Leiomyosarcoma in sternocleidomastoid muscle: a case report

José Gabriel Miranda da Paixão, I. Martins, Vinicius Fialho Teixeira
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Abstract

Financial support: None Conflicts of interest: No conflicts of interest declared concerning the publication of this article. Submitted: August 25, 2020. Accepted: October 21, 2020. The study was carried out at Hospital Ophir Loyola, Belém, PA, Brasil. abstract Introduction: Leiomyosarcoma (LMS) is rare, although commonly described in oral cavity. It can appear anywhere smooth muscle is present and there are reports of this type of neoplasm in many subsites in head and neck. Case Report: 44-year-old male patient with 2-year-history of cervical nodule, progressively growing, causing pain and neck movement limitation. Patient underwent en bloc resection of the tumor along with right ECM muscle, cervical levels II, III, IV and V. Discussion: Primary resection with wide margins is the treatment of choice for localized lesions. The present case originating in ECM may be unique until now, but it was handled based on the available literature and presented a satisfactory outcome.
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胸锁乳突肌平滑肌肉瘤1例
资金支持:无利益冲突:与本文发表相关的声明无利益冲突。提交:2020年8月25日。录用日期:2020年10月21日。这项研究是在巴西宾夕法尼亚州belsamim的Ophir Loyola医院进行的。摘要简介:平滑肌肉瘤(LMS)虽常见于口腔,但罕见。它可以出现在任何有平滑肌存在的地方,有报道称这种类型的肿瘤在头颈部的许多亚位。病例报告:44岁男性,2年宫颈结节病史,进行性生长,引起疼痛和颈部活动受限。患者行肿瘤与右ECM肌、宫颈II、III、IV、v节整块切除。讨论:大切缘一期切除是局部病变的治疗选择。本病例起源于ECM可能是独一无二的,直到现在,但它是根据现有的文献处理,并提出了令人满意的结果。
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