Bean Gregory R, Joseph Nancy M, Gill Ryan M, Folpe Andrew L, Horvai Andrew E, Umetsu Sarah E
Department of Pathology, University of California, San Francisco, CA, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Mod Pathol. 2017 May;30(5):722-727. doi: 10.1038/modpathol.2016.234. Epub 2017 Jan 13.
Anastomosing hemangiomas are recently described benign vascular lesions that occur chiefly in the genitourinary tract and paravertebral soft tissues. Owing to their rarity and unusual cytoarchitectural features, anastomosing hemangiomas are frequently confused with low-grade angiosarcomas. The specific genetic alterations underlying these lesions are currently unknown. We performed capture-based next-generation DNA sequencing analysis on 13 anastomosing hemangiomas and identified frequent somatic mutations in the heterotrimeric G-protein alpha-subunit, GNAQ. Nine of 13 cases (69%) harbored a somatic mutation at GNAQ codon 209, a known hotspot that is commonly mutated in uveal melanoma and blue nevi, as well as various congenital vascular proliferations. No other pathogenic or likely pathogenic mutations were identified in these genetically simple lesions. The finding of a recurrent driver mutation in the G-protein signal transduction pathway provides strong evidence that anastomosing hemangiomas are indeed clonal vascular neoplasms.
吻合性血管瘤是最近才被描述的良性血管病变,主要发生于泌尿生殖道和椎旁软组织。由于其罕见性和不寻常的细胞结构特征,吻合性血管瘤常被误诊为低级别血管肉瘤。目前尚不清楚这些病变潜在的具体基因改变。我们对13例吻合性血管瘤进行了基于捕获的二代DNA测序分析,发现异源三聚体G蛋白α亚基GNAQ存在频繁的体细胞突变。13例中有9例(69%)在GNAQ密码子209处发生体细胞突变,该位点是已知的热点突变位点,在葡萄膜黑色素瘤、蓝色痣以及各种先天性血管增殖性病变中常见。在这些基因结构简单的病变中未发现其他致病或可能致病的突变。G蛋白信号转导通路中反复出现驱动突变这一发现有力地证明了吻合性血管瘤确实是克隆性血管肿瘤。