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Volume 71, Issue 1, Pages 35-43 (January 2010)


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Comprehensive imaging of gastroesophageal biopsy samples by spectrally encoded confocal microscopy

DongKyun Kang, PhD, Melissa J. Suter, PhD, Caroline Boudoux, PhD, Hongki Yoo, PhD, Patrick S. Yachimski, MD, William P. Puricelli, RN, Norman S. Nishioka, MD, Mari Mino-Kenudson, MD, Gregory Y. Lauwers, MD, Brett E. Bouma, PhD, Guillermo J. Tearney, MD, PhDCorresponding Author Information

Received 15 May 2009; accepted 23 August 2009. published online 18 November 2009.

Background

Spectrally encoded confocal microscopy (SECM) is a high-speed reflectance confocal microscopy technique that has the potential to be used for acquiring comprehensive images of the entire distal esophagus endoscopically with subcellular resolution.

Objective

The goal of this study was to demonstrate large-area SECM in upper GI tissues and to determine whether the images contain microstructural information that is useful for pathologic diagnosis.

Design

A feasibility study.

Setting

Gastrointestinal Unit, Massachusetts General Hospital.

Patients

Fifty biopsy samples from 36 patients undergoing routine EGD were imaged by SECM, in their entirety, immediately after their removal.

Results

The microstructure seen in the SECM images was similar to that seen by histopathology. Gastric cardia mucosa was clearly differentiated from squamous mucosa. Gastric fundic/body type mucosa showed more tightly packed glands than gastric cardia mucosa. Fundic gland polyps showed cystically dilated glands lined with cuboidal epithelium. The presence of intraepithelial eosinophils was detected with the cells demonstrating a characteristic bilobed nucleus. Specialized intestinal metaplasia was identified by columnar epithelium and the presence of goblet cells. Barrett's esophagus (BE) with dysplasia was differentiated from specialized intestinal metaplasia by the loss of nuclear polarity and disorganized glandular architecture.

Limitations

Ex vivo, descriptive study.

Conclusions

Large-area SECM images of gastroesophageal biopsy samples enabled the visualization of both subcellular and architectural features of various upper GI mucosal types and were similar to the corresponding histopathologic slides. These results suggest that the development of an endoscopic SECM probe is merited.

Boston, Massachusetts, USA

Current affiliations: Wellman Center for Photomedicine (D.K., M.J.S., H.Y., B.E.B., G.J.T.), Department of Dermatology (D.K., M.J.S., H.Y., B.E.B.), Gastrointestinal Unit (W.P.P., N.S.N.), and Department of Pathology (M.M.K., G.Y.L., G.J.T.), Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, Department of Engineering Physics (C.B.), Ecole Polytechnique Montreal, Montreal, Quebec, Canada, Division of Gastroenterology, Hepatology, and Nutrition (P.S.Y.), Vanderbilt University Medical Center, Nashville, Tennessee, USA

Corresponding Author InformationReprint requests: Guillermo J. Tearney, MD, PhD, Harvard Medical School, Massachusetts General Hospital, and Wellman Center for Photomedicine, 40 Blossom Street, BAR 703, Boston, MA 02114.

 DISCLOSURE: This research was supported by National Institutes of Health/National Cancer Institute (grant number R21CA122161). All authors disclosed no financial relationships relevant to this publication.

PII: S0016-5107(09)02426-2

doi:10.1016/j.gie.2009.08.026


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