Ajmal Namra, Gargano Stacey M, Gosavi Ujwala, Tuluc Madalina
Department of Pathology and Genomic Medicine Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA.
Int J Genomics. 2024 Aug 14;2024:4937501. doi: 10.1155/2024/4937501. eCollection 2024.
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.
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。