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Atypical Intramuscular Myxoma of the Lumbosacral Paraspinal Muscle: The First Case Report in Asian

机译:腰ac椎旁肌的非典型肌内粘液瘤:亚洲第一例病例报告

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摘要

Intramuscular myxoma (IM) is a benign neoplasm of mesenchymal origin. We report a rare case of IM which was located in the lumbosacral paraspinal muscles. A 62-year-old female patient presented with progressive low back pain for 2 months, and the radiologic findings showed a large mass (4.0×3.5×6.5 cm) in the right lumbosacral paraspinal area. Total resection of the tumor was performed and the symptom was nearly resolved after surgery. Although the immuno-histopathological analysis was consistent with IM, there were some different findings from typical pathological characteristics of IM in this case. Firstly, the symptomatic change of the mass took relatively short time (less than 3 months), and this change was accompanied by partial calcification inside the mass. Moreover, iatrogenic interruption of paravertebral muscle by the other previous operation might be the promoting factor of the fibrous dysplasia, which can explain the pathogenesis of IM. To our knowledge, this is the eighth case of the lumbar paraspinal myxoma reported in the literatures and the first case in Asian population.
机译:肌内粘液瘤(IM)是间充质起源的良性肿瘤。我们报告的一种罕见的IM病例位于腰s椎旁肌。一名62岁的女性患者出现了2个月的进行性腰背痛,影像学检查结果显示右侧腰s脊柱旁区域肿物较大(4.0×3.5×6.5 cm)。进行了肿瘤的全切除,手术后症状几乎消失了。尽管免疫组织病理学分析与IM一致,但在这种情况下,IM的典型病理特征有一些不同的发现。首先,肿块的症状变化需要相对较短的时间(少于3个月),并且此变化伴有肿块内部的部分钙化。此外,医源性椎旁肌的其他先前手术中断可能是纤维异常增生的促进因素,这可以解释IM的发病机理。据我们所知,这是文献报道的第八例腰椎旁粘液瘤,也是亚洲人群中的第一例。

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