一种携带TPM3::ALK融合的皮肤上皮样血管肿瘤。

IF 3.1 2区 医学 Q2 GENETICS & HEREDITY Genes, Chromosomes & Cancer Pub Date : 2023-10-03 DOI:10.1002/gcc.23207
Konstantinos Linos, Jason C. Chang, Klaus J. Busam
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引用次数: 0

摘要

在过去的二十年里,在理解与血管肿瘤相关的分子途径方面取得了实质性进展。除了突变和拷贝数畸变外,融合已成为血管肿瘤一个显著亚群发病机制的重要因素。在本报告中,我们提出了一个不寻常的皮内血管肿瘤上皮样细胞形态。免疫组织化学显示CD31、ERG和因子VIII呈弥漫性阳性,支持其内皮谱系。RNA测序(ArcherFusion Plex)揭示了基因TPM3外显子8和ALK外显子20之间存在框内融合。免疫组织化学证实内皮细胞表达ALK。据我们所知,这是第一个记录在案的携带ALK融合的血管肿瘤病例。它可能属于上皮样血管瘤的范围;然而,我们不能完全排除它本身是一个独特的、潜在的、独特的良性实体的可能性。
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A cutaneous epithelioid vascular tumor harboring a TPM3::ALK fusion

Substantial progress has been made in understanding the molecular pathways associated with vascular tumors over the last two decades. In addition to mutations and copy number aberrations, fusions have emerged as significant contributors to the pathogenesis of a notable subset of vascular tumors. In this report, we present a case of an unusual intradermal vascular tumor with epithelioid cytomorphology. Immunohistochemistry revealed diffuse positivity for CD31, ERG and Factor VIII, supporting its endothelial lineage. RNA sequencing (ArcherFusion Plex) revealed the presence of an in-frame fusion between the genes TPM3 Exon 8 and ALK Exon 20. Immunohistochemistry confirmed ALK expression by the endothelial cells. To our knowledge, this is the first documented case of a vascular tumor harboring an ALK fusion. It may fall within the spectrum of epithelioid hemangiomas; nevertheless, we cannot definitively exclude the possibility of it being a distinct and potentially unique benign entity on its own.

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来源期刊
Genes, Chromosomes & Cancer
Genes, Chromosomes & Cancer 医学-遗传学
CiteScore
7.00
自引率
8.10%
发文量
94
审稿时长
4-8 weeks
期刊介绍: Genes, Chromosomes & Cancer will offer rapid publication of original full-length research articles, perspectives, reviews and letters to the editors on genetic analysis as related to the study of neoplasia. The main scope of the journal is to communicate new insights into the etiology and/or pathogenesis of neoplasia, as well as molecular and cellular findings of relevance for the management of cancer patients. While preference will be given to research utilizing analytical and functional approaches, descriptive studies and case reports will also be welcomed when they offer insights regarding basic biological mechanisms or the clinical management of neoplastic disorders.
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