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喉部复发性炎性肌纤维母细胞瘤伴新型THBS1::ALK融合基因

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

作者信息

Ajmal Namra, Gargano Stacey M, Gosavi Ujwala, Tuluc Madalina

机构信息

Department of Pathology and Genomic Medicine Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA.

出版信息

Int J Genomics. 2024 Aug 14;2024:4937501. doi: 10.1155/2024/4937501. eCollection 2024.

DOI:10.1155/2024/4937501
PMID:39171208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11338662/
Abstract

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 () gene fused to Exon 19 of the anaplastic lymphoma kinase () gene via next-generation sequencing with the NextSeq sequencer. The fusion of to potentially results in increased expression and constitutive activation of the ALK kinase domain. These findings not only broaden the repertoire of known 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.

摘要

炎性肌纤维母细胞瘤(IMT)是一种罕见的软组织肿瘤,主要发生于年轻患者的腹盆腔区域,其特征为梭形肌成纤维细胞或被炎性浸润包围的成纤维细胞。在此,我们报告一例24岁男性患者,其右前声带黏膜下有一质地硬的肿物,诊断为IMT,14个月后复发。通过使用NextSeq测序仪进行二代测序,该肿瘤显示出一种新的THBS1::ALK融合,即血小板反应蛋白1(THBS1)基因的第1 - 7外显子与间变性淋巴瘤激酶(ALK)基因的第19外显子融合。THBS1与ALK的融合可能导致ALK激酶结构域的表达增加和组成性激活。这些发现不仅拓宽了与肿瘤发生相关的已知ALK融合伴侣的范围,还通过将这种融合事件视为一个致病因素,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具有这种新突变的喉IMT病例,也是第一例对这种特定融合及临床复发进行详细描述的此类病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/e2b810da676f/IJG2024-4937501.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/7e2b28bcdd9f/IJG2024-4937501.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/e60033555294/IJG2024-4937501.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/e2b810da676f/IJG2024-4937501.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/7e2b28bcdd9f/IJG2024-4937501.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/e60033555294/IJG2024-4937501.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59e4/11338662/e2b810da676f/IJG2024-4937501.003.jpg

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本文引用的文献

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Therapeutic Advances of Rare ALK Fusions in Non-Small Cell Lung Cancer.治疗非小细胞肺癌中罕见 ALK 融合的新进展。
Curr Oncol. 2022 Oct 16;29(10):7816-7831. doi: 10.3390/curroncol29100618.
2
Inflammatory myofibroblastic tumour of the larynx: report of a case.喉炎性肌纤维母细胞瘤:一例报告
Ear Nose Throat J. 2025 Feb;104(2):NP68-NP71. doi: 10.1177/01455613221101087. Epub 2022 May 9.
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Inflammatory myofibroblastic tumor of the larynx: Case report.喉炎性肌纤维母细胞瘤:病例报告
Clin Case Rep. 2021 Sep 15;9(9):e04796. doi: 10.1002/ccr3.4796. eCollection 2021 Sep.
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Inflammatory Myofibroblastic Tumors in Children: A Clinical Retrospective Study on 19 Cases.儿童炎性肌纤维母细胞瘤:19例临床回顾性研究
Front Pediatr. 2021 Jul 8;9:543078. doi: 10.3389/fped.2021.543078. eCollection 2021.
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ALK-negative lung inflammatory myofibroblastic tumor in a young adult: A case report and literature review of molecular alterations.ALK 阴性青年肺炎性肌纤维母细胞瘤:分子改变的病例报告及文献复习。
Medicine (Baltimore). 2021 May 21;100(20):e25972. doi: 10.1097/MD.0000000000025972.
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Clinicopathologic and Genomic Characterization of Inflammatory Myofibroblastic Tumors of the Head and Neck: Highlighting a Novel Fusion and Potential Diagnostic Pitfall.头颈部炎性肌纤维母细胞瘤的临床病理及基因组特征:强调一种新的融合基因及其潜在的诊断陷阱。
Am J Surg Pathol. 2021 Dec 1;45(12):1707-1719. doi: 10.1097/PAS.0000000000001735.
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THBS1 regulates trophoblast fusion through a CD36-dependent inhibition of cAMP, and its upregulation participates in preeclampsia.凝血酶敏感蛋白1通过CD36依赖性抑制环磷酸腺苷来调节滋养层融合,其上调参与子痫前期。
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