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舌骨舌肌肌内黏液瘤:一例报告及文献复习

Intramuscular myxoma of the hyoglossus muscle: A case report and literature review.

作者信息

Li Guiqi, Jiang Wen, Li Wei, Li Junchuan

机构信息

Department of Stomatology, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei 434000, P.R. China.

Department of Pathology, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei 434000, P.R. China.

出版信息

Oncol Lett. 2014 May;7(5):1679-1682. doi: 10.3892/ol.2014.1955. Epub 2014 Mar 7.

DOI:10.3892/ol.2014.1955
PMID:24765200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3997683/
Abstract

Intramuscular myxoma (IM) is a benign intramuscular neoplasm composed of fibroblasts and abundant myxoid stroma. IMs most commonly affect larger skeletal muscles, while those affecting the oral and maxillofacial regions are rare, with a small number of documented cases in the available literature. The aim of the present study was to describe a highly rare case of an IM within the hyoglossus muscle of the tongue in a 74-year-old male. The patient presented with a painless mass in the submental space that had been growing slowly for more than five years. A computed tomography scan revealed a hypodense lesion located in the root of the tongue. The mass was easily excised with thin margins, including only a small amount of the adjacent muscle tissue. The pathological diagnosis of the mass was an IM. The patient made an excellent recovery following the surgery and the follow-up three years later revealed no local recurrence. IMs of the hyoglossus muscle are highly rare, however must be considered in the differential diagnosis of swellings in the root of the tongue region.

摘要

肌内黏液瘤(IM)是一种由成纤维细胞和丰富的黏液样基质组成的良性肌内肿瘤。IM最常累及较大的骨骼肌,而累及口腔颌面部区域的则较为罕见,现有文献中仅有少数病例记载。本研究的目的是描述一例74岁男性舌内舌骨舌肌内高度罕见的IM病例。患者颏下间隙出现无痛性肿块,已缓慢生长五年多。计算机断层扫描显示舌根部有一个低密度病变。肿块很容易被切除,切缘很薄,仅包括少量相邻肌肉组织。肿块的病理诊断为IM。患者术后恢复良好,三年后的随访显示无局部复发。舌骨舌肌的IM非常罕见,但在舌根部肿胀的鉴别诊断中必须予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/c8387c22f09c/OL-07-05-1679-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/f9f4eaa0567d/OL-07-05-1679-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/a8e6d00251bd/OL-07-05-1679-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/c8387c22f09c/OL-07-05-1679-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/f9f4eaa0567d/OL-07-05-1679-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/a8e6d00251bd/OL-07-05-1679-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd39/3997683/c8387c22f09c/OL-07-05-1679-g02.jpg

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本文引用的文献

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Intramuscular myxoma associated with an increased carbohydrate antigen 19.9 level in a woman: a case report.一名女性患者的肌内黏液瘤伴糖类抗原19.9水平升高:病例报告
J Med Case Rep. 2011 May 14;5:184. doi: 10.1186/1752-1947-5-184.
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Intramuscular myxoma of the nasal vestibule.鼻前庭肌内黏液瘤
Auris Nasus Larynx. 2010 Feb;37(1):100-2. doi: 10.1016/j.anl.2009.02.014. Epub 2009 May 2.
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Intramuscular myxoma of the masseter muscle. A case report.咬肌肌内黏液瘤。病例报告。
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Intramuscular myxoma of the paraspinal muscles: A case report and systematic review of the literature.椎旁肌内黏液瘤:一例报告及文献系统综述
Oncol Lett. 2016 Jan;11(1):466-470. doi: 10.3892/ol.2015.3864. Epub 2015 Nov 5.
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Intramuscular myxoma presenting as a rare posterior neck mass in a young child: case report and literature review.小儿罕见的颈部后方肌肉内黏液瘤病例报告及文献复习
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Intramuscular myxoma report of a case diagnosed on fine needle aspiration cytology.细针穿刺细胞学诊断肌内黏液瘤1例报告
Indian J Pathol Microbiol. 2004 Apr;47(2):279-81.
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Intramuscular myxoma of scalene muscle: a case report.斜角肌肌内黏液瘤:一例报告
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Case report: Myxoma of the temporalis muscle.病例报告:颞肌黏液瘤
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INTRAMUSCULAR MYXOMA; A REVIEW AND FOLLOW-UP STUDY OF 34 CASES.肌内黏液瘤:34例病例的回顾与随访研究
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