101例颅底肿瘤细胞遗传学分析。

Head & Neck Pub Date : 2008-05-01 DOI:10.1002/hed.20741
Ziv Gil, Avi Orr-Urtreger, Nadia Voskoboinik, Leonor Trejo-Leider, Ruth Shomrat, Dan M Fliss
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引用次数: 3

摘要

背景:颅底肿瘤是一种罕见的肿瘤,有关这些肿瘤的细胞遗传学资料有限。作者对大量肿瘤进行了细胞遗传学分析,并将结果与患者的病理资料进行了比较。方法:对101例肿瘤切除术患者病理证实标本,采用g带和光谱核型技术进行核型分析。结果:67例恶性肿瘤中,32例(48%)存在染色体畸变,部分存在复杂的数字和结构染色体异常。在鳞状细胞癌、腺样囊性癌(ACCs)、鼻窦未分化癌、脊索瘤和肉瘤中发现了复发性染色体断点。特定的断点建立了各种软组织肉瘤的诊断。在其他各种恶性和良性肿瘤中发现了新的染色体畸变。结论:本研究强调了细胞遗传学分析在颅底肿瘤诊断中的价值。这些数据为这些罕见肿瘤的生物学行为提供了进一步的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytogenetic analysis of 101 skull base tumors.

Background: Skull base tumors are rare neoplasms and the cytogenetic data on these tumors are limited. The authors cytogenetically analyzed a large series of tumors and compared the findings with patients' pathologic data.

Methods: The karyotypes of pathologically confirmed samples of 101 patients, who were operated for oncological extirpation of tumors, were analyzed using G-banding and spectral-karyotyping techniques.

Results: Of the 67 malignant tumors, 32 (48%) had chromosomal aberrations, some with complex numerical and structural chromosomal anomalies. Recurrent chromosomal breakpoints were identified in squamous cell carcinomas, adenoid cystic carcinomas (ACCs), sinonasal undifferentiated carcinomas, chordomas, and sarcomas. Specific breakpoints established the diagnosis of various soft tissue sarcomas. Novel chromosomal aberrations were found in various other malignant and benign tumors.

Conclusion: This study highlights the value of cytogenetic analysis for diagnosis of skull base tumors. The data add further information on the biological behavior of these rare neoplasms.

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