细胞遗传学和FISH在脑膜瘤诊断中的作用。对189个肿瘤的研究。

Annales de genetique Pub Date : 1998-01-01
H Zattara-Cannoni, D Gambarelli, H Dufour, D Figarella, F Vollot, F Grisoli, A M Vagner-Capodano
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引用次数: 0

摘要

对189例脑膜瘤的细胞遗传学和组织病理学结果进行了分析。肿瘤按分化程度分级。我们在1级(良性)肿瘤中观察到正常核型或只有22个单体,而在3级(间变性)肿瘤中只有1.5%的核型是正常的。2级(非典型)和3级(间变性)肿瘤表现为复杂的结构异常。14号染色体的缺失只发生在3年级。在复杂结构重排的情况下,荧光原位杂交技术(FISH)已经实现,并允许最好的识别异常。在我们的研究中,有5例患者复发。他们表现出染色体异常。复发性脑膜瘤的这些复杂核型可能表明肿瘤的侵袭性特征。我们的研究结果表明,组织病理学和细胞遗传学相关性可能代表脑膜瘤的预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contribution of cytogenetics and FISH in the diagnosis of meningiomas. A study of 189 tumors.

The correlation between cytogenetic and histopathological findings were analysed in 189 meningiomas. The tumors were classified according to increasing degrees of anaplasia. We observed normal karyotype or only monosomy 22 in grade 1 (benign) tumors, while in grade 3 (anaplastic) only 1.5% of karyotypes were normal. Grade 2 (atypical) and 3 (anaplastic) tumors showed complex structural abnormalities. Loss of chromosome 14 were only found in grade 3. In cases with complex structural rearrangements, fluorescence in situ hybridization technique (FISH) has been realized and permitted a best identification of abnormalities. In our series, five patients recurred. They presented chromosomal abnormalities. These complex karyotypes in recurrent meningiomas might indicate aggressive tumor characteristics. Our results indicate histolopathological and cytogenetics correlations might represent a prognostic factor in meningiomas.

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