Intra-osseous sclerosing epithelioid fibrosarcoma of the mandible: A case report and review of the literature

Joshua Allen , Daniel Hovander , Dolphine Oda , Erica Kao , Robert W. Ricciotti
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Abstract

We report a rare case of sclerosing epithelioid fibrosarcoma (SEF) arising in the anterior mandible of a 49-year-old male confirmed by the detection of an EWSR1-CREB3L3 fusion gene. SEF of the oral cavity is rare. To our knowledge this case marks the twelfth reported case to date. Our report and review of the literature highlights the molecular, immunophenotypic, and unique clinicopathological features of SEF in the oral cavity, specifically, its predilection for the jaw bones. Although SEF is usually a malignancy of soft tissue, nine (75%) of the reported oral cavity cases have occurred as a primary jaw neoplasm. The mandible represents the most common location with seven cases, while two occurred in the maxilla. These findings suggest a propensity for bone involvement in the oral cavity, which may be a feature unique to this site.

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下颌骨骨内硬化性上皮样纤维肉瘤1例报告及文献复习
我们报告一例罕见的硬化上皮样纤维肉瘤(SEF),发生在一名49岁男性的前下颌骨,通过检测EWSR1-CREB3L3融合基因确诊。口腔SEF是罕见的。据我们所知,这是迄今为止报告的第12例病例。我们的报告和文献综述强调了口腔SEF的分子、免疫表型和独特的临床病理特征,特别是它对颌骨的偏爱。虽然SEF通常是软组织的恶性肿瘤,但9例(75%)的口腔病例是作为原发性颌骨肿瘤发生的。下颌骨是最常见的位置,7例,而2例发生在上颌骨。这些发现表明口腔有骨受累的倾向,这可能是该部位独有的特征。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
发文量
0
审稿时长
16 weeks
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