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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
Darier disease (DD) is inherited in an autosomal dominant manner with an incidence of 1:25,000–1:100,000. Patients begin to develop malodorous, greasy, and crusted hyperkeratotic papules in seborrheic and flexural areas around puberty. DD is caused by mutations in the ATP2A2 gene, which encodes sarcoplasmic/endoplasmic reticulum calcium–ATPase type 2 (SERCA2). There is no validated scoring system for DD to enable proper RCTs. An increased risk of cardiac failure has been demonstrated by a case-control study related to the role of this enzyme in the cardiac muscle.
General measures include antiseptic washes, liquid soap-free washes, and loose, cotton clothing. Some patients flare with ultraviolet (UV) exposure and need photoprotection.
In mild disease or linear disease reflecting genetic mosaicism, topical retinoids may be sufficient. These include topical isotretinoin (0.05%), tretinoin cream (0.05%), adapalene gel (0.1%), and tazarotene gel (0.1% short contact for 15 minutes). Treatment is applied on alternate days to begin with, increasing to once daily if possible, as irritation is common. The addition of a topical corticosteroid (alternating with the retinoid) may alleviate some of the side effects. Superinfection with viruses and bacteria is frequent, so combined corticosteroid/antibiotic preparations are logical. Sweating may be reduced by a trial of oral naltrexone.
In more extensive disease, an oral retinoid is required. Isotretinoin (0.5–1.0 mg/kg daily) and alitretinoin (30 mg daily) are preferred over acitretin because teratogenicity is a problem, and pregnancy is contraindicated for 2 years after stopping treatment with acitretin and 1 month after isotretinoin or alitretinoin. In males acitretin is an alternative but, bearing in mind that 50% of genetic relatives may have the same condition, such drugs could be dangerous if shared among females in the family. Compliance with contraceptive measures in females is very important as the treatment is usually long term.
The rare vesiculobullous form of the disease may respond to prednisolone. Hypertrophic flexural disease unresponsive to retinoids may require a surgical approach with laser , electrosurgery , debridement , or excision . Recurrence is a problem.
Oral lithium exacerbates the disease and should be avoided if possible.
Burge SM, Wilkinson JD. J Am Acad Dermatol 1992; 27: 40–50.
Fourteen percent of patients in this series had herpes simplex complicating their disease.
Painful blisters arising in a patient with DD are usually due to secondary infection with Staphylococcus aureus or herpes simplex.
Cooper SM, Burge SM. Am J Clin Dermatol 2003; 4: 97–105.
A detailed review of the management of DD.
Genetic counseling can be helpful, and written information is often appreciated.
Burge SM, Buxton PK. Br J Dermatol 1995; 133: 924–8.
Six of 11 patients improved with 0.05% isotretinoin gel applied to a test patch. Patients were treated up to twice/day for 3 months if tolerated. Erythema, burning, and irritation were common. All patients relapsed after 1 month of stopping the treatment.
Abe M, Inoue C, Yokoyama Y, et al. Pediatr Dermatol 2011; 28: 197–8.
Adapalene gel 0.1% applied daily for 2 months to the right side of the abdomen of a 12-year-old boy resulted in dramatic improvement in the area that was treated.
C G Burkhart CG, Burkhart CN. J Am Acad Dermatol 1998; 38: 1001–2.
Sanz-Sánchez T, Díaz-Díaz RM, López-Barrantes O, et al. Actas Dermosifiliogr 2012; 103: 255–6.
Tazarotene has been used effectively as short contact or with topical steroids with improvement within 3 months.
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