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Evidence Levels: A Double-blind study B Clinical trial ≥ 20 subjects C Clinical trial < 20 subjects D Series ≥ 5 subjects E Anecdotal case reports
The hands and feet are essential tools in daily activities. The bipedal gait and manual activity of homo sapiens result in high exposure of these areas to numerous allergens and irritants. The palmar and plantar skin have a similar skin structure with a thick corneal layer, thus creating a special situation regarding penetration characteristics of topical therapies.
Cases of hand and foot eczema can be classified regarding their etiology, clinical presentation, and chronicity. Hand and foot eczema can be triggered by endogenous factors, such as atopy or contact to exogenous factors, such as irritants or allergens.
A clinical classification of the disease is most commonly based on morphology, ranging from pompholyx and dyshidrotic eczema to hyperkeratotic and fissured skin lesions. The clinical presentation is quite variable, and transitional as well as overlapping forms are often present. Pruritus and pain are frequent symptoms, especially if fissures are present. Secondary infection is common.
The acute, recurrent, and persistent course of the hand and foot eczema will largely determine the choice of treatment modalities.
Diagnostic procedures should be performed either to exclude the common differential diagnoses of hand and foot dermatitis such as dermatomycoses and psoriasis, or to reveal potential trigger factors of irritant and allergic contact eczema. The presence of lesions on both hands and feet is associated with chronic and more severe hand eczema, as well as a hyperkeratotic subtype of hand eczema.
Before starting any treatment, avoidance strategies and measures for known irritants and allergens should be employed. This may include a nickel-free diet and complete cessation of smoking for nickel-sensitized patients. Moreover, patient education programs and adherence improving techniques are helpful components of an effective management system.
Possible treatment options include topical agents, ultraviolet (UV) phototherapy, and systemic therapy. Dry and fissured skin lesions are best treated with highly lipophilic ointments, possibly combined with occlusive or semi-occlusive dressings to increase penetration. Keratolytic agents such as urea or salicylic acid are helpful in hyperkeratotic eczema, whereas moist and oozing skin may benefit from hydrophilic creams or gels. Desiccative agents have shown value in dyshidrotic forms of eczema. Antiseptics should be considered to avoid superinfection, especially in erosive or fissured lesions.
Topical corticosteroids of medium to high potency are the mainstay of all topical therapies of hand eczema. The topical calcineurin inhibitor tacrolimus may also be effective, especially for long-term treatment, but should not be combined with UV therapy. Pimecrolimus has shown less efficacy.
Calcipotriol ointment may show beneficial effects in chronic hand eczema, especially in the hyperkeratotic subtype, and may reflect a topical steroid-sparing alternative.
Adjuvant use of oral antihistamines has demonstrated only a slight effect on pruritus. Oral antibiotics, such as first generation cephalosporins, may be added in case of severe bacterial infection.
Psoralen–UVA (PUVA) therapy is the most effective UV-light treatment option for chronic, recurrent hand and foot eczema. UVA phototherapy or narrowband UVB (NB-UVB) phototherapy may also be useful.
Systemic treatment is frequently required in severe, refractory, or persistent hand and foot eczema. Systemic corticosteroids are recommended for short-term use only. Prednisone 0.5–1.0 mg/kg/day tapered over 2 weeks is a typical regimen. Systemic retinoids such as alitretinoin or acitretin are helpful if pregnancy prevention programs are followed strictly. Classic immunosuppressants such as methotrexate, azathioprine , and mycophenolate mofetil have been tried successfully. Ciclosporin may be especially useful in atopic hand eczema, and is approved in many countries for severe atopic dermatitis. Interestingly, a case has also been reported of improvement with oral apremilast.
New emerging therapies include dupilumab , a monoclonal antibody blocking the IL-4/IL-13 pathway. Topical Janus kinase (JAK) inhibitors such as delgocitinib may improve chronic hand eczema despite its subtype, and should be useful in therapy-refractory chronic hand eczema. Oral JAK inhibitors will undoubtedly be useful for hand eczema in the future.
Intradermal localized botulinum toxin A will reduce sweating and may therefore be helpful as adjuvant therapies in dyshidrotic forms.
Agner T, Aalto-Korte K, Andersen KE, et al. J Eur Acad Dermatol Venereol 2017; 31: 828–32.
About 30% of all hand eczema patients presented with concomitant foot eczema. Hyperkeratotic lesions, a long duration, and high severity of the hand eczema were associated with combined foot involvement.
Boonstra MB, Christoffers WA, Coenraads PJ, et al. J Eur Acad Dermatol Venereol 2015; 29: 940–7.
The retrospective study including 1571 patients revealed nickel sulfate, cobalt, fragrances, and preservatives as the most common causative allergens in hand eczema. Contact allergy was more prevalent in patients with recurrent vesicular hand eczema.
Elsner P, Agner T. J Eur Acad Dermatol Venereol 2020; 34 (Suppl 1): 13–21.
Broad review on the treatment of hand eczema and new emerging therapeutic targets.
Worm M, Bauer A, Elsner P, et al. Br J Dermatol 2020; 182(5): 1103–10.
A total of 91 patients with chronic hand eczema were randomized to receive delgocitinib ointment or vehicle for 8 weeks. Of the patients receiving delgocitinib, 46% achieved a Physician’s Global Assessment of disease severity (PGA) of clear or almost clear with 2-point reduction from baseline compared with 15% receiving placebo ( p = 0.0009). Additionally, mean Hand Eczema Severity Index (HECSI) score was lower with delgocitinib than with placebo (13.0 vs. 25.8; p = 0.0003).
Schnopp C, Remling R, Mohrenschlager M, et al. J Am Acad Dermatol 2002; 46: 73–7.
In 16 patients with dyshidrotic hand eczema, topical tacrolimus 0.1% ointment applied twice daily showed an efficacy comparable to 0.1% mometasone furoate ointment after 4 weeks.
Hordinsky M, Fleischer A, Rivers JK, et al. Dermatology 2010; 221: 71–7.
Less than 30% of 652 patients showed improved skin and reduced itch upon topical therapy with pimecrolimus 1% cream applied twice daily with overnight occlusion over 6 weeks.
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