Standardization of whole slide image morphologic assessment with definition of a new application: Digital slide dynamic morphometry

Background: In histopathology, the quantitative assessment of various morphologic features is based on methods originally conceived on specific areas observed through the microscope used. Failure to reproduce the same reference field of view using a different microscope will change the score assesse...

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Published inJournal of pathology informatics Vol. 2; no. 1; p. 48
Main Authors Puppa, Giacomo, Risio, Mauro, Sheahan, Kieran, Vieth, Michael, Zlobec, Inti, Lugli, Alessandro, Pecori, Sara, Wang, Lai Mun, Langner, Cord, Mitomi, Hiroyuki, Nakamura, Takatoshi, Watanabe, Masahiko, Ueno, Hideki, Chasle, Jacques, Senore, Carlo, Conley, Stephen A., Herlin, Paulette, Lauwers, Gregory Y.
Format Journal Article
LanguageEnglish
Published India Elsevier Inc 2011
Medknow Publications and Media Pvt. Ltd
Medknow Publications & Media Pvt Ltd
Elsevier
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Summary:Background: In histopathology, the quantitative assessment of various morphologic features is based on methods originally conceived on specific areas observed through the microscope used. Failure to reproduce the same reference field of view using a different microscope will change the score assessed. Visualization of a digital slide on a screen through a dedicated viewer allows selection of the magnification. However, the field of view is rectangular, unlike the circular field of optical microscopy. In addition, the size of the selected area is not evident, and must be calculated. Materials and Methods: A digital slide morphometric system was conceived to reproduce the various methods published for assessing tumor budding in colorectal cancer. Eighteen international experts in colorectal cancer were invited to participate in a web-based study by assessing tumor budding with five different methods in 100 digital slides. Results: The specific areas to be tested by each method were marked by colored circles. The areas were grouped in a target-like pattern and then saved as an .xml file. When a digital slide was opened, the .xml file was imported in order to perform the measurements. Since the morphometric tool is composed of layers that can be freely moved on top of the digital slide, the technique was named digital slide dynamic morphometry. Twelve investigators completed the task, the majority of them performing the multiple evaluations of each of the cases in less than 12 minutes. Conclusions: Digital slide dynamic morphometry has various potential applications and might be a useful tool for the assessment of histologic parameters originally conceived for optical microscopy that need to be quantified.
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ISSN:2153-3539
2229-5089
2153-3539
DOI:10.4103/2153-3539.86830