Department of Anatomic Pathology, Cleveland Clinic, Cleveland, Ohio.
Bone Tumor Reference Center at the Institute for Medical Genetics and Pathology, University Hospital and University of Basel, Basel, Switzerland.
Mod Pathol. 2023 Nov;36(11):100301. doi: 10.1016/j.modpat.2023.100301. Epub 2023 Aug 9.
Adamantinoma-like Ewing sarcoma (ALES) has traditionally been considered a variant of Ewing sarcoma because it generally harbors EWSR1::FLI1 fusions despite showing diffuse positivity for keratins and p40. However, it has become increasingly recognized that different tumors can have identical translocations, including shared fusions between carcinomas and sarcomas, raising questions as to whether ALES might represent a separate entity. Using methylation profiling, we further explored the relationship between Ewing sarcoma and ALES. The archives of multiple institutions were searched for candidate cases of ALES. DNA methylation profiling was performed and results were compared to corresponding data from conventional Ewing sarcoma. Twelve cases of ALES (5 previously reported) were identified in 10 men and 2 women (aged 20-72 years; median age, 41.5 years). Cases included tumors arising in the parotid gland (3), sinonasal cavity (2), submandibular gland (2), thyroid gland (1), neck (1), gingiva (1), hypopharynx (1), and mandible (1). Histologic review consistently showed sheets and nests of basaloid cells within a fibromyxoid or hyalinized stroma. All tumors were positive for at least 1 keratin and CD99 expression, whereas all 10 cases tested were positive for p63 or p40; S100 protein expression was noted in 2 cases. Cases harbored either EWSR1::FLI1 fusions (n = 6), FUS::FLI1 fusions (n = 1), and/or EWSR1 rearrangements (n = 6). Methylation profiling was successful in 11/12 cases evaluated. Unsupervised clustering and dimensionality reduction (Uniform Manifold Approximation and Projection) of DNA methylation data revealed a distinct methylation cluster for all 11 cases, including the tumor with the FUS::FLI1 fusion, which clearly segregated them from the conventional Ewing sarcoma. Follow-up (n = 11, 1-154 months) revealed that 4 patients experienced recurrence and 6 developed metastatic disease. ALES demonstrates a distinct methylation signature from conventional Ewing sarcoma. This finding adds to the distinctive immunoprofile of ALES, suggesting that these 2 tumors should be considered distinct entities rather than histologic extremes of the same disease.
类似于骨外尤文肉瘤的癌肉瘤(ALES)通常表现为角蛋白和 p40 弥漫阳性,但其具有 EWSR1::FLI1 融合,因此传统上被认为是尤文肉瘤的一种变体。然而,人们越来越认识到,不同的肿瘤可能具有相同的易位,包括癌和肉瘤之间的共享融合,这引发了一个问题,即 ALES 是否可能代表一个单独的实体。本研究使用甲基化谱分析进一步探讨了尤文肉瘤和 ALES 之间的关系。在多个机构的档案中搜索 ALES 的候选病例。进行 DNA 甲基化谱分析,并将结果与常规尤文肉瘤的相应数据进行比较。在 10 名男性和 2 名女性(年龄 20-72 岁;中位年龄 41.5 岁)中鉴定出 12 例 ALES(5 例既往报道)。病例包括发生在腮腺(3 例)、鼻腔鼻窦(2 例)、下颌下腺(2 例)、甲状腺(1 例)、颈部(1 例)、牙龈(1 例)、下咽(1 例)和下颌骨(1 例)的肿瘤。组织学复习一致显示在纤维粘液样或玻璃样基质中存在基底细胞的片层和巢。所有肿瘤均至少对 1 种角蛋白和 CD99 表达阳性,而 10 例测试的病例均对 p63 或 p40 阳性;2 例可见 S100 蛋白表达。病例均存在 EWSR1::FLI1 融合(n=6)、FUS::FLI1 融合(n=1)和/或 EWSR1 重排(n=6)。对 12 例评估的病例中的 11 例进行了甲基化谱分析。未监督聚类和 DNA 甲基化数据的维度降低(一致流形逼近和投影)显示,所有 11 例肿瘤均存在独特的甲基化簇,包括具有 FUS::FLI1 融合的肿瘤,这使其与常规尤文肉瘤明显分离。随访(n=11,1-154 个月)显示,4 例患者复发,6 例发生转移疾病。ALES 表现出与常规尤文肉瘤明显不同的甲基化特征。这一发现增加了 ALES 独特的免疫表型,提示这两种肿瘤应被视为不同的实体,而不是同一疾病的组织学极端情况。