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Author: Camila K Janniger, MD, Clinical Professor of Dermatology, Clinical Associate Professor of Pediatrics, Chief of Pediatric Dermatology, New Jersey Medical School

Camila K Janniger is a member of the following medical societies: American Academy of Dermatology

Coauthor(s): Julie K Keck, MD, Assistant Professor of Clinical Pediatrics, Neurodevelopmental Pediatrician, Department of Developmental Pediatrics, Riley Hospital for Children; James D Korb, MD, Program Director, Department of Pediatrics, Children's Hospital of Orange County

Editors: Kevin P Connelly, DO, Clinical Assistant Professor, Department of Pediatrics, Division of General Pediatrics and Emergency Care, Virginia Commonwealth University; Medical Director, Paws for Health Pet Visitation Program of the Richmond SPCA; Pediatric Emergency Physician, Emergency Consultants Inc, Chippenham Medical Center; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine; Robert A Schwartz, MD, MPH, Professor and Head of Dermatology, Professor of Medicine, Professor of Pediatrics, Professor of Pathology, Professor of Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School; Merrily P M Poth, MD, Professor, Department of Pediatrics and Neuroscience, Uniformed Services University of the Health Sciences; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center

Author and Editor Disclosure

Synonyms and related keywords: dyshidrotic eczema, rash, pompholyx, dyshidrosis, cheiropompholyx, chiropompholyx, dyshidria, palmoplantar hyperhidrosis, dermatitis, pruritic vesicular eruption, acute and recurrent vesicular hand dermatitis

Background

Dyshidrotic eczema is a type of eczema (dermatitis) of unknown cause that is characterized by a pruritic vesicular eruption on the fingers, palms, and soles. The condition affects teenagers and adults and may be acute, recurrent, or chronic. A more appropriate term for this vesicular eruption is pompholyx, which means bubble. The clinical course of dyshidrotic eczema can range from self-limited to chronic, severe, or debilitating. The condition's unresponsiveness to treatment can be frustrating for the patient and physician.

The definition and causes of dyshidrotic eczema remain enigmatic.1 A lack of precision in definition has rendered accurate analysis of causation and comparisons of therapeutic strategies challenging. Some believe the terms pompholyx and dyshidrosis are obsolete and favor a new term, such as "acute and recurrent vesicular hand dermatitis."

Pathophysiology

The etiology of dyshidrotic eczema is unknown. The condition was inaccurately described in 1873 as dyshidrosis because of the clinical symptom of sweaty palms. The term dyshidrosis indicates a sweating abnormality, although histologic examination reveals no evidence of eccrine glandular involvement. Histologically, the vesicles are intraepidermal and spongiotic with little to no inflammatory changes. The more appropriate term for this vesicular eruption is pompholyx, which means bubble. Although strong reasons to use the term pompholyx have been noted, dyshidrotic eczema remains a commonly used term. A tiny percentage of individuals with the disorder note flares after ingesting metal salts, specifically chromium, cobalt, and nickel. Diets that eliminate these metal salts may rarely have some clinical benefit.

One causative study observed reactional pompholyx to interdigital-plantar intertrigos and endogenous reactions to metals or other allergens; however, an unexpected number of patients with so-called contact pompholyx, in which cosmetic and hygiene products play a preponderant role (compared with metals), were also reported.2

A genetic component to the development of dyshidrotic eczema may be involved in some patients. Dyshidrotic eczema has been described in few large families; no gene or locus had been identified.3 A genome-wide search in a large Chinese family identified a locus at chromosome 18q22.1-18q22.3, with a maximum 2-point logarithm of the odds (LOD) score of 3.61 at marker D18S1131 (theta = 0.00). Haplotype analyses showed the gene to be located within 12.07 cM region between markers D18S465 and D18S1362, which corresponds to 8 Mb.

Frequency

United States

Dyshidrotic eczema accounts for 5% of all cases of eczema of the hand.

Mortality/Morbidity

Dyshidrotic eczema has no associated mortality, although some severe cases can become debilitating.

Race

No racial predilection is reported.

