心脏血管肉瘤的多模态成像

R. Beigel, J. Tress, Louise Jane Thomson, D. Luthringer, A. Shturman, A. Trento, R. Siegel
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引用次数: 0

摘要

心脏原发恶性肿瘤很少见,而血管肉瘤是最常见的心脏恶性肿瘤。病例介绍:我们描述了一个23岁的女性谁提出了一个右心房肿块,这被发现是一个心脏血管肉瘤。我们展示了几种无创成像方式的使用,以及病理证实对心脏血管肉瘤的明确和全面诊断,这是一种罕见的实体。结论:随着无创影像技术的日益普及,血管肉瘤的诊断可以在早期阶段进行。如果血管肉瘤不及时治疗,其预后非常差。治疗选择包括手术切除,化疗,放射治疗,心脏移植或这些组合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodality imaging of a cardiac angiosarcoma
Introduction: While primary malignant tumors of the heart are rare, angiosarcomas are the most common cardiac malignant tumors. Case Presentation: We describe a 23-year-old woman who presented with a right atrial mass, which was discovered to be a cardiac angiosarcoma. We demonstrate the use of several noninvasive imaging modalities along with pathology confirmation for the definitive and comprehensive diagnosis of a cardiac angiosarcoma, a rare entity by itself. Conclusions: With the increasing availability of noninvasive imaging techniques, the diagnosis of angiosarcomas can be made at earlier stages. If angiosarcomas are left untreated, their prognosis is very poor. Therapeutic options include surgical excision, chemotherapy, radiation therapy, and heart transplantation or a combination of these.
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