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Hyperspectral imaging for tumor segmentation on pigmented skin lesions
SIGNIFICANCE: Malignant skin tumors, which include melanoma and nonmelanoma skin cancers, are the most prevalent type of malignant tumor. Gross pathology of pigmented skin lesions (PSL) remains manual, time-consuming, and heavily dependent on the expertise of the medical personnel. Hyperspectral ima...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619132/ https://www.ncbi.nlm.nih.gov/pubmed/36316301 http://dx.doi.org/10.1117/1.JBO.27.10.106007 |
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author | Aloupogianni, Eleni Ichimura, Takaya Hamada, Mei Ishikawa, Masahiro Murakami, Takuo Sasaki, Atsushi Nakamura, Koichiro Kobayashi, Naoki Obi, Takashi |
author_facet | Aloupogianni, Eleni Ichimura, Takaya Hamada, Mei Ishikawa, Masahiro Murakami, Takuo Sasaki, Atsushi Nakamura, Koichiro Kobayashi, Naoki Obi, Takashi |
author_sort | Aloupogianni, Eleni |
collection | PubMed |
description | SIGNIFICANCE: Malignant skin tumors, which include melanoma and nonmelanoma skin cancers, are the most prevalent type of malignant tumor. Gross pathology of pigmented skin lesions (PSL) remains manual, time-consuming, and heavily dependent on the expertise of the medical personnel. Hyperspectral imaging (HSI) can assist in the detection of tumors and evaluate the status of tumor margins by their spectral signatures. AIM: Tumor segmentation of medical HSI data is a research field. The goal of this study is to propose a framework for HSI-based tumor segmentation of PSL. APPROACH: An HSI dataset of 28 PSL was prepared. Two frameworks for data preprocessing and tumor segmentation were proposed. Models based on machine learning and deep learning were used at the core of each framework. RESULTS: Cross-validation performance showed that pixel-wise processing achieves higher segmentation performance, in terms of the Jaccard coefficient. Simultaneous use of spatio-spectral features produced more comprehensive tumor masks. A three-dimensional Xception-based network achieved performance similar to state-of-the-art networks while allowing for more detailed detection of the tumor border. CONCLUSIONS: Good performance was achieved for melanocytic lesions, but margins were difficult to detect in some cases of basal cell carcinoma. The frameworks proposed in this study could be further improved for robustness against different pathologies and detailed delineation of tissue margins to facilitate computer-assisted diagnosis during gross pathology. |
format | Online Article Text |
id | pubmed-9619132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-96191322022-11-01 Hyperspectral imaging for tumor segmentation on pigmented skin lesions Aloupogianni, Eleni Ichimura, Takaya Hamada, Mei Ishikawa, Masahiro Murakami, Takuo Sasaki, Atsushi Nakamura, Koichiro Kobayashi, Naoki Obi, Takashi J Biomed Opt Imaging SIGNIFICANCE: Malignant skin tumors, which include melanoma and nonmelanoma skin cancers, are the most prevalent type of malignant tumor. Gross pathology of pigmented skin lesions (PSL) remains manual, time-consuming, and heavily dependent on the expertise of the medical personnel. Hyperspectral imaging (HSI) can assist in the detection of tumors and evaluate the status of tumor margins by their spectral signatures. AIM: Tumor segmentation of medical HSI data is a research field. The goal of this study is to propose a framework for HSI-based tumor segmentation of PSL. APPROACH: An HSI dataset of 28 PSL was prepared. Two frameworks for data preprocessing and tumor segmentation were proposed. Models based on machine learning and deep learning were used at the core of each framework. RESULTS: Cross-validation performance showed that pixel-wise processing achieves higher segmentation performance, in terms of the Jaccard coefficient. Simultaneous use of spatio-spectral features produced more comprehensive tumor masks. A three-dimensional Xception-based network achieved performance similar to state-of-the-art networks while allowing for more detailed detection of the tumor border. CONCLUSIONS: Good performance was achieved for melanocytic lesions, but margins were difficult to detect in some cases of basal cell carcinoma. The frameworks proposed in this study could be further improved for robustness against different pathologies and detailed delineation of tissue margins to facilitate computer-assisted diagnosis during gross pathology. Society of Photo-Optical Instrumentation Engineers 2022-10-31 2022-10 /pmc/articles/PMC9619132/ /pubmed/36316301 http://dx.doi.org/10.1117/1.JBO.27.10.106007 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Imaging Aloupogianni, Eleni Ichimura, Takaya Hamada, Mei Ishikawa, Masahiro Murakami, Takuo Sasaki, Atsushi Nakamura, Koichiro Kobayashi, Naoki Obi, Takashi Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title | Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title_full | Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title_fullStr | Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title_full_unstemmed | Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title_short | Hyperspectral imaging for tumor segmentation on pigmented skin lesions |
title_sort | hyperspectral imaging for tumor segmentation on pigmented skin lesions |
topic | Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619132/ https://www.ncbi.nlm.nih.gov/pubmed/36316301 http://dx.doi.org/10.1117/1.JBO.27.10.106007 |
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