Sex

The female-to-male ratio is 2:1.

Age

Peak incidence occurs in patients aged 20-40 years, although the disorder also occurs in teenagers and older patients.



History

Patients with dyshidrotic eczema first describe several hours of itching or burning sensations in their hands, feet, or both before the eruption develops. Tiny vesicles erupt first along lateral aspects of the fingers and then on the palms or soles. Palms and soles may be red and wet with perspiration. The vesicles usually persist for 3-4 weeks. Vesicle outbreaks may occur in waves. A photo-induced form of hand dermatitis resembling dyshidrotic eczema has been described.4

Physical

Physical examination performed early in the course of the flare reveals small (ie, 1-2 mm), clear, deep-seated vesicles without erythema erupting on the lateral aspects of fingers, the central palm, and plantar surfaces. The vesicles have been described as resembling tapioca pudding. Eruptions are usually bilateral and symmetric. Patients treated later in the course of dyshidrotic eczema may have unroofed vesicles with inflamed bases, possibly accompanied by peeling or rings of scale or lichenification. Transverse furrows can develop on the nail when eruptions occur in the periungual area, nail matrix, or both.

Causes

Although the etiology of dyshidrotic eczema remains undefined, suspected risk factors include stress, exposure to metal salts, allergic contact dermatitis, and female sex. Iannaccone et al (1999) cite exposure to intravenous immunoglobulin G (IVIG) as a possible risk factor.5



Other Problems to be Considered

Id reaction (ie, autoeczematization)
Pustular psoriasis
Primary fungal infection
Recurrent focal palmar peeling (previously termed keratolysis exfoliativa)
Dyshidrosiform bullous pemphigoid



Histologic Findings

The vesicles in patients with dyshidrotic eczema are intraepidermal and spongiotic.



Medical Care

In dyshidrotic eczema, typical first-line treatment includes high-strength topical steroids and cold compresses. Short courses of oral steroids are the second line of treatment for acute flares, and other immunosuppressants have also been tried. Corticosteroids are cornerstones of topical therapy, although calcineurin inhibitors may also be effective.6 Variable effects have been reported using oral administration of psoralen and subsequent exposure to long-wavelength ultraviolet light (PUVA) therapy. Topical photochemotherapy with 8-methoxypsoralen is probably as effective as systemic photochemotherapy or high-dose ultra violet type A-1 irradiation. For recalcitrant cases, corticosteroids are combined with immunosuppressants. A new evolving treatment seems to be the intradermal injection of botulinum toxin.

Topical khellin and natural sunlight therapy have been suggested for patients with recalcitrant palmoplantar pompholyx.7

Identification of the causes of stress and use of stress management techniques as adjuncts may be helpful in some patients.

Diet

Dyshidrotic eczema requires no dietary restrictions, although some patients have reported improvement by avoiding foods rich in heavy metal salts.

Activity

Dyshidrotic eczema may restrict activity; some refractory cases become debilitating. Some cases are precipitated by an environmental contact, which could also influence activities.



Dyshidrotic eczema treatment can be quite challenging because of the severe inflammatory process or because of frequent recurrences. Pharmacologic treatment begins with high-strength topical corticosteroids. In recalcitrant cases, systemic corticosteroids are the next line of treatment. Two recent case reports also note some success with other immunosuppressants (eg, methotrexate, mycophenolate mofetil).

The long-term efficacy of occlusive therapy with pimecrolimus (Elidel), a topical calcineurin inhibitor, has been reported in patients with severe dyshidrosiform hand and foot eczema.8 However, the authors recommend caution in the extended use of calcineurin inhibitors.

In March 2005, the US Food and Drug Administration (FDA) issued a public health advisory to inform healthcare professionals and patients about a potential cancer risk from use of pimecrolimus. This concern is based on information from animal studies, case reports in a small number of patients, and knowledge of how drugs in this class work. Human studies of 10 years or longer may be needed to determine if pimecrolimus administration is linked to cancer. In the meantime, this risk is uncertain, and the FDA advises pimecrolimus should only be used in patients in whom other prescription treatments have failed or cannot be tolerated. This information reflects the FDA’s preliminary analysis of data concerning this drug.

