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首页> 外文期刊>Clinical neuropathology >Identification of t(1;19)(q12;p13) and ploidy changes in an ependymosarcoma: a cytogenetic evaluation.
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Identification of t(1;19)(q12;p13) and ploidy changes in an ependymosarcoma: a cytogenetic evaluation.

机译:在室间隔肉瘤中鉴定t(1; 19)(q12; p13)和倍性变化:细胞遗传学评估。

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摘要

Gliosarcoma, a recognized subtype of glioblastoma, is a biphasic tumor exhibiting distinct glial and sarcomatous components. Ependymosarcomas are rarer, biphasic ependymal tumors exhibiting sarcomatous change. Genetic abnormalities associated with this curious phenotype are not well understood. We are presenting the first karyotype of ependymosarcoma with identification of a clonal t(1;19)(q12;p13). Fluorescence in situ hybridization (FISH) was performed with a probe set targeting 1q23 and 19p13.3. Although the tumor did not show evidence of t(1;19)(q23;p13.3) by FISH, increased ploidy was a feature of the sarcomatous component. On clinical followup the patient is doing well without evidence of recurrence 55 months after initial resection, and postoperative treatment with irradiation and temozolomide. The significance of the genetic alterations we describe associated with sarcomatoid change in ependymal neoplasms, and ultimately their prognostic relevance, merits further study.
机译:胶质肉瘤是胶质母细胞瘤的公认亚型,是一种双相性肿瘤,表现出明显的神经胶质和肉瘤成分。室管膜肉瘤是罕见的双相室间隔瘤,表现出肉瘤样变化。与这种奇怪的表型有关的遗传异常尚未得到很好的理解。我们提出了克隆性t(1; 19)(q12; p13)的鉴定的第一个核型室管膜肉瘤。用靶向1q23和19p13.3的探针组进行荧光原位杂交(FISH)。尽管肿瘤未通过FISH显示t(1; 19)(q23; p13.3)的证据,但倍数性却是肉瘤成分的特征。在临床随访中,患者情况良好,没有证据表明初次切除术后55个月以及放疗和替莫唑胺的术后治疗均复发。我们描述的与室管膜肿瘤中肉瘤样变化相关的遗传改变的重要性,以及最终与预后的相关性,值得进一步研究。

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