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In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas
BACKGROUND: Human cutaneous malignant melanoma (CMM) is an aggressive cancer showing a dramatic worldwide increase in incidence over the past few decades. The most prominent relative epidemiological increase has been disclosed in young women. The aim of the study was to assess the effects of chronic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149332/ https://www.ncbi.nlm.nih.gov/pubmed/25187731 http://dx.doi.org/10.2147/CCID.S66929 |
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author | Piérard, Gérald E Hermanns-Lê, Trinh Piérard, Sébastien L Dewalque, Lucas Charlier, Corinne Piérard-Franchimont, Claudine Delvenne, Philippe |
author_facet | Piérard, Gérald E Hermanns-Lê, Trinh Piérard, Sébastien L Dewalque, Lucas Charlier, Corinne Piérard-Franchimont, Claudine Delvenne, Philippe |
author_sort | Piérard, Gérald E |
collection | PubMed |
description | BACKGROUND: Human cutaneous malignant melanoma (CMM) is an aggressive cancer showing a dramatic worldwide increase in incidence over the past few decades. The most prominent relative epidemiological increase has been disclosed in young women. The aim of the study was to assess the effects of chronic sun exposures in order to rate the extend of melanocytic stimulations in the vicinity of CMM. METHODS: The study was designed to evaluate the melanin distribution and density using ultraviolet light illumination. The present study was performed on surgical excision specimens of thin CMM lesion removed from the upper limbs of 55 Caucasian adults (37 women and 18 men). Two control groups comprised 23 men and 21 women of similar ages who had medium-size congenital melanocytic nevi, also present on the upper limbs. The peritumoral skin was scrutinized using a Visioscan(®) VC98 device, revealing the faint mosaic melanoderma (FMM) pattern that grossly indicates early signs of chronic photodamage in epidermal melanin units. RESULTS: The median extent of relative FMM was significantly higher in the CMM male group. By contrast, the CMM female group showed a reverse bimodal distribution in FMM size. Only 12/37 (32.5%) of the CMM female group had an increased FMM size, whereas 25/37 (67.5%) of females with CMM had a global FMM extent in the normal range, relative to the controls. CONCLUSION: Thin CMM supervening in young women appear unrelated to repeat photoexposure. Other mechanisms are possibly involved. |
format | Online Article Text |
id | pubmed-4149332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41493322014-09-03 In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas Piérard, Gérald E Hermanns-Lê, Trinh Piérard, Sébastien L Dewalque, Lucas Charlier, Corinne Piérard-Franchimont, Claudine Delvenne, Philippe Clin Cosmet Investig Dermatol Original Research BACKGROUND: Human cutaneous malignant melanoma (CMM) is an aggressive cancer showing a dramatic worldwide increase in incidence over the past few decades. The most prominent relative epidemiological increase has been disclosed in young women. The aim of the study was to assess the effects of chronic sun exposures in order to rate the extend of melanocytic stimulations in the vicinity of CMM. METHODS: The study was designed to evaluate the melanin distribution and density using ultraviolet light illumination. The present study was performed on surgical excision specimens of thin CMM lesion removed from the upper limbs of 55 Caucasian adults (37 women and 18 men). Two control groups comprised 23 men and 21 women of similar ages who had medium-size congenital melanocytic nevi, also present on the upper limbs. The peritumoral skin was scrutinized using a Visioscan(®) VC98 device, revealing the faint mosaic melanoderma (FMM) pattern that grossly indicates early signs of chronic photodamage in epidermal melanin units. RESULTS: The median extent of relative FMM was significantly higher in the CMM male group. By contrast, the CMM female group showed a reverse bimodal distribution in FMM size. Only 12/37 (32.5%) of the CMM female group had an increased FMM size, whereas 25/37 (67.5%) of females with CMM had a global FMM extent in the normal range, relative to the controls. CONCLUSION: Thin CMM supervening in young women appear unrelated to repeat photoexposure. Other mechanisms are possibly involved. Dove Medical Press 2014-08-22 /pmc/articles/PMC4149332/ /pubmed/25187731 http://dx.doi.org/10.2147/CCID.S66929 Text en © 2014 Piérard et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Piérard, Gérald E Hermanns-Lê, Trinh Piérard, Sébastien L Dewalque, Lucas Charlier, Corinne Piérard-Franchimont, Claudine Delvenne, Philippe In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title | In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title_full | In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title_fullStr | In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title_full_unstemmed | In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title_short | In vivo skin fluorescence imaging in young Caucasian adults with early malignant melanomas |
title_sort | in vivo skin fluorescence imaging in young caucasian adults with early malignant melanomas |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149332/ https://www.ncbi.nlm.nih.gov/pubmed/25187731 http://dx.doi.org/10.2147/CCID.S66929 |
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