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Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo
Melanoma is associated with angiogenesis and vascular changes that may extend through the entire skin depth. Three-dimensional imaging of vascular characteristics in skin lesions could therefore allow diagnostic insights not available by conventional visual inspection. Raster-scan optoacoustic mesos...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120110/ https://www.ncbi.nlm.nih.gov/pubmed/35589757 http://dx.doi.org/10.1038/s41467-022-30471-9 |
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author | He, Hailong Schönmann, Christine Schwarz, Mathias Hindelang, Benedikt Berezhnoi, Andrei Steimle-Grauer, Susanne Annette Darsow, Ulf Aguirre, Juan Ntziachristos, Vasilis |
author_facet | He, Hailong Schönmann, Christine Schwarz, Mathias Hindelang, Benedikt Berezhnoi, Andrei Steimle-Grauer, Susanne Annette Darsow, Ulf Aguirre, Juan Ntziachristos, Vasilis |
author_sort | He, Hailong |
collection | PubMed |
description | Melanoma is associated with angiogenesis and vascular changes that may extend through the entire skin depth. Three-dimensional imaging of vascular characteristics in skin lesions could therefore allow diagnostic insights not available by conventional visual inspection. Raster-scan optoacoustic mesoscopy (RSOM) images microvasculature through the entire skin depth with resolutions of tens of micrometers; however, current RSOM implementations are too slow to overcome the strong breathing motions on the upper torso where melanoma lesions commonly occur. To enable high-resolution imaging of melanoma vasculature in humans, we accelerate RSOM scanning using an illumination scheme that is coaxial with a high-sensitivity ultrasound detector path, yielding 15 s single-breath-hold scans that minimize motion artifacts. We apply this Fast RSOM to image 10 melanomas and 10 benign nevi in vivo, showing marked differences between malignant and benign lesions, supporting the possibility to use biomarkers extracted from RSOM imaging of vasculature for lesion characterization to improve diagnostics. |
format | Online Article Text |
id | pubmed-9120110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91201102022-05-21 Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo He, Hailong Schönmann, Christine Schwarz, Mathias Hindelang, Benedikt Berezhnoi, Andrei Steimle-Grauer, Susanne Annette Darsow, Ulf Aguirre, Juan Ntziachristos, Vasilis Nat Commun Article Melanoma is associated with angiogenesis and vascular changes that may extend through the entire skin depth. Three-dimensional imaging of vascular characteristics in skin lesions could therefore allow diagnostic insights not available by conventional visual inspection. Raster-scan optoacoustic mesoscopy (RSOM) images microvasculature through the entire skin depth with resolutions of tens of micrometers; however, current RSOM implementations are too slow to overcome the strong breathing motions on the upper torso where melanoma lesions commonly occur. To enable high-resolution imaging of melanoma vasculature in humans, we accelerate RSOM scanning using an illumination scheme that is coaxial with a high-sensitivity ultrasound detector path, yielding 15 s single-breath-hold scans that minimize motion artifacts. We apply this Fast RSOM to image 10 melanomas and 10 benign nevi in vivo, showing marked differences between malignant and benign lesions, supporting the possibility to use biomarkers extracted from RSOM imaging of vasculature for lesion characterization to improve diagnostics. Nature Publishing Group UK 2022-05-19 /pmc/articles/PMC9120110/ /pubmed/35589757 http://dx.doi.org/10.1038/s41467-022-30471-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Hailong Schönmann, Christine Schwarz, Mathias Hindelang, Benedikt Berezhnoi, Andrei Steimle-Grauer, Susanne Annette Darsow, Ulf Aguirre, Juan Ntziachristos, Vasilis Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title | Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title_full | Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title_fullStr | Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title_full_unstemmed | Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title_short | Fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
title_sort | fast raster-scan optoacoustic mesoscopy enables assessment of human melanoma microvasculature in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120110/ https://www.ncbi.nlm.nih.gov/pubmed/35589757 http://dx.doi.org/10.1038/s41467-022-30471-9 |
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