原发性心脏黏液样脂肪肉瘤伪装成大量心包积液1例

Bhargavi Ilangovan, A. S., Archana Lakshmanan, Jeganniwas Kannan
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引用次数: 0

摘要

心脏肿瘤非常罕见,而且大多是良性的。肉瘤在心脏中极为罕见。黏液样脂肪肉瘤主要起源于心脏和心包膜,也可能是其他部位的转移性疾病。患者表现为心包积液对压力的影响。超声心动图、心脏MRI和活检通常可以确诊。手术是治疗这种肿瘤的唯一选择,但由于肿瘤的位置和出现时的晚期性质,手术很少可行。我们报道这一病例是因为其罕见,并强调需要多机构研究以改善结果。关键词:黏液样脂肪肉瘤;手术;心脏流体;大量心包积液
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Primary Myxoid Liposarcoma of the Heart Masquerading as Massive Pericardial Effusion
Tumors of the heart are very rare and are mostly benign. Sarcomas are extremely rare in the heart. Myxoid Liposarcomas can arise primarily from the heart and the pericardium or can be metastatic disease from elsewhere. The patients present with pericardial effusion of pressure effects. Echocardiography, cardiac MRI and biopsy usually clinches the diagnosis. Surgery is the only curative option for this tumor and is seldom possible due to the location and advanced nature at presentation. We are reporting this case due to its rarity and to emphasize the need for multi-institutional studies to improve the outcomes. Keywords: Myxoid liposarcoma; Surgery; Cardiac fluid; Massive Pericardial Effusion
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