PLAG1-Rearranged Fibromyxoid and Lipomatous Neoplasms in Children and Adults: Separate Entities or a Morphological Spectrum?

IF 2.8 2区 医学 Q2 GENETICS & HEREDITY
Vanghelita Andrei, Elena Zheleznyakova, Silvia Cavalchini, Jane Chalker, Michael Hubank, Roberto Tirabosco, Paul O'Donnell, Fernanda Amary, Adrienne M. Flanagan
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Abstract

Fusions involving the PLAG1 gene are associated with multiple cancers and benign tumors, including lipoblastoma and the more recently described pediatric fibromyxoid soft tissue tumor. We report two PLAG1-rearranged mesenchymal tumors arising in adults which, although largely similar histologically to the fibromyxoid tumors reported in infants, display limited adipocytic differentiation. In both cases, the novel fusion partner was DLEU2. Whole genome sequencing of one of the tumors also showed loss of 13p including the RB1 locus. Expression of PLAG1 was demonstrated by extensive immunoreactivity in both cases. We discuss the similarities of our cases to the previously described fibroblastic variants of lipoblastomas and the recently reported cases of PLAG1-rearranged fibromyxoid soft tissue tumors, highlighting the overlapping morphological and molecular features. We consider that there is growing evidence that these histological entities are related to conventional lipoblastoma and represent tumors of adipocytic lineage exhibiting different stages of cellular maturation.

Abstract Image

儿童和成人的plag1重排纤维黏液样瘤和脂肪瘤:单独的实体还是形态谱?
涉及PLAG1基因的融合与多种癌症和良性肿瘤有关,包括脂肪母细胞瘤和最近报道的儿童纤维黏液样软组织肿瘤。我们报道了两例发生于成人的plag1重排间充质肿瘤,尽管在组织学上与婴儿中报道的纤维黏液样肿瘤非常相似,但显示出有限的脂肪细胞分化。在这两种情况下,新的核聚变伙伴都是DLEU2。其中一个肿瘤的全基因组测序也显示13p缺失,包括RB1位点。PLAG1在两例患者中均有广泛的免疫反应性表达。我们讨论了我们的病例与先前描述的成纤维细胞变异体脂肪母细胞瘤和最近报道的plag1重排纤维黏液样软组织肿瘤的相似之处,强调了重叠的形态学和分子特征。我们认为,越来越多的证据表明,这些组织学实体与传统的脂肪母细胞瘤有关,并代表脂肪细胞谱系的肿瘤,表现出不同的细胞成熟阶段。
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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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