Braumann Ulf-Dietrich, Kuska Jens-Peer, Einenkel Jens, Horn Lars-Christian, Löffler Markus, Höckel Michael
Interdisciplinary Center for Bioinformatics, University Leipzig, Leipzig, Germany.
IEEE Trans Med Imaging. 2005 Oct;24(10):1286-307. doi: 10.1109/42.929614.
The analysis of the three-dimensional (3-D) structure of tumoral invasion fronts of carcinoma of the uterine cervix is the prerequisite for understanding their architectural-functional relationship. The variation range of the invasion patterns known so far reaches from a smooth tumor-host boundary surface to more diffusely spreading patterns, which all are supposed to have a different prognostic relevance. As a very decisive limitation of previous studies, all morphological assessments just could be done verbally referring to single histological sections. Therefore, the intention of this paper is to get an objective quantification of tumor invasion based on 3-D reconstructed tumoral tissue data. The image processing chain introduced here is capable to reconstruct selected parts of tumor invasion fronts from histological serial sections of remarkable extent (90-500 slices). While potentially gaining good accuracy and reasonably high resolution, microtome cutting of large serial sections especially may induce severe artifacts like distortions, folds, fissures or gaps. Starting from stacks of digitized transmitted light color images, an overall of three registration steps are the main parts of the presented algorithm. By this, we achieved the most detailed 3-D reconstruction of the invasion of solid tumors so far. Once reconstructed, the invasion front of the segmented tumor is quantified using discrete compactness.
分析子宫颈癌肿瘤浸润前沿的三维(3-D)结构是理解其结构-功能关系的前提条件。目前已知的浸润模式变化范围从光滑的肿瘤-宿主边界表面到更弥漫性扩散的模式,所有这些模式都被认为具有不同的预后相关性。作为以往研究的一个非常决定性的局限,所有形态学评估只能通过口头描述单个组织学切片来进行。因此,本文的目的是基于三维重建的肿瘤组织数据对肿瘤浸润进行客观量化。这里介绍的图像处理链能够从相当数量(90 - 500片)的组织学连续切片中重建肿瘤浸润前沿的选定部分。虽然有可能获得良好的准确性和相当高的分辨率,但对大量连续切片进行切片机切割尤其可能会产生严重的伪像,如变形、褶皱、裂缝或间隙。从数字化透射光彩色图像堆栈开始,总共三个配准步骤是所提出算法的主要部分。通过这种方式,我们实现了迄今为止实体肿瘤浸润最详细的三维重建。一旦重建完成,使用离散紧致性对分割肿瘤的浸润前沿进行量化。