Primary Sclerosing Epithelioid Fibrosarcoma of the Kidney: A Case Report and Review of the Literature

IF 0.1 Q4 PATHOLOGY
Mercedes Bravo-Taxa, Rafael Garatea-Grau, Ulises Nuñez-Romero, Lourdes Huanca-Amesquita
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引用次数: 0

Abstract

Abstract Sclerosing epithelioid fibrosarcoma (SEF) is a rare fibrosarcoma variant that features rounded carcinoma-like epithelioid cells arranged into compact nests, cords, and single-cell patterns within a highly sclerotic stroma and has a consistent translocation (EWSR1-CREB3L1/2). To our knowledge, there are 110 cases of pure SEF reported, to date, with 15 occurring at intra-abdominal sites. Primary SEF of the kidney is exceptionally rare. We present a case of SEF that arose in the kidney. Histological examination revealed densely hyalinized epithelioid tumor suggestive of SEF. The diffuse immunohistochemical staining of MUC4 by neoplastic cells and the presence of EWSR1 gene rearrangement by fluorescence in situ hybridization analysis confirmed the histological diagnosis.
原发性肾硬化上皮样纤维肉瘤1例报告及文献复习
硬化性上皮样纤维肉瘤(SEF)是一种罕见的纤维肉瘤变体,其特征是在高度硬化的基质中,圆形癌样上皮样细胞排列成致密的巢状、索状和单细胞模式,并具有一致的易位(EWSR1-CREB3L1/2)。据我们所知,迄今为止有110例纯SEF报告,其中15例发生在腹腔内。原发性肾脏SEF极为罕见。我们报告一例发生在肾脏的SEF。组织学检查显示密集透明化上皮样肿瘤,提示SEF。肿瘤细胞对MUC4进行弥漫性免疫组化染色,荧光原位杂交分析发现EWSR1基因重排,证实了组织学诊断。
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CiteScore
0.30
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