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dc.contributor.authorLee, Hsiang-Chieh
dc.contributor.authorZhou, Chao
dc.contributor.authorWang, Yihong
dc.contributor.authorAguirre, Aaron Dominic
dc.contributor.authorTsai, Tsung-Han
dc.contributor.authorCohen, David W.
dc.contributor.authorConnolly, James L.
dc.contributor.authorFujimoto, James G.
dc.date.accessioned2010-09-14T16:34:09Z
dc.date.available2010-09-14T16:34:09Z
dc.date.issued2010-02
dc.date.submitted2010-01
dc.identifier.issn0277-786X
dc.identifier.urihttp://hdl.handle.net/1721.1/58530
dc.description.abstractExcisional biopsy is the current gold standard for disease diagnosis; however, it requires a relatively long processing time and it may also suffer from unacceptable false negative rates due to sampling errors. Optical coherence tomography (OCT) is a promising imaging technique that provide real-time, high resolution and three-dimensional (3D) images of tissue morphology. Optical coherence microscopy (OCM) is an extension of OCT, combining both the coherence gating and the confocal gating techniques. OCM imaging achieves cellular resolution with deeper imaging depth compared to confocal microscopy. An integrated OCT/OCM imaging system can provide co-registered multiscale imaging of tissue morphology. 3D-OCT provides architectural information with a large field of view and can be used to find regions of interest; while OCM provides high magnification to enable cellular imaging. The integrated OCT/OCM system has an axial resolution of <4um and transverse resolutions of 14um and <2um for OCT and OCM, respectively. In this study, a wide range of human pathologic specimens, including colon (58), thyroid (43), breast (34), and kidney (19), were imaged with OCT and OCM within 2 to 6 hours after excision. The images were compared with H & E histology to identify characteristic features useful for disease diagnosis. The feasibility of visualizing human pathology using integrated OCT/OCM was demonstrated in the pathology laboratory settings.en_US
dc.language.isoen_US
dc.publisherSPIEen_US
dc.relation.isversionofhttp://dx.doi.org/10.1117/12.843283en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSPIEen_US
dc.subjectOptical coherence tomographyen_US
dc.subjectoptical coherence microscopyen_US
dc.subjecthuman pathologyen_US
dc.titleIntegrated Optical Coherence Tomography and Optical Coherence Microscopy Imaging of Human Pathologyen_US
dc.typeArticleen_US
dc.identifier.citationLee, Hsiang-Chieh et al. “Integrated optical coherence tomography and optical coherence microscopy imaging of human pathology.” Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XVII. Ed. Jose-Angel Conchello et al. San Francisco, California, USA: SPIE, 2010. 75700J-8. ©2010 COPYRIGHT SPIE--The International Society for Optical Engineering.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.approverFujimoto, James G.
dc.contributor.mitauthorLee, Hsiang-Chieh
dc.contributor.mitauthorZhou, Chao
dc.contributor.mitauthorAguirre, Aaron Dominic
dc.contributor.mitauthorTsai, Tsung-Han
dc.contributor.mitauthorFujimoto, James G.
dc.relation.journalProceedings of SPIE--the International Society for Optical Engineering; v.7570en_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLee, Hsiang-Chieh; Zhou, Chao; Wang, Yihong; Aquirre, Aaron D.; Tsai, Tsung-Han; Cohen, David W.; Connolly, James L.; Fujimoto, James G.en
dc.identifier.orcidhttps://orcid.org/0000-0002-0828-4357
dc.identifier.orcidhttps://orcid.org/0000-0002-2976-6195
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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