Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology

Background: Within the last decade, confocal microscopy has become a valuable non-invasive diagnostic tool in imaging human skin in vivo. Of the two different methods that exist, reflectance confocal microscopy (RCM) displays the backscattering signal of naturally occurring skin components, whereas...

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Autores principales: Hans Skvara, Ulrike Plut, Johannes A. Schmid, Constanze Jonak
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Lenguaje:EN
Publicado: Mattioli1885 2012
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Acceso en línea:https://doaj.org/article/ed5bde5a7ede4a6bb8cd0c71f9026779
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spelling oai:doaj.org-article:ed5bde5a7ede4a6bb8cd0c71f90267792021-11-17T08:33:18ZCombining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology10.5826/dpc.0201a022160-9381https://doaj.org/article/ed5bde5a7ede4a6bb8cd0c71f90267792012-01-01T00:00:00Zhttp://dpcj.org/index.php/dpc/article/view/994https://doaj.org/toc/2160-9381 Background: Within the last decade, confocal microscopy has become a valuable non-invasive diagnostic tool in imaging human skin in vivo. Of the two different methods that exist, reflectance confocal microscopy (RCM) displays the backscattering signal of naturally occurring skin components, whereas fluorescence confocal microscopy (FCM) provides contrast by using an exogenously applied fluorescent dye. Methodology: A newly developed multilaser device, in which both techniques are implemented, has been used to combine both methods and allows to highlight different information in one image. In our study, we applied the fluorophore sodium fluorescein (SFL) intradermally on forearm skin of 10 healthy volunteers followed by fluorescence and reflectance imaging. Results: In fluorescence mode the intercellular distribution of SFL clearly outlines every single cell in the epidermis, whereas in reflectance mode keratin and melanin-rich cells and structures provide additional information. The combination of both methods enables a clear delineation between the cell border, the cytoplasm and the nucleus. Imaging immediately, 20, 40 and 60 minutes after SFL injection, represents the dynamic distribution pattern of the dye. Conclusion: The synergism of RCM and FCM in one device delivering accurate information on skin architecture and pigmentation will have a great impact on in vivo diagnosis of human skin in the future. Hans SkvaraUlrike PlutJohannes A. SchmidConstanze JonakMattioli1885articleconfocal microscopyfluorescencereflectancesodium fluoresceinin vivohealthy human skinDermatologyRL1-803ENDermatology Practical & Conceptual (2012)
institution DOAJ
collection DOAJ
language EN
topic confocal microscopy
fluorescence
reflectance
sodium fluorescein
in vivo
healthy human skin
Dermatology
RL1-803
spellingShingle confocal microscopy
fluorescence
reflectance
sodium fluorescein
in vivo
healthy human skin
Dermatology
RL1-803
Hans Skvara
Ulrike Plut
Johannes A. Schmid
Constanze Jonak
Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
description Background: Within the last decade, confocal microscopy has become a valuable non-invasive diagnostic tool in imaging human skin in vivo. Of the two different methods that exist, reflectance confocal microscopy (RCM) displays the backscattering signal of naturally occurring skin components, whereas fluorescence confocal microscopy (FCM) provides contrast by using an exogenously applied fluorescent dye. Methodology: A newly developed multilaser device, in which both techniques are implemented, has been used to combine both methods and allows to highlight different information in one image. In our study, we applied the fluorophore sodium fluorescein (SFL) intradermally on forearm skin of 10 healthy volunteers followed by fluorescence and reflectance imaging. Results: In fluorescence mode the intercellular distribution of SFL clearly outlines every single cell in the epidermis, whereas in reflectance mode keratin and melanin-rich cells and structures provide additional information. The combination of both methods enables a clear delineation between the cell border, the cytoplasm and the nucleus. Imaging immediately, 20, 40 and 60 minutes after SFL injection, represents the dynamic distribution pattern of the dye. Conclusion: The synergism of RCM and FCM in one device delivering accurate information on skin architecture and pigmentation will have a great impact on in vivo diagnosis of human skin in the future.
format article
author Hans Skvara
Ulrike Plut
Johannes A. Schmid
Constanze Jonak
author_facet Hans Skvara
Ulrike Plut
Johannes A. Schmid
Constanze Jonak
author_sort Hans Skvara
title Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
title_short Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
title_full Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
title_fullStr Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
title_full_unstemmed Combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
title_sort combining in vivo reflectance with fluorescence confocal microscopy provides additive information on skin morphology
publisher Mattioli1885
publishDate 2012
url https://doaj.org/article/ed5bde5a7ede4a6bb8cd0c71f9026779
work_keys_str_mv AT hansskvara combininginvivoreflectancewithfluorescenceconfocalmicroscopyprovidesadditiveinformationonskinmorphology
AT ulrikeplut combininginvivoreflectancewithfluorescenceconfocalmicroscopyprovidesadditiveinformationonskinmorphology
AT johannesaschmid combininginvivoreflectancewithfluorescenceconfocalmicroscopyprovidesadditiveinformationonskinmorphology
AT constanzejonak combininginvivoreflectancewithfluorescenceconfocalmicroscopyprovidesadditiveinformationonskinmorphology
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