胸锁乳突肌肌内脂肪瘤:罕见病例再探

IF 1.9 Q3 PATHOLOGY
Clinical Pathology Pub Date : 2024-06-10 eCollection Date: 2024-01-01 DOI:10.1177/2632010X241260200
Jad Hosri, Yara Yammine, Nadine El Hadi, Jessica Aoun, Marc Mourad, Usamah Hadi
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引用次数: 0

摘要

肌内脂肪瘤通常发生在皮下组织,很少影响深层肌肉平面,尤其是头颈部。以下是 3 例涉及胸锁乳突肌的肌肉内脂肪瘤病例。前两名患者表现为无痛、可触及的肿块,经影像诊断证实为环绕性肌内脂肪瘤。其中一名患者接受了手术治疗,另一名患者接受了保守治疗,并进行了监测和密切随访。第三位患者报告吞咽困难,并伴有偶尔的呼吸困难和轻微疼痛。肿块被确定为浸润性脂肪瘤,并进行了手术切除。第一例和最后一例患者的肿瘤完全切除,6 个月后无复发。对第二个病例进行了 3 个月和 6 个月的连续随访,结果没有发生间隔变化。我们报告了胸锁乳突肌肌内脂肪瘤的最大病例系列,以加深我们对这一罕见病例的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intramuscular Lipoma of the Sternocleidomastoid Muscle: A Rare Entity Revisited.

Intramuscular lipomas, typically found in subcutaneous tissue, rarely affect deeper muscular planes, especially those of the head and neck region. The following are 3 cases of intramuscular lipomas involving the sternocleidomastoid muscle. The first 2 patients presented with painless, palpable masses confirmed by diagnostic imaging as well-circumscribed intramuscular lipomas. One was treated surgically, while the other was managed conservatively with monitoring and close follow-up. The third patient reported dysphagia associated with occasional dyspnea and mild pain. The mass was identified as infiltrative lipoma and was resected surgically. Complete tumor removal with no recurrence at 6 months was observed for the first and last cases. The second case was serially followed at 3 and 6 months with no interval changes. We report the largest case series on intramuscular lipomas of the sternocleidomastoid muscle to enhance our understanding of this rare entity.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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