Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13773
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dc.contributor.authorTreesirichod A.
dc.contributor.authorChaithirayanon S.
dc.contributor.authorWongjitrat N.
dc.contributor.authorWattanapan P.
dc.date.accessioned2021-04-05T03:26:20Z-
dc.date.available2021-04-05T03:26:20Z-
dc.date.issued2015
dc.identifier.issn195154
dc.identifier.other2-s2.0-84920469459
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13773-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84920469459&doi=10.4103%2f0019-5154.147838&partnerID=40&md5=adf11149e729be85d4ca0e1ed09ab434
dc.description.abstractAims: To assess the degree of improvement of neck hyperpigmentation in childhood acanthosis nigricans (AN) after treatment with topical 0.1% adapalene gel and the assessment of localized tissue tolerance to the gel. Subjects and Methods: A split comparison study of the hyperpigmentation on the neck was conducted in patients diagnosed with childhood AN. Patients were treated with topical 0.1% adapalene gel for a period of 4 weeks. The skin color of their neck was evaluated at baseline, 2 weeks and 4 weeks using a skin color chart. Skin color ratio (the skin on their necks compared with the skin on their backs) was calculated for all subjects. The investigator's global evaluation (IGE) scale and the parent's global evaluation (PGE) scale were used to assess the efficacy of the patients' treatment at the end of the 4th week. Results: The mean skin color ratio of therapeutic side was significantly decreased from the baseline scores, at weeks 2 and 4, respectively (30.1%, 18.3%, and 12.9%, P < 0.001), with marked skin improvement at 60.7% ± 28.5%. The percentage of changes of skin color ratio was consistent with the efficacy evaluations as performed by the IGE and PGE scales. Treatment-related cutaneous irritation was minimal, predominantly in the first 2 weeks of treatment and was shown to be well-tolerated at week 4 following a modification of the treatment regimen. Conclusions: The study has shown the efficacy of topical 0.1% adapalene gel in the treatment of AN, specifically, in regards to the skin darkening with minimal cutaneous irritation. © 2015 Indian Journal of Dermatology.
dc.subjectadapalene
dc.subjectplacebo
dc.subjectacanthosis nigricans
dc.subjectadolescent
dc.subjectapplication site burning
dc.subjectapplication site dryness
dc.subjectapplication site erythema
dc.subjectapplication site irritation
dc.subjectapplication site pruritus
dc.subjectArticle
dc.subjectbody mass
dc.subjectchildhood disease
dc.subjectclinical article
dc.subjectclinical evaluation
dc.subjectcomparative effectiveness
dc.subjectcontrolled clinical trial
dc.subjectcontrolled study
dc.subjectdisease predisposition
dc.subjectdrug efficacy
dc.subjectdrug tolerability
dc.subjectdrug use
dc.subjectdry skin
dc.subjectfemale
dc.subjectgel
dc.subjecthuman
dc.subjecthyperpigmentation
dc.subjectmale
dc.subjectneck
dc.subjectobesity
dc.subjectpilot study
dc.subjectrating scale
dc.subjectskin abrasion
dc.subjectskin burning sensation
dc.subjectskin color
dc.subjectskin irritation
dc.subjectskin pruritus
dc.subjecttopical treatment
dc.subjecttreatment duration
dc.subjectweight change
dc.titleThe efficacy of topical 0.1% adapalene gel for use in the treatment of childhood acanthosis nigricans: A pilot study
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationIndian Journal of Dermatology. Vol 60, No.1 (2015), p.103-
dc.identifier.doi10.4103/0019-5154.147838
Appears in Collections:Scopus 1983-2021

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