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一位 73 岁男性,既往有创伤史,此次因偶然诊断出三角肌内黏液瘤。

A 73-Year-Old Man with an Incidental Diagnosis of Deltoid Intramuscular Myxoma Following a History of Trauma.

机构信息

Department of Medicine, Reading Hospital, Tower Health System, West Reading, PA, USA.

Department of Pathology, Reading Hospital, Tower Health System, West Reading, PA, USA.

出版信息

Am J Case Rep. 2022 Aug 8;23:e936654. doi: 10.12659/AJCR.936654.

DOI:10.12659/AJCR.936654
PMID:35934869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9373044/
Abstract

BACKGROUND Intramuscular myxomas are rare and benign soft-tissue tumors of uncertain differentiation. Predisposing or precipitating factors have not yet been reported. Activating mutation in GNAS (exons 8 and 9) is detected in >90% of sporadic cases. The role of chronic myopathy, tendinopathy, or trauma to muscles in the etiology of these neoplasms is not known. We report an unusual case of a deltoid mass found following longstanding rotator cuff tendinopathy and a recent fall, later confirmed to be an intramuscular myxoma on biopsy. CASE REPORT A 73-year-old man with a 5-year history of left shoulder pain and rotator cuff tear presented with intractable pain in his left shoulder after a recent fall at home. Physical examination was suggestive of a rotator cuff injury and magnetic resonance imaging (MRI) of the left shoulder revealed a 2.7×2.5×3.7cm T1 hypo- and T2 hyperintense oblong mass-like signal abnormality with heterogeneous, predominantly peripheral enhancement within the deltoid muscle concerning for a malignant mass. Surgical resection was carried out along with left reverse total shoulder replacement, and histopathology revealed findings consistent with an intramuscular myxoma. CONCLUSIONS Intramuscular myxomas are rare, benign tumors. This case report presents one such myxoma incidentally found in a patient with longstanding rotator cuff tendinopathy and a recent fall. Although this co-occurrence is likely incidental, further research and case series review of similar presentations may influence postulations of the pathophysiology of myxomas.

摘要

背景

肌内黏液瘤是一种罕见的、分化不确定的良性软组织肿瘤。目前尚未报道其发病的诱发或促成因素。>90%的散发性病例中可检测到 GNAS(外显子 8 和 9)的激活突变。这些肿瘤的病因与慢性肌病、肌腱病或肌肉创伤的关系尚不清楚。我们报告了一例不常见的三角肌肿块病例,该病例在长期肩袖肌腱病和近期跌倒后发现,经活检证实为肌内黏液瘤。

病例报告

一名 73 岁男性,有 5 年左肩部疼痛和肩袖撕裂病史,近期在家中跌倒后出现左肩部顽固性疼痛。体格检查提示肩袖损伤,左肩关节磁共振成像(MRI)显示三角肌内有一个 2.7×2.5×3.7cm 的 T1 低信号和 T2 高信号的椭圆形肿块样信号异常,伴不均匀、主要为外周强化,考虑恶性肿块。进行了手术切除和左反向全肩关节置换术,组织病理学显示符合肌内黏液瘤的发现。

结论

肌内黏液瘤是罕见的良性肿瘤。本病例报告介绍了一例在长期肩袖肌腱病和近期跌倒的患者中偶然发现的肌内黏液瘤。尽管这种同时发生可能是偶然的,但对类似表现的进一步研究和病例系列回顾可能会影响对黏液瘤发病机制的推测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/58b40ef2d455/amjcaserep-23-e936654-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/c126670b1c60/amjcaserep-23-e936654-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/045006cb527a/amjcaserep-23-e936654-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/8df8b68471c4/amjcaserep-23-e936654-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/46896d9cbebb/amjcaserep-23-e936654-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/58b40ef2d455/amjcaserep-23-e936654-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/c126670b1c60/amjcaserep-23-e936654-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/045006cb527a/amjcaserep-23-e936654-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/8df8b68471c4/amjcaserep-23-e936654-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/46896d9cbebb/amjcaserep-23-e936654-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/9373044/58b40ef2d455/amjcaserep-23-e936654-g005.jpg

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本文引用的文献

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Diagnostic value of ultrasonography and other imaging examinations in patients with intramuscular myxoma: A case series and literature review.超声检查及其他影像学检查对肌内黏液瘤患者的诊断价值:病例系列研究与文献综述
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检测肌内/细胞性黏液瘤中的GNAS突变作为黏液样软组织肿瘤分类的诊断工具。
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A case of intramuscular myxoma presenting as a swollen shoulder: a case report.一例表现为肩部肿胀的肌内黏液瘤:病例报告
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