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本文引用的文献

1
Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendothelioma.通过靶向 RNA 测序诊断已知肉瘤融合基因和新型融合伙伴,并在假肌源性血管内皮瘤中鉴定出一种反复出现的 ACTB-FOSB 融合。
Mod Pathol. 2019 May;32(5):609-620. doi: 10.1038/s41379-018-0175-7. Epub 2018 Nov 21.
2
BRAF V600E Mutations Occur in a Subset of Glomus Tumors, and Are Associated With Malignant Histologic Characteristics.BRAF V600E突变存在于一小部分血管球瘤中,并与恶性组织学特征相关。
Am J Surg Pathol. 2017 Nov;41(11):1532-1541. doi: 10.1097/PAS.0000000000000913.
3
Myopericytomatosis: Clinicopathologic Analysis of 11 Cases With Molecular Identification of Recurrent PDGFRB Alterations in Myopericytomatosis and Myopericytoma.肌周细胞瘤病:11例临床病理分析及肌周细胞瘤病和肌周细胞瘤中复发性血小板衍生生长因子受体B(PDGFRB)改变的分子鉴定
Am J Surg Pathol. 2017 Aug;41(8):1034-1044. doi: 10.1097/PAS.0000000000000862.
4
BRAF V600E is not a consistent feature of myopericytoma.BRAF V600E并非肌周细胞瘤的一致特征。
J Cutan Pathol. 2016 Dec;43(12):1248-1249. doi: 10.1111/cup.12832.
5
Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and Myopericytomas.散发性婴儿/孤立性成人肌纤维瘤中存在复发性体细胞PDGFRB突变,而血管平滑肌瘤和肌周细胞瘤中则不存在。
Am J Surg Pathol. 2017 Feb;41(2):195-203. doi: 10.1097/PAS.0000000000000752.
6
Role of BRAFV600E in the first preclinical model of multifocal infiltrating myopericytoma development and microenvironment.BRAFV600E在多灶性浸润性肌周细胞瘤发生及微环境首个临床前模型中的作用
J Natl Cancer Inst. 2014 Jul 25;106(8). doi: 10.1093/jnci/dju182. Print 2014 Aug.
7
Novel MIR143-NOTCH fusions in benign and malignant glomus tumors.良性和恶性血管球瘤中的新型 MIR143-NOTCH 融合。
Genes Chromosomes Cancer. 2013 Nov;52(11):1075-87. doi: 10.1002/gcc.22102. Epub 2013 Sep 2.
8
Somatic uniparental isodisomy explains multifocality of glomuvenous malformations.体单亲源同二倍体解释了丛状静脉畸形的多灶性。
Am J Hum Genet. 2013 Feb 7;92(2):188-96. doi: 10.1016/j.ajhg.2012.12.017. Epub 2013 Jan 31.
9
BRAF and KRAS mutations in sporadic glomus tumors.散发性血管球瘤中的BRAF和KRAS突变
Am J Dermatopathol. 2012 Jul;34(5):533-5. doi: 10.1097/DAD.0b013e31823931b4.
10
Gastrointestinal glomus tumors: a clinicopathologic, immunohistochemical, and molecular genetic study of 32 cases.胃肠道血管球瘤:32例临床病理、免疫组织化学及分子遗传学研究
Am J Surg Pathol. 2002 Mar;26(3):301-11. doi: 10.1097/00000478-200203000-00003.

血管球瘤和相关的周细胞肿瘤的分子再评价——强调 NOTCH 基因融合。

A Molecular Reappraisal of Glomus Tumors and Related Pericytic Neoplasms With Emphasis on NOTCH-gene Fusions.

机构信息

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.

Department of Pathology & Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada.

出版信息

Am J Surg Pathol. 2020 Nov;44(11):1556-1562. doi: 10.1097/PAS.0000000000001531.

