Paeds Derm
Derm update 2024 - Dr Alicia Thornton
Psoriasis
Background
2% prevalence
Less common with darker skin
10% patients are < 10 years old
Related to metabolic syndrome
Relapsing / remitting
Predisposing
Strep infection
Family history
Skin Trauma
Psychological or physiological stress
Medications
Lithium, Interferon B, B blockers, Corticosteroid withdrawal, Anti-TNF
Alcohol
Types
Guttate
Chronic plaque
Palmplantar
Flexural
Genital
Sebopsoriasis
Nail
Pustular
Treatment
Topical steroids
Wet dressings once or twice daily
Bland emolients (cream not ointment)
Keratolytics (low concentration salicylic acid 2 to 3%)
Coal tar creams
UVB phototherapy
Systemic agents
Methotrexate, Cyclosporine, Acitretin, Newer
Biologics
Adalimumab 4 years +
Ustekinumab 6 years +
Granuloma Annulare
Background
Common in children
Often asymptomatic
Variants
Localised
Generalised on trunk + extremities
Subcutaneous - nodules - pretibial, hands, buttocks, scalp, feet,
Perforating - crusting, ulcers, dorsal hands and fingers
Predisposing
Family history
Diabetes
Infections
Vaccinations
Skin trauma
Treatment
Potent steroids (Diprosone 0.05% ointment - better penetration
Occlusion
Steroids then white cotton sock then spray bottle with water over affected areas
Tubifast cut to size
Intralesional steroid injections 6 to 8 weekly
Pimecrolimus or tacrolimus 0.1% compounded ointment
Can be useful on face
Use when lesions have started to thin after potent steroids
UV phototherapy
Systemics agents - Plaquneil, Pred, Minocycline, Isoretinoin, Dapsone, MTX
Prognosis
50% resolve spontaneously by 2 years, more likely if localised lesions only
Pityriasis Roasea
Extensive exanthem
Preceded with herald patch 1 to 2 weeks
Age 10 to 35
Common in Autumun and Spring
Linked to HHV6 and 7 - often asymptomatic
Pink palpable plaque with trailing collarette of scale
Christmas tree distribution (followes lines of cleavage)
Self resolves 6 to 14 weeks
Mid-potency steroids and emolients
Erythromycin 2 to 4 weeks
UVB or sun exposure
Antihistmamine
Pityriasis Lichenoides
Clonal T- cell disorder
Thought to be triggered by virus
Recurrent crops of spontaneous regressing scaly papules
Can be itchy or not, can be sensitive and stingy
Range from acute form
Acute to chronic PLEVA / PLC
Rare cases of progression to cutaneous T cell lymphoma
6 to 12 monthly monitoring
Mid-potency topical steroids, coal tar, erythromycin, UVB, short course prednisolone, methotrexate
Lichen Nitidus
Fine pin point papules skin coloured
Flexural surfaces of arms
Subtype lichen planus
Topica lsteroids
Lichen Striatus
Self limited dermatitis in Blaschkoid unilateral distribution
Age 4 months to 15 years
Sudden onset
Regressed over 6 to 12 months
Dut to somatic mosaicism +/- viral trigger
Nail involvement
Usually asymptomatic
Topical steroids don’t generally work
Vitiligo
Acquired autoimmune depigmentation condition
Loss of melanocytes
2% prevalence
Bimodal < 10 and >30 years
Predisposing
Family history
Autoimmunity
Koebnerisation
Metastatic melanoma + treatment
Consider skin biopsy
FBC, UEC, LFT, Iron studies, CRP, ESR
B12, ANA, ENA, TFT + antibodies, coeliac serology, BSL, Urine glucose
HBV, HCV, HIV, QF gold, Strongyloides
Chronic and prone to relapse
Support groups
Treatment
Camouflage
Sun protection
Topical steroids e.g. Methylprednisolone 0.1% daily (Advantan) alternate weeks
Daivobet ointment
Compounded tacrolimus 0.03% or 0.1%
UV phototherapy
Topical JAK inhibitors
Systemic agents
Depigmentation therapies