Loading…

In vivo multiphoton microscopy imaging of melasma

Melasma is a skin disorder characterized by hyperpigmented patches due to increased melanin production and deposition. In this pilot study we evaluate the potential of multiphoton microscopy (MPM) to characterize non-invasively the melanin content, location, and distribution in melasma and assess th...

Full description

Saved in:
Bibliographic Details
Published in:Pigment cell and melanoma research 2018-12, Vol.32 (3), p.403-411
Main Authors: Lentsch, Griffin, Balu, Mihaela, Williams, Joshua, Lee, Sanghoon, Harris, Ronald M., König, Karsten, Ganesan, Anand, Tromberg, Bruce J., Nair, Nirmala, Santhanam, Uma, Misra, Manoj
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 411
container_issue 3
container_start_page 403
container_title Pigment cell and melanoma research
container_volume 32
creator Lentsch, Griffin
Balu, Mihaela
Williams, Joshua
Lee, Sanghoon
Harris, Ronald M.
König, Karsten
Ganesan, Anand
Tromberg, Bruce J.
Nair, Nirmala
Santhanam, Uma
Misra, Manoj
description Melasma is a skin disorder characterized by hyperpigmented patches due to increased melanin production and deposition. In this pilot study we evaluate the potential of multiphoton microscopy (MPM) to characterize non-invasively the melanin content, location, and distribution in melasma and assess the elastosis severity. We employed a clinical MPM tomograph to image in-vivo morphological features in melasma lesions and adjacent normal skin in 12 patients. We imaged dermal melanophages in most dermal melasma lesions and occasionally in epidermal melasma. The melanin volume fraction values measured in epidermal melasma (14±4%) were significantly higher (p
doi_str_mv 10.1111/pcmr.12756
format article
fullrecord <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6483848</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_6483848</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_64838483</originalsourceid><addsrcrecordid>eNqljL0KwjAAhIMo1r_FJ8gLtCZtk9bFRRTdHdxCjP2JND8kbaFvbwcRnD047oPjDoAtRhEetbNCuQjHGaETsMAZISFO8_v0yxkOwNL7F0IUkX0yB0GCCKI0zhYAXzXsZW-g6ppW2tq0RkMlhTNeGDtAqXgldQVNCVXRcK_4GsxK3vhi88kVOJxPt-MltN1DFU9R6Nbxhlk3Tt3ADJfst9GyZpXpGU3zJB_998Ebk3BSxQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>In vivo multiphoton microscopy imaging of melasma</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Lentsch, Griffin ; Balu, Mihaela ; Williams, Joshua ; Lee, Sanghoon ; Harris, Ronald M. ; König, Karsten ; Ganesan, Anand ; Tromberg, Bruce J. ; Nair, Nirmala ; Santhanam, Uma ; Misra, Manoj</creator><creatorcontrib>Lentsch, Griffin ; Balu, Mihaela ; Williams, Joshua ; Lee, Sanghoon ; Harris, Ronald M. ; König, Karsten ; Ganesan, Anand ; Tromberg, Bruce J. ; Nair, Nirmala ; Santhanam, Uma ; Misra, Manoj</creatorcontrib><description>Melasma is a skin disorder characterized by hyperpigmented patches due to increased melanin production and deposition. In this pilot study we evaluate the potential of multiphoton microscopy (MPM) to characterize non-invasively the melanin content, location, and distribution in melasma and assess the elastosis severity. We employed a clinical MPM tomograph to image in-vivo morphological features in melasma lesions and adjacent normal skin in 12 patients. We imaged dermal melanophages in most dermal melasma lesions and occasionally in epidermal melasma. The melanin volume fraction values measured in epidermal melasma (14±4%) were significantly higher (p&lt;0.05) than the values measured in peri-lesional skin (11±3%). The basal keratinocytes of melasma and perilesions showed different melanin distribution. Elastosis was predominantly more severe in lesions than in perilesions and was associated with changes in melanin distribution of the basal keratinocytes. These results demonstrate that MPM may be a non-invasive imaging tool for characterizing melasma.</description><identifier>ISSN: 1755-1471</identifier><identifier>EISSN: 1755-148X</identifier><identifier>DOI: 10.1111/pcmr.12756</identifier><identifier>PMID: 30506627</identifier><language>eng</language><ispartof>Pigment cell and melanoma research, 2018-12, Vol.32 (3), p.403-411</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids></links><search><creatorcontrib>Lentsch, Griffin</creatorcontrib><creatorcontrib>Balu, Mihaela</creatorcontrib><creatorcontrib>Williams, Joshua</creatorcontrib><creatorcontrib>Lee, Sanghoon</creatorcontrib><creatorcontrib>Harris, Ronald M.</creatorcontrib><creatorcontrib>König, Karsten</creatorcontrib><creatorcontrib>Ganesan, Anand</creatorcontrib><creatorcontrib>Tromberg, Bruce J.