DOI:10.1097/PAS.0000000000001531
PMID:32604167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7554116/
Abstract

Glomus tumors (GTs), together with myofibroma (MF), myopericytoma (MP), and angioleiomyoma (AL) are classified as members of the perivascular myoid family of tumors. The reported genetic abnormalities across these neoplasms is dissimilar, arguing against a pathogenetically unified family; half of the GT showing NOTCH-gene fusions and a smaller subset BRAF V600E mutations, while PDGFRB mutations are noted in a subset of MF and MP. This study aimed to investigate the prevalence and specificity of NOTCH-gene fusions in a large group of GT and correlate with clinical features. BRAF-VE1 and PDGFRB immunoexpression was also investigated in this cohort. A total of 93 GT and 43 other pericytic lesions (11 MP, 13 MF, and 19 AL) were selected. All cases were tested by fluorescence in situ hybridization for NOTCH1-4 and MIR143 gene abnormalities and 6 cases were investigated by targeted RNA-sequencing. Fluorescence in situ hybridization revealed NOTCH-gene rearrangements in 50 (54%) GT, 2 MP (18%), and 2 AL (11%). NOTCH-rearrangements were present in 34 (68%) benign and 16 (32%) malignant GT. Fusion-positive benign GT were overwhelmingly seen in males with a predilection for extremities, while the malignant GT occurred mostly in viscera. Among the fusion-negative GT, 88% were benign, 9% uncertain malignant potential, and 2% malignant. Half of the fusion-negative GTs occurred in the finger/subungual region. In summary, rearrangements of NOTCH genes are seen in over half of GT, with NOTCH2-MIR143 being the most common fusion (73%), while only a small subset of AL and MP share these abnormalities. The common subungual GT subset lack NOTCH-gene fusions suggesting an alternative pathogenesis. BRAF-VE1 was negative in all 37 cases studied, while strong PDGFRB staining was seen in 14 (21%) cases. Additional studies are needed to investigate the genetic alterations in the fusion-negative cases.

摘要

血管周肌细胞肿瘤(GTs)与肌纤维瘤(MF)、肌周细胞瘤(MP)和血管平滑肌脂肪瘤(AL)一起被归类为血管周肌源性肿瘤家族的成员。这些肿瘤的报道遗传异常不同,这表明它们不是一个具有共同发病机制的家族;一半的 GT 显示 NOTCH 基因融合,一小部分具有 BRAF V600E 突变,而 PDGFRB 突变则见于一部分 MF 和 MP。本研究旨在调查一组大型 GT 中 NOTCH 基因融合的流行率和特异性,并与临床特征相关联。本研究还对这组肿瘤的 BRAF-VE1 和 PDGFRB 免疫表达进行了研究。共选择了 93 例 GT 和 43 例其他血管周细胞病变(11 例 MP、13 例 MF 和 19 例 AL)。所有病例均通过荧光原位杂交技术检测 NOTCH1-4 和 MIR143 基因异常,其中 6 例通过靶向 RNA 测序进行检测。荧光原位杂交显示 50 例(54%)GT、2 例 MP(18%)和 2 例 AL(11%)存在 NOTCH 基因重排。NOTCH 重排在 34 例(68%)良性和 16 例(32%)恶性 GT 中存在。融合阳性的良性 GT 主要见于男性,且好发于四肢,而恶性 GT 则主要发生在内脏。在融合阴性的 GT 中,88%为良性,9%为恶性潜能不确定,2%为恶性。融合阴性 GT 的一半发生在手指/甲下区域。总之,超过一半的 GT 存在 NOTCH 基因重排,NOTCH2-MIR143 是最常见的融合(73%),而只有一小部分 AL 和 MP 存在这些异常。常见的甲下 GT 亚组缺乏 NOTCH 基因融合,提示其发病机制可能不同。在研究的 37 例中,BRAF-VE1 均为阴性,而 14 例(21%)存在强烈的 PDGFRB 染色。需要进一步研究以探讨融合阴性病例的遗传改变。