Mackin R W, Roysam B, Holmes T J, Turner J N
Department of Electrical, Computer and Systems Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180.
Anal Quant Cytol Histol. 1993 Dec;15(6):405-17.
Methods are presented for automated analysis of thick and heavily overlapped regions of cytologic preparations, such as cervical/vaginal smears. Current systems are unable to process these regions although they contain diagnostically valuable information. We argue that analysis of such regions is inherently a three-dimensional (3-D) problem that cannot be solved reliably with conventional two-dimensional methods. Furthermore, this issue cannot be side-stepped by special thin preparation methods. Even with 3-D imaging, analysis of these regions is complicated by the high variability in the image gray level and textural features resulting from the uncontrollable cell overlaps and folds and large computational requirements. A novel approach based on 3-D imaging and adaptive 3-D analysis algorithms based on the principles of localization, adaptive data reduction and clustering theory is presented. It was successful in detecting and separating deeply embedded and overlapping nuclei, cytoplasmic folds and creases in thick and overlapped regions of conventional smears and special thin preparations.
本文介绍了用于自动分析细胞学标本(如宫颈/阴道涂片)中厚且严重重叠区域的方法。当前系统无法处理这些区域,尽管它们包含有诊断价值的信息。我们认为,对此类区域的分析本质上是一个三维(3-D)问题,传统的二维方法无法可靠地解决。此外,特殊的薄制片方法也无法回避这个问题。即使采用三维成像,由于细胞不可控的重叠、折叠以及较大的计算需求导致图像灰度和纹理特征高度可变,对这些区域的分析也很复杂。本文提出了一种基于三维成像以及基于定位、自适应数据约简和聚类理论的自适应三维分析算法的新方法。该方法成功地检测并分离了传统涂片和特殊薄制片厚且重叠区域中深深嵌入和重叠的细胞核、细胞质褶皱和折痕。