The clinical efficacy and tolerability of the topical receptor-selective
retinoid tazarotene in the treatment of congenital
ichthyoses was investigated. Twelve consecutive patients with different forms of congenital
ichthyosis were enrolled in an open, non-randomized, intraindividually controlled, half-side pilot study. Diagnoses were X-linked recessive
ichthyosis, non-erythrodermic autosomal recessive
lamellar ichthyosis, autosomal dominant ichthyosis vulgaris and
ichthyosis bullosa of Siemens (IBS).
Tazarotene 0.05% gel was applied unilaterally daily on a defined body area measuring 10% of the body surface area. The contralateral side was treated with an
ointment containing 10%
urea. After 14 days, application frequency was reduced to three times a week, and stopped after another 2 weeks. The follow-up period was 3 months. Reduction in scaling and roughness was used to assess the clinical response in the
tazarotene-treated area compared with the control area. Clinical and laboratory assessments were performed every 14 days during the trial. Unilateral improvement in favour of the
tazarotene-treated side was observed in nine of 12 patients (75%). Four patients (33%) achieved an excellent response and four (33%) achieved a good response. No
therapeutic effect was seen in patients with IBS. The remission persisted during the reduction phase and after discontinuation for up to 2 months. Local irritation in three patients was the only side-effect detectable. Short-term topical application of
tazarotene 0.05% gel is a very effective and well-tolerated treatment modality in different forms of congenital
ichthyoses and may be an alternative to systemic
retinoid therapy.