Maloney Nolan, Bridge Julia A, de Abreu Francine, Korkolopoulou Penelope, Sakellariou Stratigoula, Linos Konstantinos
Department of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center and Geisel School of Medicine at Dartmouth, One Medical Center Drive, New Hampshire, Lebanon.
Department of Pathology and Microbiology, University of Nebraska Medical Center, 983135 Nebraska Medical Center, Omaha, Nebraska 68198-3135, The Translational Genomics Research Institute (TGen), Phoenix, Arizona.
J Cutan Pathol. 2019 Jul;46(7):532-537. doi: 10.1111/cup.13469. Epub 2019 May 3.
Dermatofibrosarcoma protuberans (DFSP) is a translocation-associated, low-grade sarcoma with fibroblastic differentiation. It is the most common superficial sarcoma, almost exclusively arising within the dermis. In a minority of cases, there is a transition from the conventional morphology to a fibrosarcomatous pattern, known as a fibrosarcomatous DFSP (FS-DFSP). Although a number of different molecular alterations have been described to account for this transformation, it remains poorly understood. Herein we report the first case of a FS-DFSP with a fusion between ERG, an ETS family transcription factor, and MAP3K7CL, a kinase gene rarely observed in fusion gene events.
隆突性皮肤纤维肉瘤(DFSP)是一种与易位相关的、具有成纤维细胞分化的低级别肉瘤。它是最常见的浅表性肉瘤,几乎仅起源于真皮层。在少数病例中,会出现从传统形态向纤维肉瘤样模式的转变,即纤维肉瘤样隆突性皮肤纤维肉瘤(FS-DFSP)。尽管已经描述了许多不同的分子改变来解释这种转变,但对此仍知之甚少。在此,我们报告首例具有ERG(一种ETS家族转录因子)与MAP3K7CL(一种在融合基因事件中很少观察到的激酶基因)融合的FS-DFSP病例。