Kronqvist P, Collan Y, Kuopio T, Kujari H
Department of Pathology, University of Turku, Finland.
Mod Pathol. 1995 Feb;8(2):187-92.
We studied nuclear morphometry of human breast cancer with special emphasis on two sources of variation: freezing prior to fixation and selection of measured objects on the basis of different sampling rules. Samples of 147 histologically verified invasive breast cancer cases were examined with a computer-based image overlay drawing system. Thirty-eight of the 147 samples of tissue frozen before embedding in paraffin were analyzed separately. Among the latter we found shrinkage of 35% and 46% (depending on the sampling rule) of the nuclear profile area as compared with samples not frozen before the standard tissue processing. These findings confirm that nuclear morphometry results from frozen and unfrozen tissue are not comparable. Frozen tissue later embedded in paraffin should not be used with prognostication models based on traditionally fixed tissue. In morphometry we applied two sampling rules that differed in the criteria used for selecting nuclei for measurement. We registered a significant difference in nuclear size and in the variation of nuclear size between the two sampling methods. Of the morphometric features studied, nuclear area was affected most. Finally, we examined the two sampling rules in light of the established prognosticators in breast cancer: tumor size, axillary lymph node status, and the Multivariate Prognostic Index (MPI). The two sampling rules resulted in different distributions of morphometric results in the prognostic groups. Our findings emphasize the significance of the sources of variation in nuclear morphometry. They also stress the need for well-standardized morphometric methods in predicting the outcome of breast cancer.
我们研究了人类乳腺癌的细胞核形态测量学,特别关注两个变异来源:固定前的冷冻以及基于不同采样规则对测量对象的选择。使用基于计算机的图像叠加绘图系统对147例经组织学证实的浸润性乳腺癌病例样本进行了检查。对147个石蜡包埋前冷冻的组织样本中的38个进行了单独分析。在后者中,我们发现与标准组织处理前未冷冻的样本相比,核轮廓面积缩小了35%和46%(取决于采样规则)。这些发现证实,冷冻组织和未冷冻组织的细胞核形态测量结果不可比。后来石蜡包埋的冷冻组织不应与基于传统固定组织的预后模型一起使用。在形态测量学中,我们应用了两种在选择测量细胞核的标准上不同的采样规则。我们记录了两种采样方法在核大小以及核大小变异方面的显著差异。在所研究的形态测量特征中,核面积受影响最大。最后,我们根据已确立的乳腺癌预后指标:肿瘤大小、腋窝淋巴结状态和多变量预后指数(MPI),对这两种采样规则进行了研究。这两种采样规则在预后组中导致了形态测量结果的不同分布。我们的发现强调了细胞核形态测量学中变异来源的重要性。它们还强调了在预测乳腺癌预后时采用标准化良好的形态测量方法的必要性。