Department of Medical Genetics, Tohoku University School of Medicine, Sendai, 980-8574, Japan.
Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
J Hum Genet. 2020 Nov;65(11):995-1001. doi: 10.1038/s10038-020-0794-y. Epub 2020 Jun 26.
Gorham-Stout disease (GSD), a rare disorder of unknown etiology, is characterized by massive osteolysis that is associated with proliferation and dilation of lymphatic vessels. Variants in cancer-associated genes have been described in complex lymphatic anomalies. To explore the pathogenesis of GSD, we performed the amplicon-based deep sequencing on 50 cancer-related genes to assay affected tissues from the six patients with GSD. In one patient, a somatic activating KRAS c.182A > G variant (p.Q61R) was detected in 1% of the tissue sample. Conversely, the mutant allele was not detected in uninvolved normal skin and blood samples. Histopathology of the patient's tissue sample showed proliferation of abnormal lymphatic and blood vascular endothelial cells, osteoclasts, and activated macrophages. The activating KRAS variant is a known 'hotspot' variant, frequently identified in several types of human cancer. This is the first report of identifying a pathogenic variant in a patient with GSD. This finding may set the stage for elucidation of pathophysiology and the development of novel therapies for GSD.
戈勒姆-斯托特病(GSD)是一种病因不明的罕见疾病,其特征为骨质溶解,伴有淋巴管的增殖和扩张。在复杂的淋巴异常中已经描述了与癌症相关基因的变异。为了探索 GSD 的发病机制,我们对 50 个与癌症相关的基因进行了基于扩增子的深度测序,以检测来自 6 名 GSD 患者的受累组织。在一名患者中,在 1%的组织样本中检测到了体细胞激活的 KRAS c.182A>G 变异(p.Q61R)。相反,未受累的正常皮肤和血液样本中未检测到突变等位基因。患者组织样本的组织病理学显示异常淋巴管和血管内皮细胞、破骨细胞和活化的巨噬细胞增殖。激活的 KRAS 变异是一个已知的“热点”变异,经常在几种人类癌症中被发现。这是首例在 GSD 患者中发现致病性变异的报告。这一发现可能为阐明 GSD 的病理生理学和开发新的治疗方法奠定基础。