Necrotising fasciitis is a rapidly spreading infection of deep fascia with secondary tissue necrosis
  • Types:
    • Type 1: polymicrobial with mixed anaerobes & aerobes (MOST COMMON)
    • Type 2: monomicrobial- caused by group A haemolytic streptococcus/Streptococcus pyogenes
    • Type 3: rare monomicrobial due to marine mircrobes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

State some risk factors for necrotising fasciitis

A
  • Compromised skin integrity: recent trauma, burns or soft tissue infection
  • Diabetes mellitus
    • Particularly if on SGLT2 inhibitors
  • Immunosuppression
  • IV drug use
  • Abdominal surgery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What site is most commonly affected by necrotising fasciitis?

A

Perineum (Fournier’s gangrene- necrotising fasciitis affecting genitals and perineal area)

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

Describe typical presentation of necrotising fasciitis

A
  • Acute onset
  • Severe pain
  • Erythema
  • Swelling
  • Blistering
  • Systemical unwell
  • Necrotic skin (late sign)
  • Crepitus (subcutaneous emphysema) (late sign)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Discuss the management of necrotising fasciitis

What is the mortality?

A

Urgent admission to hospital:

  • Urgent surgical debridement (may even need amputation)
  • IV abx

Average mortality= 10-40% (BMJ)

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

What is SJS/TEN?

A

SJS and TEN are considered two ends of spectrum of severe epidermolytic adverse cutanous drug reactions.

  • SJS <10% body surface area involved
  • TEN >30% of body surface involved

*(when in-between 10 and 30% conditions overlap)

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

Incidence of SJS/TEN is higher in what patients?

A

HIV positive patients

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

Drugs are the most common cause of SJS/TEN (infections are occasionally reported as the sole cause); state some common drugs that cause SJS/TEN

A
  • Allopurinol
  • Sulphonamides
  • Antibiotics (penicillin’s)
  • Anticonvulsants (lamotrigine, carbamazepine, phenytoin)
  • NSAIDS (oxicam-type)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Discuss the clinical features of SJS/TEN

A
  • Onset within 2 months of commencing causative drug
  • Painful, dusky erythema with blisters & erosions
  • Rapidly progress into confluent erythema with sheet-like epidermal detachment
  • Nickolsky sign (epidermis detached by mechanical pressure)
  • Mucosal involvement (more common in SJS [at least 2 mucosal sites] than in TEN)
  • Systemically unwell (fever, tachycardia etc..)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Diagnosis of SJS/TEN is made clinically, but how is it confirmed?

A

Biopsy

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

Discuss the management of SJS/TEN

A

Need early recognition and admission to hospital:

  • Stop causative drug
  • Supportive care best delivered in ICU or burns unit (e.g. fluids, electrolyte management, wound managemet)
  • Analgesia
  • IV immunoglobulins
  • Ophthalmology review for eye involvement
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Discuss the mortality of SJS and TEN

A
  • SJS= 5-12%
  • TEN= >30%

Death often due to sepsis, electrolyte imbalance or multi-system organ failure

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

What is erythroderma (also called exfoliative dermatitis)?

State some potential causes

Describe typical presentation

A
  • Rash affecting at least 90% of skin surface (also called exfoliative dermatitis; ‘exfoliative’ describes the skin peeling which is found
  • Causes:
    • Previous skin disease (eczema, psoriasis)
    • Drugs (e.g. sulphonamides, allopurinol, pencillin)
    • Lymphoma
    • Idiopathic
  • Presentation:
    • Inflamed, oedematous, scaly skin
    • Lymphadenopathy common
    • Systemically unwell
17
Q

Discuss the management of erythroderma

A

Urgently discuss with dermatologist, may need admitting

  • Treat underlying cause
  • Emollients & wet wraps to maintain skin moisture
  • Topical steroids to relieve inflammation
18
Q

State some potential complications of erythroderma

Discuss the prognosis of erythroderma

A

Complications

  • Secondary infection
  • Fluid loss & electrolyte imbalance
  • Hypothermia
  • High output cardiac failure and leaky capillary syndrome

Mortality depends on underlying cause and ranges from 20-40%