[伴有1p19q编码缺失的星形细胞瘤]。

Q4 Medicine
M V Ryzhova, S A Galstyan, L V Shishkina, T N Panina, E I Voronina, E N Telysheva, A O Kotelnikova, D V Starovoitov, E G Shaikhaev, G P Snigireva, R V Sycheva, Sh U Kadyrov, A R Adaev, D I Pitskhelauri, E S Kudieva, O G Zheludkova, A V Golanov
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引用次数: 0

摘要

以10年随访的复发性肿瘤为例,作者表明,星形细胞瘤中IDH1/2基因的突变并不总是胶质瘤发病的早期事件,在罕见的情况下,星形细胞瘤中可以发现1p19q密码缺失,并且idh突变肿瘤可能发生在儿童时期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Astrocytoma with 1p19q codeletion].

Using the example of a recurrent tumor with a 10-year follow-up, the authors show that mutation of the IDH1/2 genes in astrocytomas is not always an early event in the pathogenesis of glioma, that in rare cases a 1p19q codeletion can be found in astrocytomas, and that IDH-mutant tumors can occur in childhood.

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来源期刊
Arkhiv patologii
Arkhiv patologii Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
55
期刊介绍: The journal deals with original investigations on pressing problems of general pathology and pathologic anatomy, newest research methods, major issues of the theory and practice as well as problems of experimental, comparative and geographic pathology. To inform readers latest achievements of Russian and foreign medicine the journal regularly publishes editorial and survey articles, reviews of the most interesting Russian and foreign books on pathologic anatomy, new data on modern methods of investigation (histochemistry, electron microscopy, autoradiography, etc.), about problems of teaching, articles on the history of pathological anatomy development both in Russia and abroad.
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