Drug Category: Corticosteroids

Topical corticosteroids are the first-line therapy. Steroid potency choice is based on the patient's response to treatment; however, the higher-strength steroids are usually necessary for disease control.

Drug NameClobetasol propionate (Temovate)
DescriptionA high-potency corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties.
Adult DoseApply to affected areas bid
Pediatric Dose<12 years: Not recommended
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; viral or fungal skin infections
InteractionsNone reported
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
PrecautionsMay suppress adrenal function in prolonged therapy

Drug NamePrednisone (Deltasone, Meticorten)
DescriptionA glucocorticoid readily absorbed from GI tract. Used as second-line pharmacologic treatment of dyshidrotic eczema. It is a potent anti-inflammatory agent that has salt-retaining properties and varied metabolic effects. Can modify immune response.
Adult Dose5-60 mg PO qd
Pediatric Dose0.5-2 mg/kg/d PO qd or divided bid/qid
ContraindicationsDocumented hypersensitivity; viral infection; peptic ulcer disease; hepatic dysfunction; connective tissue infections; fungal or tubercular skin infections; GI bleeding
InteractionsCoadministration with estrogens may decrease prednisone clearance; concurrent use with digoxin may cause digitalis toxicity secondary to hypokalemia; phenobarbital, phenytoin, and rifampin may increase metabolism of glucocorticoids (consider increasing maintenance dose); monitor for hypokalemia with coadministration of diuretics
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsAbrupt discontinuation of glucocorticoids may cause adrenal crisis; hyperglycemia, edema, osteonecrosis, myopathy, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, myasthenia gravis, growth suppression, and infections may occur with glucocorticoid use

Drug Category: Topical calcineurin inhibitor

These agents are topical immune suppressants that block early T-cell activation, degranulation of mast cells, and multiple cytokines.

Drug NamePimecrolimus (Elidel cream)
DescriptionFirst nonsteroid cream approved in the United States for mild-to-moderate atopic dermatitis. Derived from ascomycin, a natural substance produced by the fungus Streptomyces hygroscopicus var. ascomyceticus. Selectively inhibits production and release of inflammatory cytokines from activated T cells by binding to cytosolic immunophilin receptor macrophilin-12. The resulting complex inhibits phosphatase calcineurin, thus blocking T-cell activation and cytokine release. Cutaneous atrophy was not observed in clinical trials, a potential advantage over topical corticosteroids. Indicated only after other treatment options have failed.
Adult DoseApply topically to affected areas bid
Short-term and intermittent use only
Pediatric Dose<2 years: Not established
>2 years: Administer as in adults
Short-term and intermittent use only
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
PrecautionsPotential exacerbation of existing infection at site of application; may cause burning and irritation; caution with conditions that suppress the immune system (eg, AIDS, cancer); possible risk of lymph node or skin cancer based on animal studies and a small number of patients; may increase risk of viral infections; other adverse effects include headache, sore throat, flulike symptoms, fever, and cough



Further Inpatient Care

  • Inpatient care of dyshidrotic eczema is unnecessary.

Further Outpatient Care

  • Further outpatient care includes physician follow-up for treatment options.

Deterrence/Prevention

  • Decrease stress and avoid ingesting metal salts.

Complications

  • Complications include poor response to treatment, resulting in continued rash, pruritus, and possible superinfection.

Prognosis

  • The prognosis for patients with dyshidrotic eczema varies. Some individuals completely recover; some experience chronic unremitting dyshidrotic eczema.

Patient Education

  • Inform individuals with this disorder about the difficulty of achieving successful treatment.
  • For excellent patient education resources, visit eMedicine's Skin, Hair, and Nails Center. Also, see eMedicine's patient education article Eczema.



Medical/Legal Pitfalls

  • Failure to educate patients on the recurrent nature of dyshidrotic eczema



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Dyshidrotic Eczema excerpt

Article Last Updated: Sep 29, 2008