Department of Pathology, Samsung Medical Center, Sungkyunkwan University College of Medicine, Gangnamgu, Seoul, Korea.
Pathol Int. 2012 Jan;62(1):65-8. doi: 10.1111/j.1440-1827.2011.02752.x. Epub 2011 Nov 24.
Sclerosing epithelioid fibrosarcoma (SEF) is a rare but distinct variant of fibrosarcoma. A 43-year-old man presented with a lesion in his back that had been present for three years but had recently increased in size. Magnetic resonance imaging (MRI) revealed a 6-cm sized ovoid mass showing low intensities on T1 and T2 weighted images. Histologically, the tumor was of moderate cellularity, and the cells were relatively uniform in size and shape. The cells were epithelioid, round, oval and polygonal with clear and slightly eosinophilic cytoplasm, forming nests, cords, or sheet-like patterns with a dense collagenous and hyalinized matrix. The tumor was positive for vimentin, but negative for smooth muscle actin, desmin, HMB45, and CD34. Although the tumor showed nuclear overexpression of beta-catenin protein, the CTNNB1 exon3 mutation was not detected. Fluorescent in situ hybridization for FUS using dual color break-apart probes showed rearrangement of the FUS. In accordance with previous studies, our case showed positive findings of FUS rearrangement, reinforcing the notion of a close relationship between low grade fibromyxoid sarcoma and SEF.
硬化性上皮样纤维肉瘤(SEF)是一种罕见但独特的纤维肉瘤变体。一名 43 岁男性因背部病变就诊,该病变已存在三年,但最近病变增大。磁共振成像(MRI)显示一个 6 厘米大小的卵圆形肿块,在 T1 和 T2 加权图像上显示低信号。组织学上,肿瘤细胞中等数量,细胞大小和形状相对均匀。细胞呈上皮样,圆形、椭圆形和多边形,胞浆透明,嗜酸性轻度,形成巢状、条索状或片状结构,伴有致密的胶原和玻璃样基质。肿瘤阳性表达波形蛋白,但阴性表达平滑肌肌动蛋白、结蛋白、HMB45 和 CD34。虽然肿瘤β-连环蛋白蛋白核表达过度,但未检测到 CTNNB1 外显子 3 突变。使用双色分离探针的 FUS 荧光原位杂交显示 FUS 重排。与以往研究一致,我们的病例显示 FUS 重排的阳性发现,进一步证实了低度纤维黏液样肉瘤和 SEF 之间的密切关系。