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  4. In vivo autofluorescence spectroscopy of oral premalignant and malignant lesions: Distortion of fluorescence intensity by submucous fibrosis
 
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In vivo autofluorescence spectroscopy of oral premalignant and malignant lesions: Distortion of fluorescence intensity by submucous fibrosis

Journal
Lasers in Surgery and Medicine
Journal Volume
33
Journal Issue
1
Pages
40-47
Date Issued
2003
Author(s)
Tsai T.
HSIN-MING CHEN  
Wang C.-Y.
JUI-CHANG TSAI  
Chen C.-T.
CHUN-PIN CHIANG  
DOI
10.1002/lsm.10180
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0042267824&doi=10.1002%2flsm.10180&partnerID=40&md5=354ca80ea5861a5ec127e160f43097f2
https://scholars.lib.ntu.edu.tw/handle/123456789/465282
Abstract
Background and Objectives: To test whether autofluorescence spectroscopy can be used for the diagnosis of oral neoplasia in a high-risk population, we characterized the in vivo autofluorescence spectra from oral submucous fibrosis (OSF) lesions and oral premalignant and malignant lesions in both OSF and non-OSF patients. Study Design/Materials and Methods: Autofluorescence emission spectra were measured under the excitation wavelength of 330 nm, using a Xenon lamp-based fluorospectrometer coupled to a handheld optical fiber probe. Autofluorescence spectroscopies were analyzed among patients with OSF lesions, and oral lesions of epithelial hyperkeratosis (EH), epithelial dysplasia (ED), and squamous cell carcinomas (SCC) and normal oral mucosa (NOM) of healthy volunteers. Results: We found that the most intensely autofluorescence emission peaks occurred at 380 nm and 460 nm. For comparing the spectral patterns among different groups of oral lesions and NOM, ratios of the area under the spectrum of 460 ± 10 nm to that under the spectrum of 380 ± 10 nm (denoted as A460 ± 10 nm/A380 ± 10 nm) were calculated. The mean ratio values increased gradually from OSF to NOM, to EH and ED, and to SCC. The ANOVA test showed significant differences in the ratio value among all categories of samples (P < 0.01). On the other hand, we found that EH, ED, and SCC lesions on OSF patients had distorted autofluorescence intensity. The mean ratio values of EH, ED, and SCC between non-OSF and OSF patients show significant differences. Furthermore, an ANOVA test showed NOM is not distinguishable from EH and ED lesions on oral fibrotic mucosa (P > 0.05). Conclusions: Autofluorescence spectroscopy can be used to diagnose EH, ED, and SCC lesions in non-OSF patients but not in OSF patients. ? 2003 Wiley-Liss, Inc.
SDGs

[SDGs]SDG3

Other Subjects
article; autofluorescence; controlled study; dysplasia; fibrosis; fluorescence spectroscopy; head and neck cancer; human; human tissue; hyperkeratosis; major clinical study; mouth cancer; mouth mucosa; precancer; priority journal; spectroscopy; squamous cell carcinoma; Carcinoma, Squamous Cell; Diagnosis, Differential; Humans; Mouth Neoplasms; Oral Submucous Fibrosis; Precancerous Conditions; Reproducibility of Results; Spectrometry, Fluorescence
Type
journal article

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