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65例人类脑膜瘤细胞遗传学与组织病理学结果的相关性

Correlation between cytogenetic and histopathological findings in 65 human meningiomas.

作者信息

Casalone R, Simi P, Granata P, Minelli E, Giudici A, Butti G, Solero C L

机构信息

Biologia Generale e Genetica Medica, Università di Pavia, Italy.

出版信息

Cancer Genet Cytogenet. 1990 Apr;45(2):237-43. doi: 10.1016/0165-4608(90)90088-r.

Abstract

The correlations between cytogenetic and histopathological findings were analyzed in 65 cases of human meningiomas. Clonal chromosome abnormalities were present in 28 cases (43%). The overall female/male ratio was 1.7, but it was 1.1 in the group of 28 cases with chromosomal abnormalities. Abnormalities of chromosome 22 as sole abnormality predominate in the female patients. The mean age of patients with normal karyotype was significantly lower (50.7 years) than that of patients with chromosome changes (57.3 years). The tumor origin was predominantly at the base in the patients with normal karyotype but different at the convexity, falx cerebri, and spinal cord. The five abnormal cases from the spinal cord all showed involvement of chromosome 22. The proportion of chromosome anomalies was different in the various histological types, and a significant difference was found between the meningotheliomatous (23%) and psammomatous (58%) types. The cytogenetically abnormal cases of the psammomatous type all showed involvement of chromosome 22. In three patients with multiple meningiomas, we found different karyotypes in the different tumors of the same patient, which may indicate a multifocal origin of the tumors.

摘要

对65例人脑膜瘤的细胞遗传学和组织病理学结果之间的相关性进行了分析。28例(43%)存在克隆性染色体异常。总体男女比例为1.7,但在28例染色体异常的病例组中为1.1。仅22号染色体异常在女性患者中占主导。核型正常患者的平均年龄(50.7岁)显著低于有染色体改变的患者(57.3岁)。核型正常患者的肿瘤主要起源于颅底,但在凸面、大脑镰和脊髓处则不同。来自脊髓的5例异常病例均显示22号染色体受累。不同组织学类型中染色体异常的比例不同,在脑膜瘤型(23%)和砂粒体型(58%)之间发现了显著差异。砂粒体型细胞遗传学异常病例均显示22号染色体受累。在3例多发性脑膜瘤患者中,我们在同一患者的不同肿瘤中发现了不同的核型,这可能表明肿瘤起源于多灶性。

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