论文标题
限制的多形演化,用于重叠的细胞质分段
Constrained Multi-shape Evolution for Overlapping Cytoplasm Segmentation
论文作者
论文摘要
细分细胞在宫颈涂片图像中的重叠细胞质是临床上必不可少的任务,用于定量测量细胞水平特征以诊断宫颈癌。但是,这项任务仍然具有挑战性,这主要是由于重叠区域中强度(或颜色)信息的缺乏。 Although shape prior-based models that compensate intensity deficiency by introducing prior shape information (shape priors) about cytoplasm are firmly established, they often yield visually implausible results, mainly because they model shape priors only by limited shape hypotheses about cytoplasm, exploit cytoplasm-level shape priors alone, and impose no shape constraint on the resulting shape of the cytoplasm.在本文中,我们提出了一种新型且有效的基于形状的基于形状的方法,称为受约束多形演化,该方法通过共同将每个细胞质的形状共同演变为由建模的形状priors指导的每个细胞质的形状,从而在团块中分布整个重叠的细胞质。我们通过无限大的假设集对局部形状先验(细胞质 - 级)进行建模,该假说集包含所有可能的细胞质形状。在形状的演化中,我们不仅引入了建模的局部形状先验,还可以通过考虑通过考虑团块中的细胞肿瘤的相互形状约束来弥补分割的强度缺陷。我们还将每种进化中的结果形状限制为建立形状假设集,以进一步降低令人难以置信的分割结果。我们在两个典型的宫颈涂片数据集中评估了所提出的方法,并且广泛的实验结果表明,该方法有效地分割了重叠的细胞质,从而始终优于最先进的方法。
Segmenting overlapping cytoplasm of cells in cervical smear images is a clinically essential task, for quantitatively measuring cell-level features in order to diagnose cervical cancer. This task, however, remains rather challenging, mainly due to the deficiency of intensity (or color) information in the overlapping region. Although shape prior-based models that compensate intensity deficiency by introducing prior shape information (shape priors) about cytoplasm are firmly established, they often yield visually implausible results, mainly because they model shape priors only by limited shape hypotheses about cytoplasm, exploit cytoplasm-level shape priors alone, and impose no shape constraint on the resulting shape of the cytoplasm. In this paper, we present a novel and effective shape prior-based approach, called constrained multi-shape evolution, that segments all overlapping cytoplasms in the clump simultaneously by jointly evolving each cytoplasm's shape guided by the modeled shape priors. We model local shape priors (cytoplasm--level) by an infinitely large shape hypothesis set which contains all possible shapes of the cytoplasm. In the shape evolution, we compensate intensity deficiency for the segmentation by introducing not only the modeled local shape priors but also global shape priors (clump--level) modeled by considering mutual shape constraints of cytoplasms in the clump. We also constrain the resulting shape in each evolution to be in the built shape hypothesis set, for further reducing implausible segmentation results. We evaluated the proposed method in two typical cervical smear datasets, and the extensive experimental results show that the proposed method is effective to segment overlapping cytoplasm, consistently outperforming the state-of-the-art methods.