具有异常融合基因CBX6的KMT2A重新排列的肉瘤::KMT2A::PYGO1
Harumi Nakamura1,2, Yoji Kukita3, Toru Wakamatsu4
1Laboratory of Genomic Pathology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka, Osaka, 5418567, Japan. harumi.nakamura@oici.jp.
Virchows Archiv : an international journal of pathology
|September 15, 2023
概括
具有KMT2A基因重组的罕见瘤,通常是侵略性的,可以呈现出新型的融合基因,如CBX6::KMT2A::PYGO1. 这种特定的KMT2A重组导致了一种非复发的螺旋细胞瘤,这表明各种KMT2A融合伙伴影响瘤行为.
科学领域:
- 在瘤学瘤学.
- 遗传学 遗传学 是一个
- 病理学 病理学 病理学
背景情况:
- 在年轻人中,越来越多地报告了具有KMT2A重组的罕见瘤.
- 这些瘤往往表现出一种类似纤维素瘤的硬化表皮质形态和攻击性行为.
- 常见的融合基因包括YAP1::KMT2A::YAP1和VIM::KMT2A.
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