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上颌骨梭形细胞肉瘤:一种罕见病例、病例报告及文献综述

Spindle Cell Sarcoma of the Maxilla: A Rare Entity, Case Report, and Review of the Literature.

作者信息

Mahajan Sumeet, Chavan Purushottam, Dandagi Satyajit, Suma M N, Greeshma P

机构信息

MCH Resident, Kidwai Memorial Institute of Oncology, Bangalore, India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2024 Oct;76(5):4813-4817. doi: 10.1007/s12070-024-04870-x. Epub 2024 Jul 13.

Abstract

Spindle cell sarcoma (SCS) is a malignancy, with the most recent Surveillance, Epidemiology, and End Results (SEER) data citing a total of 250 reported cases occurring in the head and neck. Of these cases, none originated in the maxillofacial hard tissue. The diagnosis of SCS requires its differentiation from other sarcomas and spindle cell neoplasms. Therefore, a comprehensive review to reinforce its inclusion in oral and maxillofacial surgeons' differential diagnosis for osseous neoplastic pathology is desired. In the present case report, we have described a recurrent case of Maxillary Undifferentiated Spindle cell sarcoma in a 11 year old male child post chemoradiotherapy which was excised intoto successfully .

摘要

梭形细胞肉瘤(SCS)是一种恶性肿瘤,最新的监测、流行病学和最终结果(SEER)数据显示,头颈部共报告了250例病例。在这些病例中,没有一例起源于颌面硬组织。SCS的诊断需要将其与其他肉瘤和梭形细胞瘤进行鉴别。因此,需要进行全面综述,以加强其在口腔颌面外科医生对骨肿瘤病理学鉴别诊断中的纳入。在本病例报告中,我们描述了一名11岁男性儿童在放化疗后复发性上颌未分化梭形细胞肉瘤的病例,该病例已成功完整切除。

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本文引用的文献

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Margin Analysis: Sarcoma of the Head and Neck.边缘分析:头颈部肉瘤
Oral Maxillofac Surg Clin North Am. 2017 Aug;29(3):355-366. doi: 10.1016/j.coms.2017.04.002.
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Oral Spindle Cell Sarcoma: A Rare Case Report and Review of Literature.口腔梭形细胞肉瘤:1例罕见病例报告及文献复习
J Clin Diagn Res. 2017 Apr;11(4):ZD23-ZD25. doi: 10.7860/JCDR/2017/24592.9699. Epub 2017 Apr 1.
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Head and neck sarcomas: analysis of the SEER database.头颈部肉瘤:监测、流行病学与最终结果(SEER)数据库分析
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