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Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions

BACKGROUND: Diagnosis of oral cancer is conventionally carried out using white light endoscopy and histopathology of biopsy samples. However, oral tumours are mostly superficial and the lesion and its margins can be difficult to visualise under white light. We present clinical data on fluorescence d...

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Autores principales: Thong, P S P, Olivo, M, Chin, W W L, Bhuvaneswari, R, Mancer, K, Soo, K-C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778520/
https://www.ncbi.nlm.nih.gov/pubmed/19809432
http://dx.doi.org/10.1038/sj.bjc.6605357
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author Thong, P S P
Olivo, M
Chin, W W L
Bhuvaneswari, R
Mancer, K
Soo, K-C
author_facet Thong, P S P
Olivo, M
Chin, W W L
Bhuvaneswari, R
Mancer, K
Soo, K-C
author_sort Thong, P S P
collection PubMed
description BACKGROUND: Diagnosis of oral cancer is conventionally carried out using white light endoscopy and histopathology of biopsy samples. However, oral tumours are mostly superficial and the lesion and its margins can be difficult to visualise under white light. We present clinical data on fluorescence diagnostic imaging of oral lesions using hypericin, a plant-based photosensitiser. METHODS: Fluorescence images of lesions and normal tissue were captured using an endoscope after hypericin administration. The images were analysed to extract their colour parameters, which, along with the red-to-blue intensity ratios, were analysed and used to discriminate between tissue types. The results were correlated with those from histopathology. RESULTS: The red-to-blue intensity ratio increased from normal to hyperplastic to cancerous tissue and was a good parameter to discriminate between these tissue types, with sensitivity and specificity levels of 90% and above. CONCLUSION: Our results show that hypericin fluorescence imaging has the potential to be used for the clinical diagnosis of oral cancer. Further study to enhance the clinical potential of this technique includes the development of a real-time image processing and analysis system interfaced to the endoscope to enable same-day cancer diagnosis and demarcation of lesion margins in a clinical setting.
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spelling pubmed-27785202010-11-03 Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions Thong, P S P Olivo, M Chin, W W L Bhuvaneswari, R Mancer, K Soo, K-C Br J Cancer Molecular Diagnostics BACKGROUND: Diagnosis of oral cancer is conventionally carried out using white light endoscopy and histopathology of biopsy samples. However, oral tumours are mostly superficial and the lesion and its margins can be difficult to visualise under white light. We present clinical data on fluorescence diagnostic imaging of oral lesions using hypericin, a plant-based photosensitiser. METHODS: Fluorescence images of lesions and normal tissue were captured using an endoscope after hypericin administration. The images were analysed to extract their colour parameters, which, along with the red-to-blue intensity ratios, were analysed and used to discriminate between tissue types. The results were correlated with those from histopathology. RESULTS: The red-to-blue intensity ratio increased from normal to hyperplastic to cancerous tissue and was a good parameter to discriminate between these tissue types, with sensitivity and specificity levels of 90% and above. CONCLUSION: Our results show that hypericin fluorescence imaging has the potential to be used for the clinical diagnosis of oral cancer. Further study to enhance the clinical potential of this technique includes the development of a real-time image processing and analysis system interfaced to the endoscope to enable same-day cancer diagnosis and demarcation of lesion margins in a clinical setting. Nature Publishing Group 2009-11-03 2009-10-06 /pmc/articles/PMC2778520/ /pubmed/19809432 http://dx.doi.org/10.1038/sj.bjc.6605357 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Thong, P S P
Olivo, M
Chin, W W L
Bhuvaneswari, R
Mancer, K
Soo, K-C
Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title_full Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title_fullStr Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title_full_unstemmed Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title_short Clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
title_sort clinical application of fluorescence endoscopic imaging using hypericin for the diagnosis of human oral cavity lesions
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778520/
https://www.ncbi.nlm.nih.gov/pubmed/19809432
http://dx.doi.org/10.1038/sj.bjc.6605357
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