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Comparative study of ex vivo probe‐based confocal laser endomicroscopy and light microscopy in lung cancer diagnostics
Author(s) -
Sorokina Anastasia,
Danilevskaya Olesya,
Averyanov Alexander,
Zabozlaev Fedor,
Sazonov Dmitry,
Yarmus Lonny,
Lee Hans J.
Publication year - 2014
Publication title -
respirology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 85
eISSN - 1440-1843
pISSN - 1323-7799
DOI - 10.1111/resp.12326
Subject(s) - pathology , medicine , ex vivo , lung cancer , adenocarcinoma , stromal cell , histopathology , lung , confocal , carcinoma , bronchoscopy , in vivo , cancer , radiology , biology , microbiology and biotechnology , geometry , mathematics
Background and objective Probe‐based confocal laser endoscopy (p CLE ) allows for real‐time non‐invasive histological imaging via bronchoscopy. Interpreting CLE images and correlating with traditional histopathology remains challenging. We performed an ex vivo study to evaluate the correlation between light microscopy findings and p CLE imaging of primary lung carcinoma. Methods Post‐lobectomy specimens for lung cancer nodules were examined ex vivo by p CLE . The examined areas were marked with brilliant green dye, and the surrounding tissues were stained by methylene blue dye. Lung tissue segments were resected and histopathological specimens were generated with 50‐μm thickness from the marked areas and stained with haematoxylin and eosin. Pathologists and pulmonologists reviewed the images for correlating features. Results Eighteen lobectomy specimens from 18 different patients were collected. Three primary features were observed in all samples using p CLE in the cancer surroundings: alveolar dystelectasis with thickening of alveolar walls, alveolar edema and a large amount of macrophages. The stromal and parenchymal components of the studied subtypes of non‐small‐cell lung cancer differed from each other. The stromal component for all nine adenocarcinoma specimens had a highly fluorescent field penetrated by dark hollows. All six squamous cell carcinoma specimens had the stromal component appeared as ‘biparously’ branching, highly fluorescent fibres. No stromal component was observed in any small‐cell carcinoma specimen, and at low power field, the cellular component was dominant with an observed light scattering pattern. Conclusions p CLE can identify lung carcinoma in ex vivo samples. Certain light microscopy features of lung carcinoma can be visualized with p CLE .