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Chapter: Paediatrics: Dermatology

Paediatrics: Papular rashes (1)

Acute urticaria affects 10% of the population at some time.

Papular rashes (1)

 

Urticaria (hives)

 

Acute urticaria affects 10% of the population at some time.

 

Pathophysiology 

Adverse stimulus l mast cell degranulation l histamine release l localized vasodilatation and ‘rise’capillary permeability.

 

Causes

 

Usually idiopathic or triggered by recent viral infection. Other causes in-clude:

   Allergens (e.g. drugs, foods, inhalants, insect bites).

 

   Trauma (physical urticarias), e.g. dermographism due to light skin trauma (commonest), pressure, cold, heat, sunlight.

 

Chronic urticaria (defined as acute urticaria not resolving after 2mths) is idiopathic in >90%, but may be caused by:

·  Chronic bacterial, fungal (e.g. oral Candida), or parasitic infection.

 

·  Rarely, ingested food dyes.

 

Presentation

 

   Rapidly developing erythematous eruption with raised central white wheals and occasionally local purpura.

 

   Any part of body can be affected and often itchy.

 

   Lesions last 4–24hr.

 

   May have associated fever and arthralgia (serum sickness).

 

Investigation

 

Apart from good history investigation is usually not necessary. Skin prick testing is rarely helpful. If chronic, consider:

   FBC;

 

   throat swab (streptococcus);

 

   urine culture;

 

   exclude threadworms;

 

   food and symptom diary.

 

Treatment

 

   Oral antihistamines.

 

   Oral prednisolone, short course if severe.

 

Avoid triggering factors, e.g. ingested food dyes and non-steroidal drugs.

Angioedema

 

Variant of urticaria with significant swelling of subcutaneous tissues, often involves lips, eyelids, genitalia, tongue, or larynx. If severe, may cause acute upper or lower respiratory tract obstruction and may be life-threatening.

 

Causes 

As for urticaria. Hereditary angioedema is a rare AD condition caused by active C1-esterase inhibitor deficiency.

 

Investigations and management 

As for urticaria. If hereditary angioedema is suspected then measure serum C4 complement level initially.

 

Treatment for severe angioedema

 

Give facial oxygen.

 

IM 0.1mL/kg adrenaline 1:10 000.

 

IM/IV hydrocortisone 12-hourly.

 

Nebulized salbutamol.

 

Prophylaxis

 

In severe and recurring cases of hereditary angioedema, tranexamic acid or anabolic steroids (e.g. danazole boosts liver production of C1-esterase inhibitor) are effective, but the latter is rarely used in childhood due to its androgenic effects.

 

Molluscum contagiosum

 

Common pox virus infection affecting infants and young children. Presentation

 

Pink umbilicated (central dimple) papules. Usually affects moist areas, but can occur anywhere. Exacerbated by active eczema or topical steroids.

 

Treatment

 

None if uncomplicated as usually spontaneously resolves within a year. If problematic:

·Treat any associated eczema.

 

Pinch forcep liquid nitrogen cryotherapy.

 

Lesion curettage.

 

Application of benzoyl peroxide 5% daily.

 

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