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A pilot study using reflectance confocal microscopy (RCM) in the assessment of a novel formulation for the treatment of melasma.
DC Field | Value | Language |
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dc.contributor.author | Tsilika, K | - |
dc.contributor.author | Levy, JL | - |
dc.contributor.author | Kang, HY | - |
dc.contributor.author | Duteil, L | - |
dc.contributor.author | Khemis, A | - |
dc.contributor.author | Hughes, R | - |
dc.contributor.author | Passeron, T | - |
dc.contributor.author | Ortonne, JP | - |
dc.contributor.author | Bahadoran, P | - |
dc.date.accessioned | 2012-05-09T01:24:48Z | - |
dc.date.available | 2012-05-09T01:24:48Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 1545-9616 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/6868 | - |
dc.description.abstract | INTRODUCTION: Melasma is a common pigmentary disorder caused by abnormal melanin deposits within the skin. Hydroquinone (HQ) is presently the most popular depigmenting agent, however the treatment of melasma remains unsatisfactory, resulting in a need to evaluate new depigmenting agents.
OBJECTIVE: The objective of this study was to assess, using standard methods and a novel technique, in vivo Reflectance Confocal Microscopy (RCM), the efficacy and safety of a new non-HQ bleaching agent Dermamelan® (Mesoestetic, Barcelona, Spain) in the treatment of melasma. METHODS: Ten women with melasma were enrolled in an open-label trial lasting four months. Patients were of Fitzpatrick skin types II-IV. A non-HQ depigmenting agent (Dermamelan) was applied once-daily for three months. Melasma Area and Severity Indices (MASI) were measured. Standard and UV-light photographs were taken and in vivo RCM, which detects pigmentary changes at a cellular level, was done. Evaluations were performed before treatment, on the first, second and third month of treatment and one month after treatment. Upon cessation of the trial, patients completed a questionnaire regarding efficacy and tolerance. RESULTS: At baseline, RCM detected hyperpigmented keratinocytes in all patients, dendritic cells in 2/10 patients, and melanophages in 2/10 patients. Based on the MASI score, Dermamelan treatment improved melasma by 50 percent. This was confirmed by standard and UV-light photography. Maximum therapeutic effect was usually reached by one month of treatment and was maintained at one month following its completion. Interestingly Dermamelan treatment also induced a statistically significant decrease of pigmented epidermal keratinocytes as detected by RCM. Patients with melanophages on RCM at baseline had a poorer outcome, but not those with dendritic cells. Mild irritation was the only adverse event observed during treatment. The majority of patients were satisfied with the result. CONCLUSION: This study suggests that Dermamelan produces significant rapid improvement of melasma at a clinical and cellular level and demonstrates the potential of RCM to monitor and possibly predict efficacy of a new depigmenting agent in the treatment of melasma. | - |
dc.language.iso | en | - |
dc.subject.MESH | Dendritic Cells | - |
dc.subject.MESH | Dermatologic Agents | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Follow-Up Studies | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Keratinocytes | - |
dc.subject.MESH | Melanosis | - |
dc.subject.MESH | Microscopy, Confocal | - |
dc.subject.MESH | Patient Satisfaction | - |
dc.subject.MESH | Pilot Projects | - |
dc.subject.MESH | Questionnaires | - |
dc.subject.MESH | Severity of Illness Index | - |
dc.subject.MESH | Treatment Outcome | - |
dc.title | A pilot study using reflectance confocal microscopy (RCM) in the assessment of a novel formulation for the treatment of melasma. | - |
dc.type | Article | - |
dc.identifier.pmid | 22052305 | - |
dc.contributor.affiliatedAuthor | 강, 희영 | - |
dc.type.local | Journal Papers | - |
dc.citation.title | Journal of drugs in dermatology : JDD | - |
dc.citation.volume | 10 | - |
dc.citation.number | 11 | - |
dc.citation.date | 2011 | - |
dc.citation.startPage | 1260 | - |
dc.citation.endPage | 1264 | - |
dc.identifier.bibliographicCitation | Journal of drugs in dermatology : JDD, 10(11). : 1260-1264, 2011 | - |
dc.relation.journalid | J015459616 | - |
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