</creatorcontrib><creatorcontrib>Nair, Nirmala</creatorcontrib><creatorcontrib>Santhanam, Uma</creatorcontrib><creatorcontrib>Misra, Manoj</creatorcontrib><title>In vivo multiphoton microscopy imaging of melasma</title><title>Pigment cell and melanoma research</title><description>Melasma is a skin disorder characterized by hyperpigmented patches due to increased melanin production and deposition. In this pilot study we evaluate the potential of multiphoton microscopy (MPM) to characterize non-invasively the melanin content, location, and distribution in melasma and assess the elastosis severity. We employed a clinical MPM tomograph to image in-vivo morphological features in melasma lesions and adjacent normal skin in 12 patients. We imaged dermal melanophages in most dermal melasma lesions and occasionally in epidermal melasma. The melanin volume fraction values measured in epidermal melasma (14±4%) were significantly higher (p&lt;0.05) than the values measured in peri-lesional skin (11±3%). The basal keratinocytes of melasma and perilesions showed different melanin distribution. Elastosis was predominantly more severe in lesions than in perilesions and was associated with changes in melanin distribution of the basal keratinocytes. These results demonstrate that MPM may be a non-invasive imaging tool for characterizing melasma.</description><issn>1755-1471</issn><issn>1755-148X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqljL0KwjAAhIMo1r_FJ8gLtCZtk9bFRRTdHdxCjP2JND8kbaFvbwcRnD047oPjDoAtRhEetbNCuQjHGaETsMAZISFO8_v0yxkOwNL7F0IUkX0yB0GCCKI0zhYAXzXsZW-g6ppW2tq0RkMlhTNeGDtAqXgldQVNCVXRcK_4GsxK3vhi88kVOJxPt-MltN1DFU9R6Nbxhlk3Tt3ADJfst9GyZpXpGU3zJB_998Ebk3BSxQ</recordid><startdate>20181221</startdate><enddate>20181221</enddate><creator>Lentsch, Griffin</creator><creator>Balu, Mihaela</creator><creator>Williams, Joshua</creator><creator>Lee, Sanghoon</creator><creator>Harris, Ronald M.</creator><creator>König, Karsten</creator><creator>Ganesan, Anand</creator><creator>Tromberg, Bruce J.</creator><creator>Nair, Nirmala</creator><creator>Santhanam, Uma</creator><creator>Misra, Manoj</creator><scope>5PM</scope></search><sort><creationdate>20181221</creationdate><title>In vivo multiphoton microscopy imaging of melasma</title><author>Lentsch, Griffin ; Balu, Mihaela ; Williams, Joshua ; Lee, Sanghoon ; Harris, Ronald M. ; König, Karsten ; Ganesan, Anand ; Tromberg, Bruce J. ; Nair, Nirmala ; Santhanam, Uma ; Misra, Manoj</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_64838483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lentsch, Griffin</creatorcontrib><creatorcontrib>Balu, Mihaela</creatorcontrib><creatorcontrib>Williams, Joshua</creatorcontrib><creatorcontrib>Lee, Sanghoon</creatorcontrib><creatorcontrib>Harris, Ronald M.</creatorcontrib><creatorcontrib>König, Karsten</creatorcontrib><creatorcontrib>Ganesan, Anand</creatorcontrib><creatorcontrib>Tromberg, Bruce J.</creatorcontrib><creatorcontrib>Nair, Nirmala</creatorcontrib><creatorcontrib>Santhanam, Uma</creatorcontrib><creatorcontrib>Misra, Manoj</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pigment cell and melanoma research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lentsch, Griffin</au><au>Balu, Mihaela</au><au>Williams, Joshua</au><au>Lee, Sanghoon</au><au>Harris, Ronald M.</au><au>König, Karsten</au><au>Ganesan, Anand</au><au>Tromberg, Bruce J.</au><au>Nair, Nirmala</au><au>Santhanam, Uma</au><au>Misra, Manoj</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo multiphoton microscopy imaging of melasma</atitle><jtitle>Pigment cell and melanoma research</jtitle><date>2018-12-21</date><risdate>2018</risdate><volume>32</volume><issue>3</issue><spage>403</spage><epage>411</epage><pages>403-411</pages><issn>1755-1471</issn><eissn>1755-148X</eissn><abstract>Melasma is a skin disorder characterized by hyperpigmented patches due to increased melanin production and deposition. In this pilot study we evaluate the potential of multiphoton microscopy (MPM) to characterize non-invasively the melanin content, location, and distribution in melasma and assess the elastosis severity. We employed a clinical MPM tomograph to image in-vivo morphological features in melasma lesions and adjacent normal skin in 12 patients. We imaged dermal melanophages in most dermal melasma lesions and occasionally in epidermal melasma. The melanin volume fraction values measured in epidermal melasma (14±4%) were significantly higher (p&lt;0.05) than the values measured in peri-lesional skin (11±3%). The basal keratinocytes of melasma and perilesions showed different melanin distribution. Elastosis was predominantly more severe in lesions than in perilesions and was associated with changes in melanin distribution of the basal keratinocytes. These results demonstrate that MPM may be a non-invasive imaging tool for characterizing melasma.</abstract><pmid>30506627</pmid><doi>10.1111/pcmr.12756</doi></addata></record>
fulltext fulltext
identifier ISSN: 1755-1471
ispartof Pigment cell and melanoma research, 2018-12, Vol.32 (3), p.403-411
issn 1755-1471
1755-148X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6483848
source Wiley-Blackwell Read & Publish Collection
title In vivo multiphoton microscopy imaging of melasma
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T22%3A07%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=In%20vivo%20multiphoton%20microscopy%20imaging%20of%20melasma&rft.jtitle=Pigment%20cell%20and%20melanoma%20research&rft.au=Lentsch,%20Griffin&rft.date=2018-12-21&rft.volume=32&rft.issue=3&rft.spage=403&rft.epage=411&rft.pages=403-411&rft.issn=1755-1471&rft.eissn=1755-148X&rft_id=info:doi/10.1111/pcmr.12756&rft_dat=%3Cpubmedcentral%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_6483848%3C/pubmedcentral%3E%3Cgrp_id%3Ecdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_64838483%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/30506627&rfr_iscdi=true