High-resolution imaging in Barrett's esophagus: a novel, low-cost endoscopic microscope.

Timothy J Muldoon, Sharmila Anandasabapathy, Dipen Maru, Rebecca Richards-Kortum
Author Information
  1. Timothy J Muldoon: Department of Bioengineering, Rice University, Houston, Texas 77005, USA.

Abstract

BACKGROUND: This report describes the clinical evaluation of a novel, low-cost, high-resolution endoscopic microscope for obtaining fluorescent images of the cellular morphology of the epithelium of regions of the esophagus with Barrett's metaplasia. This noninvasive point imaging system offers a method for obtaining real-time histologic information during endoscopy.
OBJECTIVE: The objective of this study was to compare images taken with the fiberoptic endoscopic microscope with standard histopathologic examination.
DESIGN: Feasibility study.
SETTING: The University of Texas M.D. Anderson Cancer Center Department of Gastroenterology. PATIENTS, INTERVENTIONS, AND MAIN OUTCOME MEASUREMENTS: The tissue samples studied in this report were obtained by endoscopic resection from patients with previous diagnoses of either high-grade dysplasia or esophageal adenocarcinoma.
RESULTS: Three distinct tissue types were observed ex vivo with the endoscopic microscope: normal squamous mucosa, Barrett's metaplasia, and high-grade dysplasia. Squamous tissue was identified by bright nuclei surrounded by dark cytoplasm in an ordered pattern. Barrett's metaplasia could be identified by large glandular structures with intact nuclear polarity. High-grade dysplasia was visualized as plentiful, irregular glandular structures and loss of nuclear polarity. Standard histopathologic examination of study samples confirmed the results obtained by the endoscopic microscope.
LIMITATIONS: The endoscopic microscope probe had to be placed into direct contact with tissue.
CONCLUSIONS: It was feasible to obtain high-resolution histopathologic information using the endoscopic microscope device. Future improvement and integration with widefield endoscopic techniques will aid in improving the sensitivity of detection of dysplasia and early cancer development in the esophagus.

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Grants

  1. CA103830/NCI NIH HHS
  2. R01 EB007594-02/NIBIB NIH HHS
  3. R01 CA103830-05/NCI NIH HHS
  4. P30 DK56338/NIDDK NIH HHS
  5. P30 DK056338/NIDDK NIH HHS
  6. R01 CA103830/NCI NIH HHS
  7. R01 EB007594/NIBIB NIH HHS
  8. R01 EB002179/NIBIB NIH HHS

MeSH Term

Barrett Esophagus
Contrast Media
Endoscopy, Digestive System
Feasibility Studies
Humans
Metaplasia
Microscopy, Confocal

Chemicals

Contrast Media

Word Cloud

Created with Highcharts 10.0.0endoscopicmicroscopeBarrett'stissuedysplasiametaplasiastudyhistopathologicreportnovellow-costhigh-resolutionobtainingimagesesophagusimaginginformationexaminationsamplesobtainedhigh-gradeidentifiedglandularstructuresnuclearpolarityBACKGROUND:describesclinicalevaluationfluorescentcellularmorphologyepitheliumregionsnoninvasivepointsystemoffersmethodreal-timehistologicendoscopyOBJECTIVE:objectivecomparetakenfiberopticstandardDESIGN:FeasibilitySETTING:UniversityTexasMDAndersonCancerCenterDepartmentGastroenterologyPATIENTSINTERVENTIONSANDMAINOUTCOMEMEASUREMENTS:studiedresectionpatientspreviousdiagnoseseitheresophagealadenocarcinomaRESULTS:Threedistincttypesobservedexvivomicroscope:normalsquamousmucosaSquamousbrightnucleisurroundeddarkcytoplasmorderedpatternlargeintactHigh-gradevisualizedplentifulirregularlossStandardconfirmedresultsLIMITATIONS:probeplaceddirectcontactCONCLUSIONS:feasibleobtainusingdeviceFutureimprovementintegrationwidefieldtechniqueswillaidimprovingsensitivitydetectionearlycancerdevelopmentHigh-resolutionesophagus:

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