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Multimodal confocal mosaics enable high sensitivity and specificity in screening of in situ squamous cell carcinoma

机译:多模式共聚焦镶嵌技术可在筛查原位鳞状细胞癌中实现高灵敏度和特异性

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摘要

Screening cancer in excision margins with confocal microscopy may potentially save time and cost over the gold standard histopathology (H&E). However, diagnostic accuracy requires sufficient contrast and resolution to reveal pathological traits in a growing set of tumor types. Reflectance mode images structural details due to microscopic refractive index variation. Nuclear contrast with acridine orange fluorescence provides enhanced diagnostic value, but fails for in situ squamous cell carcinoma (SCC), where the cytoplasm is important to visualize. Combination of three modes [eosin (Eo) fluorescence, reflectance (R) and acridine orange (AO) fluorescence] enable imaging of cytoplasm, collagen and nuclei respectively. Toward rapid intra-operative pathological margin assessment to guide staged cancer excisions, multimodal confocal mosaics can image wide surgical margins (~1cm) with sub-cellular resolution and mimic the appearance of conventional H&E. Absorption contrast is achieved by alternating the excitation wavelength: 488nm (AO fluorescence) and 532nm (Eo fluorescence). Superposition and false-coloring of these modes mimics H&E, enabling detection of the carcinoma in situ in the epidermal layer The sum mosaic Eo+R is false-colored pink to mimic eosins' appearance in H&E, while the AO mosaic is false-colored purple to mimic hematoxylins' appearance in H&E. In this study, mosaics of 10 Mohs surgical excisions containing SCC in situ and 5 containing only normal tissue were subdivided for digital presentation equivalent to 4X histology. Of the total 16 SCC in situ multimodal mosaics and 16 normal cases presented, two reviewers made 1 and 2 (respectively) type-2 errors (false positives) but otherwise scored perfectly when using the confocal images to screen for the presence of SCC in situ as compared to the gold standard histopathology. Limitations to precisely mimic H&E included occasional elastin staining by AO. These results suggest that confocal mosaics may effectively guide staged SCC excisions in skin and other tissues.
机译:共聚焦显微镜筛查切除边缘的癌症可能比金标准组织病理学(H&E)节省时间和成本。但是,诊断准确性需要足够的对比度和分辨率,才能揭示出越来越多的肿瘤类型中的病理特征。反射率模式会由于微观折射率变化而对结构细节进行成像。 a啶橙荧光的核对比可提供增强的诊断价值,但对原发性鳞状细胞癌(SCC)无效,在那儿细胞质对于可视化很重要。三种模式的组合[曙红(Eo)荧光,反射率(R)和a啶橙(AO)荧光]分别使细胞质,胶原蛋白和细胞核成像。为了快速进行术中病理切缘评估,以指导分期癌切除,多模式共聚焦镶嵌术可在亚细胞分辨率下对宽阔的手术切缘(〜1cm)成像,并模仿传统的H&E外观。通过交替激发波长:488nm(AO荧光)和532nm(Eo荧光)来获得吸收对比。这些模式的叠加和错误着色可模仿H&E,从而能够在表皮层中原位检测癌变。总镶嵌Eo + R为错误颜色的粉红色,以模仿曙红在H&E中的外观,而AO马赛克为错误颜色的紫色模仿苏木精在H&E中的外观。在这项研究中,将包含原位SCC的10个Mohs手术切除和仅包含正常组织的5个Mohs手术切除的马赛克细分为等同于4X组织学的数字表示。在总共显示的16例SCC原位多模态马赛克和16例正常病例中,有2位审稿人分别发生了1和2型2错误(假阳性),但在使用共聚焦图像筛查原位SCC时得分较高与金标准组织病理学相比。精确模拟H&E的局限性包括AO偶尔进行的弹性蛋白染色。这些结果表明,共聚焦镶嵌术可以有效地指导皮肤和其他组织中的阶段性SCC切除。

著录项

  • 来源
    《Multimodal biomedical imaging IX》|2014年|893704.1-893704.9|共9页
  • 会议地点 San Francisco CA(US)
  • 作者单位

    Oregon Health Science University 3303 SW Bond Ave, Portland, OR 97239;

    Oregon Health Science University 3303 SW Bond Ave, Portland, OR 97239;

    Oregon Health Science University 3303 SW Bond Ave, Portland, OR 97239;

    Oregon Health Science University 3303 SW Bond Ave, Portland, OR 97239;

    Oregon Health Science University 3303 SW Bond Ave, Portland, OR 97239,The Rockefeller University Laboratory of Investigative Dermatology 1230 York Ave, New York, NY 10065;

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  • 正文语种 eng
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