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Multiparametric Analysis of Fine Needle Aspirate Biopsies from Parotid Tumors by Laser Scanning Cytometry (LSC)

机译:激光扫描细胞术中腮腺肿瘤的细针吸入活组织检查的多分析分析(LSC)

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In order minimize hospitalization and morbidity with optimized therapy for a patient with a tumor of the parotid gland a malignancy must be confirmed or excluded as soon as possible. Up to now, non- and minimal-invasive methods do not yield this information. For fine needle aspirate biopsies (FNABs), analysis by a specialized cytologist yields subjective and qualitative but not objective and quantitative data. LSC is a semi-automated microscope-based technology and offers ideal prerequisites for the analysis of specimens fixed on a slide. We have established an assay for FNABs from parotid gland tumors. Cells are stained for cytokeratin and DNA. The analysis quantitatively determines the ploidy of the cells and the degree of condensation of the DNA; on this basis the percentage of cells undergoing mitosis can be determined. Subsequently the cells are stained by H&E and are re-localized on the slide at their fixed position. Micrographs are taken for objective documentation of the cells' morphology. Using this assay FNABs from parotid gland tumors were analyzed; tumors that were diagnosed as benign by routine histopathology showed no aneuploidy whereas malignant tumors were aneuploid. This preliminary study demonstrates the capacities of LSC for minimal-invasive assays yielding quantitative and objective data.
机译:为了使患者对患者的患者的优化治疗最大限度地减少治疗腮腺的患者,这种恶性必须尽快确认或排除恶性肿瘤。到目前为止,非侵入性方法不产生此信息。对于细针吸气活组织检查(FNAB),专用细胞学家的分析产生主观和定性但不客观和定量数据。 LSC是一种基于半自动的显微镜技术,提供了理想的先决条件,用于分析固定在幻灯片上的标本。我们已经为来自腮腺肿瘤的FNAB进行了分析。细胞染成细胞角蛋白和DNA。分析定量地确定细胞的倍率和DNA的缩合程度;在此基础上,可以确定接受有丝分裂的细胞百分比。随后,细胞由H&E染色,并在其固定位置重新定位在滑动件上。显微照片用于客观记录细胞的形态。分析来自腮腺肿瘤的该测定法,分析;被常规组织病理学被诊断为良性的肿瘤显示出一种非整倍性的,而恶性肿瘤是一种非洲倍性。该初步研究表明LSC的能力对于产生定量和客观数据的最小侵入性测定。

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