Literature DB >> 15568948

Detection and diagnosis of oral neoplasia with an optical coherence microscope.

A L Clark1, A Gillenwater, R Alizadeh-Naderi, A K El-Naggar, R Richards-Kortum.   

Abstract

The use of high resolution, in vivo optical imaging may offer a clinically useful adjunct to standard histopathologic techniques. A pilot study was performed to investigate the diagnostic capabilities of optical coherence microscopy (OCM) to discriminate between normal and abnormal oral tissue. Our objective is to determine whether OCM, a technique combining the subcellular resolution of confocal microscopy with the coherence gating and heterodyne detection of optical coherence tomography, has the same ability as confocal microscopy to detect morphological changes present in precancers of the epithelium while providing superior penetration depths. We report our results using OCM to characterize the features of normal and neoplastic oral mucosa excised from 13 subjects. Specifically, we use optical coherence and confocal microscopic images obtained from human oral biopsy specimens at various depths from the mucosal surface to examine the optical properties that distinguish normal and neoplastic oral mucosa. An analysis of penetration depths achieved by the OCM and its associated confocal arm found that the OCM consistently imaged more deeply. Extraction of scattering coefficients from reflected nuclear intensity is successful in nonhyperkeratotic layers and shows differentiation between scattering properties of normal and dysplastic epithelium and invasive cancer. Copyright 2004 Society of Photo-Optical Instrumentation Engineers.

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Year:  2004        PMID: 15568948      PMCID: PMC2773167          DOI: 10.1117/1.1805558

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  36 in total

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2.  Optical coherence tomography of the esophagus and proximal stomach in health and disease.

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3.  Light scattering from normal and dysplastic cervical cells at different epithelial depths: finite-difference time-domain modeling with a perfectly matched layer boundary condition.

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Journal:  J Biomed Opt       Date:  2003-07       Impact factor: 3.170

4.  An optical coherence microscope for 3-dimensional imaging in developmental biology.

Authors:  B Hoeling; A Fernandez; R Haskell; E Huang; W Myers; D Petersen; S Ungersma; R Wang; M Williams; S Fraser
Journal:  Opt Express       Date:  2000-03-27       Impact factor: 3.894

5.  High-resolution imaging of gynecologic neoplasms using optical coherence tomography.

Authors:  C Pitris; A Goodman; S A Boppart; J J Libus; J G Fujimoto; M E Brezinski
Journal:  Obstet Gynecol       Date:  1999-01       Impact factor: 7.661

6.  Detection of clinically amelanotic malignant melanoma and assessment of its margins by in vivo confocal scanning laser microscopy.

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7.  Near real time confocal microscopy of cultured amelanotic cells: sources of signal, contrast agents and limits of contrast.

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9.  In vivo endoscopic optical coherence tomography of esophagitis, Barrett's esophagus, and adenocarcinoma of the esophagus.

Authors:  S Jäckle; N Gladkova; F Feldchtein; A Terentieva; B Brand; G Gelikonov; V Gelikonov; A Sergeev; A Fritscher-Ravens; J Freund; U Seitz; S Schröder; N Soehendra
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  21 in total

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Journal:  Biomed Opt Express       Date:  2015-08-21       Impact factor: 3.732

2.  Autofluorescence and diffuse reflectance spectroscopy of oral epithelial tissue using a depth-sensitive fiber-optic probe.

Authors:  Richard A Schwarz; Wen Gao; Dania Daye; Michelle D Williams; Rebecca Richards-Kortum; Ann M Gillenwater
Journal:  Appl Opt       Date:  2008-02-20       Impact factor: 1.980

3.  Monte Carlo model to describe depth selective fluorescence spectra of epithelial tissue: applications for diagnosis of oral precancer.

Authors:  Ina Pavlova; Crystal Redden Weber; Richard A Schwarz; Michelle Williams; Adel El-Naggar; Ann Gillenwater; Rebecca Richards-Kortum
Journal:  J Biomed Opt       Date:  2008 Nov-Dec       Impact factor: 3.170

4.  Rapid staining and imaging of subnuclear features to differentiate between malignant and benign breast tissues at a point-of-care setting.

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5.  Fluorescence lifetime imaging and reflectance confocal microscopy for multiscale imaging of oral precancer.

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6.  Dynamic multicomponent engineered tissue reorganization and matrix deposition measured with an integrated nonlinear optical microscopy-optical coherence microscopy system.

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7.  Analyzing spatial correlations in tissue using angle-resolved low coherence interferometry measurements guided by co-located optical coherence tomography.

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8.  Cellular resolution ex vivo imaging of gastrointestinal tissues with optical coherence microscopy.

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9.  Model-based quantitative optical biopsy in multilayer in vitro soft tissue models for whole field assessment of nonmelanoma skin cancer.

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10.  High speed optical coherence microscopy with autofocus adjustment and a miniaturized endoscopic imaging probe.

Authors:  Aaron D Aguirre; Juergen Sawinski; Shu-Wei Huang; Chao Zhou; Winfried Denk; James G Fujimoto
Journal:  Opt Express       Date:  2010-03-01       Impact factor: 3.894

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