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原发性心脏肿瘤:右心房血管肉瘤1例报告并文献复习

Primary cardiac tumor: a case report of right atrial angiosarcoma and review of the literature.

作者信息

Guo Yujian, Liu Qianzhen, Wu Haibo

机构信息

Department of Changzhi People's Hospital, The Affiliated Hospital of Changzhi Medical College, Changzhi, Shanxi, China.

Department of Pathology, The First People's Hospital of Foshan, Foshan, Guangdong, China.

出版信息

Front Oncol. 2023 May 26;13:1164153. doi: 10.3389/fonc.2023.1164153. eCollection 2023.

Abstract

Primary cardiac angiosarcoma is a relatively rare tumor with early metastasis and poor prognosis. Radical resection of the primary tumor remains the primary approach for the optimal survival of patients with early-stage cardiac angiosarcoma without evidence of metastasis. This case involves a 76-year-old man with symptoms of chest tightness, fatigue, pericardial effusion, and arrhythmias who achieved good results after surgery to treat the angiosarcoma in the right atrium. In addition, literature analysis showed that surgery remains an effective way of treating primary early angiosarcoma.

摘要

原发性心脏血管肉瘤是一种相对罕见的肿瘤,早期易发生转移,预后较差。对于无转移证据的早期心脏血管肉瘤患者,根治性切除原发性肿瘤仍然是实现最佳生存的主要方法。该病例为一名76岁男性,有胸闷、乏力、心包积液和心律失常症状,其右心房血管肉瘤手术后取得了良好效果。此外,文献分析表明,手术仍然是治疗原发性早期血管肉瘤的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4016/10250602/e88e51cc1b78/fonc-13-1164153-g001.jpg

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