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Primary cardiac myxofibrosarcoma with osteoid differentiation mimicking a left atrial myxoma: A rare entity

机译:原发性心脏肌瘤瘤瘤与骨质分化模仿左心肌肌瘤:罕见实体

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摘要

Cardiac myxofibrosarcoma (MFS) is an uncommon entity. It is among the most challenging conditions to diagnose due to its rarity, high variability, and non-specific findings. These tumors often simulate left atrial myxoma or mitral stenosis at clinical presentation. Although, the definitive diagnosis of cardiac tumors depends on histopathological examination, various imaging techniques are also useful to study tumor characteristics to plan an appropriate treatment strategy. Here we highlight a case of primary cardiac MFS of left atrium (LA) showing areas of transition to undifferentiated pleomorphic sarcoma (UPS) with bone or osteoid formation, which is extremely rare and not well described.
机译:心脏肌瘤肌肉瘤(MFS)是一个罕见的实体。由于其罕见,高可变性和非特定调查结果,是诊断的最具挑战性的条件之一。这些肿瘤通常在临床介绍中模拟左心房肌瘤或二尖瓣狭窄。虽然,心脏肿瘤的尾部诊断取决于组织病理学检查,但各种成像技术也可用于研究肿瘤特征以规划适当的治疗策略。在这里,我们突出了左心肌(LA)的原发性心脏MFS的情况,显示到未分化的牙龈肉瘤(UPS)的过渡区域,具有骨骼或骨质形成,这极罕见并未良好地描述。

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