Polarised light scanner for digital pathology.

IF 3.4 3区 医学 Q1 PATHOLOGY
Dunia Al Sheikhyaqoob, André Oliveira, Manuel Fella, Don Laferty, Gerald Niedobitek
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引用次数: 0

Abstract

Digital pathology is rapidly transforming diagnostic pathology by allowing remote work and integration of artificial intelligence solutions. Nevertheless, certain technical issues remain to be resolved. Notably, digital images captured by conventional scanners cannot be subjected to polarised light analysis [1]. We have therefore studied if images obtained using the Glissando POL Brightfield and Polarised Light Scanner are comparable to those obtained using conventional polarised light microscopy. Hematoxylin and eosin stained sections from 75 cases, including cases of amyloidosis, periprosthetic membranes, foreign body granulomas, gout, pseudogout, and breast tissues with calcium oxalate crystals were examined using both, a polarised light microscope and the Glissando POL scanner. Representative digital images were acquired for comparison. We here show that in all settings, the images obtained by conventional polarised light microscopy and using the Glissando POL scanner were comparable. We conclude that the Glissando POL scanner can be safely integrated into a digital pathology workflow.

数字病理偏振光扫描仪。
数字病理学通过允许远程工作和整合人工智能解决方案,正在迅速改变病理诊断。然而,某些技术问题仍有待解决。值得注意的是,传统扫描仪采集的数字图像无法进行偏振光分析[1]。因此,我们研究了使用 Glissando POL 明视野和偏振光扫描仪获得的图像是否与使用传统偏振光显微镜获得的图像具有可比性。我们使用偏振光显微镜和 Glissando POL 扫描仪对 75 个病例的血色素和伊红染色切片进行了检查,其中包括淀粉样变性、假体周围膜、异物肉芽肿、痛风、假性痛风和带有草酸钙结晶的乳腺组织。我们还获取了具有代表性的数字图像进行对比。我们在此表明,在所有情况下,使用传统偏光显微镜和 Glissando POL 扫描仪获得的图像都具有可比性。我们的结论是,Glissando POL 扫描仪可以安全地集成到数字病理学工作流程中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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