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小脑星形细胞瘤。第一部分。大体及显微镜下特征。

Cerebellar astrocytomas. Part I. Macroscopic and microscopic features.

作者信息

Ilgren E B, Stiller C A

机构信息

Department of Neuropathology, Radcliffe Infirmary, Oxford, UK.

出版信息

Clin Neuropathol. 1987 Sep-Oct;6(5):185-200.

PMID:3319331
Abstract

Some of the pathological features of 112 cerebellar astrocytomas seen at The Radcliffe Infirmary between 1938 and 1984 have been described. These include the following: Macroscopic appearance: Cerebellar astrocytomas, when compared to other gliomas, have an unusual tendency to become cystic. Thus, if all ages are considered only 22% are total solid tumors while the others have either a large solitary cyst or many smaller ones. Although patients with cystic tumors remain free of recurrence far longer than those with totally solid astrocytomas, the proportion of cystic and solid elements does not significantly influence the overall survival period. Moreover, the degree of tumor demarcation is not an absolute indicator of the degree of malignancy. Extent of disease: Approximately 8% of cerebellar astrocytomas infiltrate the brainstem and these cases are associated with the poorest prognosis. Supratentorial invasion is very rare and CSF dissemination is very uncommon. Only one example of the latter was recorded in the present study. It is important to note that subarachnoid spread may also occur from histologically benign tumors as well as malignant cerebellar astrocytomas. Classification by growth pattern: The classification of cerebellar astrocytomas by "growth pattern" is clearly of limited use. This is due to the presence of substantial transitional forms in both the "juvenile" and "diffuse" as well as in the "fibrillary" and "protoplasmic" classifications. Confusion also arises because of the disregard for the quantity and distribution of certain features which, in turn, limits the usefulness of the "A" and "B" type classification system. Failure to define rigorously the cell type which predominates in the "cerebral" and "diffuse" forms also creates substantial difficulties in using Ringertz' nomenclature. Further problems are caused by Zülich's "polar spongioblastomas" since cerebellar astrocytomas are not composed of primitive spongioblasts, the "polar spongioblastomas" merely representing one subtype of cerebellar astrocytoma, namely the piloid or pilocytic variety. Attempts to classify cerebellar astrocytomas in a manner which does not rely upon any specific cell type but which depends instead upon the degree of homogeneity or heterogeneity of cell growth is of limited value. Grading schemes: Although the tumors studied in the present report were not graded, previous authors have shown that "grading schemes" are of little predictive value in assessing the behavior of cerebellar astrocytomas.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本文描述了1938年至1984年间在拉德克利夫医院所见的112例小脑星形细胞瘤的一些病理特征。具体如下:宏观外观:与其他胶质瘤相比,小脑星形细胞瘤有形成囊肿的异常倾向。因此,若考虑所有年龄段,仅有22%为完全实性肿瘤,其他肿瘤则有一个大的孤立囊肿或多个较小囊肿。尽管囊性肿瘤患者的无复发期远比完全实性星形细胞瘤患者长,但囊性和实性成分的比例对总生存期并无显著影响。此外,肿瘤的分界程度并非恶性程度的绝对指标。疾病范围:约8%的小脑星形细胞瘤浸润脑干,这些病例预后最差。幕上侵犯非常罕见,脑脊液播散也很不常见。本研究仅记录到1例后者情况。需要注意的是,蛛网膜下腔播散也可能发生于组织学上良性的肿瘤以及恶性小脑星形细胞瘤。按生长方式分类:按“生长方式”对小脑星形细胞瘤进行分类显然用处有限。这是因为在“青少年型”和“弥漫型”以及“纤维型”和“原浆型”分类中都存在大量过渡形式。由于忽视某些特征的数量和分布,也会产生混淆,这反过来又限制了“A”型和“B”型分类系统的用处。未能严格定义在“大脑型”和“弥漫型”中占主导的细胞类型,在使用林格茨命名法时也造成了很大困难。祖利希的“极性成胶质细胞瘤”引发了更多问题,因为小脑星形细胞瘤并非由原始成胶质细胞构成,“极性成胶质细胞瘤”仅仅代表小脑星形细胞瘤的一种亚型,即毛细胞型或毛细胞性亚型。试图以不依赖任何特定细胞类型、而是取决于细胞生长的同质或异质程度的方式对小脑星形细胞瘤进行分类,价值有限。分级方案:尽管本报告中研究的肿瘤未进行分级,但先前的作者表明,“分级方案”在评估小脑星形细胞瘤的行为方面预测价值不大。(摘要截断于400字)

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