Tsaprazlis Theoklitos, Stavrakakis Konstantinos E, Kaldis Foivos I, Kostakis Georgios, Filippou Dimitrios
School of Dentistry, National and Kapodistrian University of Athens, Athens, GRC.
Evgenidio Hospital, National and Kapodistrian University of Athens, Athens, GRC.
Cureus. 2025 Mar 12;17(3):e80477. doi: 10.7759/cureus.80477. eCollection 2025 Mar.
Adamantinoma-like Ewing sarcoma (ALES) is a rare malignant neoplasm, identified as a type of Ewing sarcoma (ES), characterized by the EWSR1::FLI1 translocation and a complex immunoprofile. Its various clinical, histopathological, and immunohistochemical features, along with a multitude of diseases in the differential diagnosis, make it a complex entity that requires special attention. Treatment involves parotidectomy alone or in combination with adjuvant chemoradiotherapy. A systematic electronic search was conducted through February 2025 in the PubMed and Scopus databases utilizing relevant Medical Subject Headings, without any time constraints. A total of 35 publications were identified using the keywords "adamantinoma-like Ewing sarcoma" AND "parotid". Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, a total of 15 articles were included in this systematic review, all of which were case reports. Based on the limited information available, it appears that this tumor frequently demonstrates regression after treatment. However, given the small number of recorded cases, a clear survival rate associated with specific therapies remains uncertain. This highlights the importance of ongoing assessments and follow-ups to establish definitive outcomes for patients.
釉质瘤样尤因肉瘤(ALES)是一种罕见的恶性肿瘤,被确定为尤因肉瘤(ES)的一种类型,其特征为EWSR1::FLI1易位和复杂的免疫表型。它具有多种临床、组织病理学和免疫组化特征,以及鉴别诊断中的多种疾病,使其成为一个需要特别关注的复杂实体。治疗方法包括单独腮腺切除术或联合辅助放化疗。截至2025年2月,利用相关医学主题词在PubMed和Scopus数据库中进行了无时间限制的系统电子检索。使用关键词“釉质瘤样尤因肉瘤”和“腮腺”共识别出35篇出版物。按照系统评价和Meta分析的首选报告项目(PRISMA)指南,本系统评价共纳入15篇文章,均为病例报告。根据现有有限信息,该肿瘤似乎在治疗后常出现消退。然而,鉴于记录的病例数量较少,与特定治疗相关的明确生存率仍不确定。这凸显了持续评估和随访以确定患者确切预后的重要性。