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星形细胞瘤的立体定向活检。定量染色质模式描述所提供的诊断信息。

Stereotactic biopsies from astrocytic tumors. Diagnostic information contributed by the quantitative chromatin pattern description.

作者信息

Salmon I, Rorive S, Camby I, Decaestecker C, Pirotte B, Rombaut K, Haot J, Pasteels J L, Brotchi J, Kiss R

机构信息

Service d'Anatomie Pathologique, Hopital Erasme, Brussels, Belgium.

出版信息

Anal Quant Cytol Histol. 1995 Oct;17(5):332-43.

PMID:8534336
Abstract

OBJECTIVE

To reduce the problem of heterogeneity in astrocytic tumors by means of computer-assisted microscope analysis of Feulgen-stained nuclei.

STUDY DESIGN

Thirty-eight glial tumors for which we obtained 227 stereotactic biopsies were subjected to digital cell image analysis of Feulgen-stained nuclei. This series of 38 glial tumors included 36 supratentorial astrocytic tumors (13 astrocytomas, 7 anaplastic astrocytomas and 16 glioblastoma multiformes) and 2 grade 3 astrocytic tumors of the cerebellum.

RESULTS

The results suggest a new methodology, enabling the biologic characteristics of the brain parenchymal area surrounding a given glial tumor to be characterized. This methodology relies on the performance of three successive steps. The first is quantitative characterization of nuclear morphology and its chromatin pattern by means of 15 morphonuclear variables. This characterization is carried out by means of the computer-assisted microscope analysis of Feulgen-stained nuclei. The second step consists of setting up morphonuclear data banks, with each process giving the precise portrait of a given cell nuclear population. This process is carried out by means of multivariate analysis, taking into account the 15 variables mentioned above. Multivariate analysis includes principal components analysis followed by the canonical transformation of the data. The third step consists of testing unknown cases against these morphonuclear data banks. This is carried out by means of linear discriminant analysis, which enables the various cell nuclear types in the stereotactic biopsy to be quantified.

CONCLUSION

The present methodology makes it possible to investigate whether infiltrating tumor cells are present in or absent from the parenchymal brain area surrounding a glial tumor. It can therefore contribute additional information to that contributed by computed tomography and/or magnetic resonance imaging with respect to the precise delineation of the volume of a brain tumor. This delineation must be as precise as possible to allow total surgical resection of the tumor and prevention of its recurrence.

摘要

目的

通过对福尔根染色细胞核进行计算机辅助显微镜分析,减少星形细胞瘤中的异质性问题。

研究设计

对38例胶质肿瘤进行了福尔根染色细胞核的数字细胞图像分析,我们从这些肿瘤中获取了227份立体定向活检样本。这38例胶质肿瘤系列包括36例幕上星形细胞瘤(13例星形细胞瘤、7例间变性星形细胞瘤和16例多形性胶质母细胞瘤)以及2例小脑3级星形细胞瘤。

结果

结果提示了一种新方法,能够对给定胶质肿瘤周围脑实质区域的生物学特征进行表征。该方法依赖于三个连续步骤的实施。第一步是通过15个形态核变量对核形态及其染色质模式进行定量表征。这种表征是通过对福尔根染色细胞核的计算机辅助显微镜分析来进行的。第二步包括建立形态核数据库,每个过程给出给定细胞核群体的精确画像。该过程通过多变量分析来进行,考虑到上述15个变量。多变量分析包括主成分分析,随后是数据的典型变换。第三步包括针对这些形态核数据库对未知病例进行测试。这是通过线性判别分析来进行的,它能够对立体定向活检中的各种细胞核类型进行量化。

结论

目前的方法能够研究胶质肿瘤周围脑实质区域是否存在浸润性肿瘤细胞。因此,它可以为计算机断层扫描和/或磁共振成像在精确描绘脑肿瘤体积方面提供的信息增添额外信息。这种描绘必须尽可能精确,以实现肿瘤的完全手术切除并预防其复发。

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