携带新型 THBS1::ALK 融合基因的喉复发性炎性肌纤维母细胞瘤

Namra Ajmal, Stacey M. Gargano, Ujwala Gosavi, Madalina Tuluc
{"title":"携带新型 THBS1::ALK 融合基因的喉复发性炎性肌纤维母细胞瘤","authors":"Namra Ajmal,&nbsp;Stacey M. Gargano,&nbsp;Ujwala Gosavi,&nbsp;Madalina Tuluc","doi":"10.1155/2024/4937501","DOIUrl":null,"url":null,"abstract":"<p>Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue tumor primarily occurring in the abdominopelvic region of young patients, and it is characterized by spindle-shaped myofibroblasts, or fibroblasts surrounded by inflammatory infiltrate. Herein, we report a case of a 24-year-old male with a firm submucosal mass in the anterior right vocal fold diagnosed as an IMT that recurred 14 months later. The tumor demonstrated a novel THBS1::ALK fusion containing Exons 1–7 of the thrombospondin 1 (<i>THBS1</i>) gene fused to Exon 19 of the anaplastic lymphoma kinase (<i>ALK</i>) gene via next-generation sequencing with the NextSeq sequencer. The fusion of <i>THBS1</i> to <i>ALK</i> potentially results in increased expression and constitutive activation of the ALK kinase domain. These findings not only broaden the repertoire of known <i>ALK</i> fusion partners implicated in tumorigenesis but also provide a novel avenue for investigating the etiology of recurrent IMT by considering this fusion event as a causal factor. To our knowledge, this is the second case of IMT of the larynx with this novel mutation reported in the literature and the first such case with a detailed description of this specific fusion and clinical recurrence.</p>","PeriodicalId":55239,"journal":{"name":"Comparative and Functional Genomics","volume":"2024 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/2024/4937501","citationCount":"0","resultStr":"{\"title\":\"Recurrent Inflammatory Myofibroblastic Tumor of Larynx Harboring a Novel THBS1::ALK Fusion\",\"authors\":\"Namra Ajmal,&nbsp;Stacey M. Gargano,&nbsp;Ujwala Gosavi,&nbsp;Madalina Tuluc\",\"doi\":\"10.1155/2024/4937501\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue tumor primarily occurring in the abdominopelvic region of young patients, and it is characterized by spindle-shaped myofibroblasts, or fibroblasts surrounded by inflammatory infiltrate. Herein, we report a case of a 24-year-old male with a firm submucosal mass in the anterior right vocal fold diagnosed as an IMT that recurred 14 months later. The tumor demonstrated a novel THBS1::ALK fusion containing Exons 1–7 of the thrombospondin 1 (<i>THBS1</i>) gene fused to Exon 19 of the anaplastic lymphoma kinase (<i>ALK</i>) gene via next-generation sequencing with the NextSeq sequencer. The fusion of <i>THBS1</i> to <i>ALK</i> potentially results in increased expression and constitutive activation of the ALK kinase domain. These findings not only broaden the repertoire of known <i>ALK</i> fusion partners implicated in tumorigenesis but also provide a novel avenue for investigating the etiology of recurrent IMT by considering this fusion event as a causal factor. To our knowledge, this is the second case of IMT of the larynx with this novel mutation reported in the literature and the first such case with a detailed description of this specific fusion and clinical recurrence.</p>\",\"PeriodicalId\":55239,\"journal\":{\"name\":\"Comparative and Functional Genomics\",\"volume\":\"2024 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1155/2024/4937501\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative and Functional Genomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1155/2024/4937501\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative and Functional Genomics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/2024/4937501","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

炎性肌成纤维细胞瘤(IMT)是一种罕见的软组织肿瘤,主要发生在年轻患者的腹盆腔,其特征是纺锤形的肌成纤维细胞或成纤维细胞被炎性浸润所包围。在此,我们报告了一例 24 岁男性患者的病例,他的右声带前部粘膜下肿块质地坚硬,被诊断为内生性声带肿瘤,14 个月后复发。通过使用 NextSeq 测序仪进行下一代测序,该肿瘤显示出一种新型 THBS1::ALK 融合体,其中包含血栓软蛋白 1 (THBS1) 基因的 1-7 号外显子与无性淋巴瘤激酶 (ALK) 基因的 19 号外显子融合。THBS1与ALK的融合可能会导致ALK激酶域的表达增加和组成性激活。这些发现不仅扩大了与肿瘤发生有关的已知ALK融合伙伴的范围,而且通过将这一融合事件视为致病因素,为研究复发性IMT的病因提供了一条新途径。据我们所知,这是文献中报道的第二例存在这种新型突变的喉内膜癌病例,也是第一例详细描述了这种特殊融合和临床复发的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recurrent Inflammatory Myofibroblastic Tumor of Larynx Harboring a Novel THBS1::ALK Fusion

Recurrent Inflammatory Myofibroblastic Tumor of Larynx Harboring a Novel THBS1::ALK Fusion

Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue tumor primarily occurring in the abdominopelvic region of young patients, and it is characterized by spindle-shaped myofibroblasts, or fibroblasts surrounded by inflammatory infiltrate. Herein, we report a case of a 24-year-old male with a firm submucosal mass in the anterior right vocal fold diagnosed as an IMT that recurred 14 months later. The tumor demonstrated a novel THBS1::ALK fusion containing Exons 1–7 of the thrombospondin 1 (THBS1) gene fused to Exon 19 of the anaplastic lymphoma kinase (ALK) gene via next-generation sequencing with the NextSeq sequencer. The fusion of THBS1 to ALK potentially results in increased expression and constitutive activation of the ALK kinase domain. These findings not only broaden the repertoire of known ALK fusion partners implicated in tumorigenesis but also provide a novel avenue for investigating the etiology of recurrent IMT by considering this fusion event as a causal factor. To our knowledge, this is the second case of IMT of the larynx with this novel mutation reported in the literature and the first such case with a detailed description of this specific fusion and clinical recurrence.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Comparative and Functional Genomics
Comparative and Functional Genomics 生物-生化与分子生物学
自引率
0.00%
发文量
0
审稿时长
2 months
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信