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Combined myoepithelial carcinoma and myoepithelioma in soft tissue: a case report and review of the literature

机译:软组织中合并肌上皮癌和肌上皮瘤的病例报告及文献复习

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Introduction Soft tissue myoepithelial carcinoma and myoepithelioma are rare entities, part of myoepithelial tumors. They were incorporated into the World Health Organization classification of soft tissue tumors in 2002. Here we present an exceptional case of myoepithelial carcinoma and myoepithelioma association. To the best of our knowledge, such an association has never been reported in the literature. Case presentation We report a case of myoepithelial carcinoma combined with myoepithelioma occurring in the soft tissue of the right forearm of an 84-year-old Arabian man. We describe the clinical, radiological and pathological features dominated by histological polymorphism. We will also describe the proposed histological criteria of malignancy and the major role of immunohistochemistry in positive and differential diagnosis. We finally mention the therapeutic arsenal available. Conclusion Through this work, we report that myoepithelioma of soft tissue can progress to malignant myoepithelioma.
机译:简介软组织肌上皮癌和肌上皮瘤是罕见的实体,是肌上皮肿瘤的一部分。它们于2002年被纳入世界卫生组织软组织肿瘤分类。在这里,我们介绍了肌上皮癌和肌上皮瘤协会的特殊情况。据我们所知,文献中从未报道过这种关联。病例介绍我们报告了一名84岁阿拉伯男子右前臂软组织中发生的肌上皮癌合并肌上皮瘤的病例。我们描述了以组织学多态性为主的临床,放射学和病理学特征。我们还将描述拟议的恶性组织学标准以及免疫组织化学在阳性和鉴别诊断中的主要作用。我们最后提到可用的治疗武库。结论通过这项工作,我们报道软组织肌上皮瘤可以发展为恶性肌上皮瘤。

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