Suppr超能文献

一名伴有嗜酸性粒细胞增多及酪氨酸激酶基因融合(ETV6::LYN融合基因)的髓系/淋系肿瘤患者的全外显子组测序分析

Whole exome sequencing analysis of a patient with myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions with ETV6::LYN fusion gene.

作者信息

Hosoba Rika, Fukuhara Suguru, Kogure Yasunori, Takano Kosuke, Shibata Maki, Horiuchi Toshikatsu, Kobayashi Shinichi, Makita Shinichi, Iwaki Noriko, Munakata Wataru, Maeshima Akiko Miyagi, Kimura Fumihiko, Kataoka Keisuke, Izutsu Koji

机构信息

Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.

Division of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.

出版信息

Ann Hematol. 2025 Jan;104(1):809-813. doi: 10.1007/s00277-024-06135-7. Epub 2024 Dec 20.

Abstract

ETV6::LYN fusion gene is recognized as one of the genetic alterations responsible for myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions (MLN-TK) according to the 2022 WHO classification. However, the clinical features and pathogenesis of MLN-TK with ETV6::LYN are not well defined because of the rarity of the disease. Here, we report an MLN-TK patient with ETV6::LYN that manifested as myeloproliferative neoplasms (MPN) with eosinophilia, myelofibrosis, and T-lymphoblastic lymphoma (T-LBL), which eventually led to acute myeloid leukemia. Targeted RNA sequencing of both lymph node specimens diagnosed with T-LBL and bone marrow specimens diagnosed with MPN specimens detected an identical ETV6::LYN fusion gene. Whole exome sequencing (WES) detected several identical missense and nonsense mutations in both specimens. Detected mutations were not found to be relevant to pathogenesis of T-LBL and MPN in previous reports and were considered variants of uncertain significance. Based on the WES results, ETV6::LYN fusion gene was considered the driver gene essential for the pathogenesis of MPN-TK with ETV6::LYN.

摘要

根据2022年世界卫生组织分类,ETV6::LYN融合基因被认为是导致伴有嗜酸性粒细胞增多和酪氨酸激酶基因融合的髓系/淋系肿瘤(MLN-TK)的基因改变之一。然而,由于该疾病罕见,伴有ETV6::LYN的MLN-TK的临床特征和发病机制尚未明确。在此,我们报告1例伴有ETV6::LYN的MLN-TK患者,其表现为伴有嗜酸性粒细胞增多的骨髓增殖性肿瘤(MPN)、骨髓纤维化和T淋巴细胞母细胞淋巴瘤(T-LBL),最终发展为急性髓系白血病。对诊断为T-LBL的淋巴结标本和诊断为MPN的骨髓标本进行靶向RNA测序,检测到相同的ETV6::LYN融合基因。全外显子测序(WES)在两个标本中检测到几个相同的错义突变和无义突变。在既往报告中未发现检测到的突变与T-LBL和MPN的发病机制相关,被认为是意义未明的变异。基于WES结果,ETV6::LYN融合基因被认为是伴有ETV6::LYN的MPN-TK发病机制中的驱动基因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验