血管肿瘤中的 CIC::DUX4 融合基因病例扩展了 CIC 重组肉瘤的范围。

IF 1.6 4区 医学 Q3 DERMATOLOGY Journal of Cutaneous Pathology Pub Date : 2024-07-15 DOI:10.1111/cup.14682
William R. Jeck, Sarah Rapisardo, Barbara A. Anderson, Peter Hendrickson, George Jour, Richard F. Riedel, Brian E. Brigman, Rami N. Al-Rohil
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引用次数: 0

摘要

CIC重组肉瘤是一组侵袭性极强的圆形细胞肉瘤。这些肿瘤最常见的表现是CIC::DUX4融合,组织病理学表现与尤文肉瘤相似,但最近也出现了模仿血管肿瘤的病变。在此,我们描述了一例通过基于 RNA 的分子检测发现的 CIC::DUX4 融合肉瘤患者,该患者最初被诊断为内皮肿瘤。肿瘤表现为广泛的血管形态生长,WT1完全阴性,免疫组化显示ERG、CD31和DUX4的染色呈全局阳性。肿瘤的甲基化检测结果显示,血管肉瘤比 CIC 重排肉瘤更接近血管肉瘤。我们的研究结果表明,CIC::DUX4 融合瘤的表型范围可能比以前认识到的更多样化,并提供了证据表明,准确诊断需要同时进行分子和免疫组化研究。
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Case of a CIC::DUX4 fusion gene in a vascular neoplasm extends the spectrum of CIC-rearranged sarcomas

CIC-rearranged sarcomas comprise a group of exceptionally aggressive round-cell sarcomas. These tumors most commonly demonstrate CIC::DUX4 fusion and show similar histopathology to Ewing sarcomas, though lesions mimicking vascular neoplasms have recently been described. Here, we describe a case of a patient with CIC::DUX4 fusion sarcoma identified using RNA-based molecular testing who was initially diagnosed with an endothelial neoplasm. The tumor showed extensive vasoformative growth, complete WT1 negativity, and global positive staining for ERG, CD31, and DUX4 by immunohistochemistry. Methylation testing of the tumor clustered more closely with angiosarcomas than with CIC-rearranged sarcomas. Our findings suggest that CIC::DUX4 fused neoplasms may demonstrate a more diverse phenotypic range than previously appreciated and offer evidence that both molecular and immunohistochemical studies are needed for accurate diagnosis.

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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
174
审稿时长
3-8 weeks
期刊介绍: Journal of Cutaneous Pathology publishes manuscripts broadly relevant to diseases of the skin and mucosae, with the aims of advancing scientific knowledge regarding dermatopathology and enhancing the communication between clinical practitioners and research scientists. Original scientific manuscripts on diagnostic and experimental cutaneous pathology are especially desirable. Timely, pertinent review articles also will be given high priority. Manuscripts based on light, fluorescence, and electron microscopy, histochemistry, immunology, molecular biology, and genetics, as well as allied sciences, are all welcome, provided their principal focus is on cutaneous pathology. Publication time will be kept as short as possible, ensuring that articles will be quickly available to all interested in this speciality.
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