Cargando…
Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions
Malignant melanoma poses a clinical diagnostic problem, since a large number of benign lesions are excised to find a single melanoma. This study assessed the accuracy of a novel non-invasive diagnostic technology, hyperspectral imaging, for melanoma detection. Lesions were imaged prior to excision a...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Publication of Acta Dermato-Venereologica
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811300/ https://www.ncbi.nlm.nih.gov/pubmed/36281811 http://dx.doi.org/10.2340/actadv.v102.2045 |
_version_ | 1784863503621816320 |
---|---|
author | PAOLI, John PÖLÖNEN, Ilkka SALMIVUORI, Mari RÄSÄNEN, Janne ZAAR, Oscar POLESIE, Sam KOSKENMIES, Sari PITKÄNEN, Sari ÖVERMARK, Meri ISOHERRANEN, Kirsi JUTEAU, Susanna RANKI, Annamari GRÖNROOS, Mari NEITTAANMÄKI, Noora |
author_facet | PAOLI, John PÖLÖNEN, Ilkka SALMIVUORI, Mari RÄSÄNEN, Janne ZAAR, Oscar POLESIE, Sam KOSKENMIES, Sari PITKÄNEN, Sari ÖVERMARK, Meri ISOHERRANEN, Kirsi JUTEAU, Susanna RANKI, Annamari GRÖNROOS, Mari NEITTAANMÄKI, Noora |
author_sort | PAOLI, John |
collection | PubMed |
description | Malignant melanoma poses a clinical diagnostic problem, since a large number of benign lesions are excised to find a single melanoma. This study assessed the accuracy of a novel non-invasive diagnostic technology, hyperspectral imaging, for melanoma detection. Lesions were imaged prior to excision and histopathological analysis. A deep neural network algorithm was trained twice to distinguish between histopathologically verified malignant and benign melanocytic lesions and to classify the separate subgroups. Furthermore, 2 different approaches were used: a majority vote classification and a pixel-wise classification. The study included 325 lesions from 285 patients. Of these, 74 were invasive melanoma, 88 melanoma in situ, 115 dysplastic naevi, and 48 non-dysplastic naevi. The study included a training set of 358,800 pixels and a validation set of 7,313 pixels, which was then tested with a training set of 24,375 pixels. The majority vote classification achieved high overall sensitivity of 95% and a specificity of 92% (95% confidence interval (95% CI) 0.024–0.029) in differentiating malignant from benign lesions. In the pixel-wise classification, the overall sensitivity and specificity were both 82% (95% CI 0.005–0.005). When divided into 4 subgroups, the diagnostic accuracy was lower. Hyperspectral imaging provides high sensitivity and specificity in distinguishing between naevi and melanoma. This novel method still needs further validation. |
format | Online Article Text |
id | pubmed-9811300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Publication of Acta Dermato-Venereologica |
record_format | MEDLINE/PubMed |
spelling | pubmed-98113002023-02-08 Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions PAOLI, John PÖLÖNEN, Ilkka SALMIVUORI, Mari RÄSÄNEN, Janne ZAAR, Oscar POLESIE, Sam KOSKENMIES, Sari PITKÄNEN, Sari ÖVERMARK, Meri ISOHERRANEN, Kirsi JUTEAU, Susanna RANKI, Annamari GRÖNROOS, Mari NEITTAANMÄKI, Noora Acta Derm Venereol Original Article Malignant melanoma poses a clinical diagnostic problem, since a large number of benign lesions are excised to find a single melanoma. This study assessed the accuracy of a novel non-invasive diagnostic technology, hyperspectral imaging, for melanoma detection. Lesions were imaged prior to excision and histopathological analysis. A deep neural network algorithm was trained twice to distinguish between histopathologically verified malignant and benign melanocytic lesions and to classify the separate subgroups. Furthermore, 2 different approaches were used: a majority vote classification and a pixel-wise classification. The study included 325 lesions from 285 patients. Of these, 74 were invasive melanoma, 88 melanoma in situ, 115 dysplastic naevi, and 48 non-dysplastic naevi. The study included a training set of 358,800 pixels and a validation set of 7,313 pixels, which was then tested with a training set of 24,375 pixels. The majority vote classification achieved high overall sensitivity of 95% and a specificity of 92% (95% confidence interval (95% CI) 0.024–0.029) in differentiating malignant from benign lesions. In the pixel-wise classification, the overall sensitivity and specificity were both 82% (95% CI 0.005–0.005). When divided into 4 subgroups, the diagnostic accuracy was lower. Hyperspectral imaging provides high sensitivity and specificity in distinguishing between naevi and melanoma. This novel method still needs further validation. Society for Publication of Acta Dermato-Venereologica 2022-11-14 /pmc/articles/PMC9811300/ /pubmed/36281811 http://dx.doi.org/10.2340/actadv.v102.2045 Text en © 2022 Acta Dermato-Venereologica https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license |
spellingShingle | Original Article PAOLI, John PÖLÖNEN, Ilkka SALMIVUORI, Mari RÄSÄNEN, Janne ZAAR, Oscar POLESIE, Sam KOSKENMIES, Sari PITKÄNEN, Sari ÖVERMARK, Meri ISOHERRANEN, Kirsi JUTEAU, Susanna RANKI, Annamari GRÖNROOS, Mari NEITTAANMÄKI, Noora Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title | Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title_full | Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title_fullStr | Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title_full_unstemmed | Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title_short | Hyperspectral Imaging for Non-invasive Diagnostics of Melanocytic Lesions |
title_sort | hyperspectral imaging for non-invasive diagnostics of melanocytic lesions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811300/ https://www.ncbi.nlm.nih.gov/pubmed/36281811 http://dx.doi.org/10.2340/actadv.v102.2045 |
work_keys_str_mv | AT paolijohn hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT polonenilkka hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT salmivuorimari hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT rasanenjanne hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT zaaroscar hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT polesiesam hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT koskenmiessari hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT pitkanensari hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT overmarkmeri hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT isoherranenkirsi hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT juteaususanna hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT rankiannamari hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT gronroosmari hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions AT neittaanmakinoora hyperspectralimagingfornoninvasivediagnosticsofmelanocyticlesions |