A Case of Primary Right Atrial Angiosarcoma

Yasuhito Nakamura, Y. Kumada, Y. Mizuno
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Abstract

A Case of Primary Right Atrial Angiosarcoma Yasuhito Nakamura, Yositaka Kumada and Yuusuke Mizuno(Department of Cardiovascular Surgery, Matunami General Hospital, Kasamatu, Japan) Primary cardiac angiosarcoma is extremely rare and its prognosis remains poor. We present a 61-yearold woman with angiosarcoma who was admitted with exertional dyspnea and considerable hemodynamic compromise. Computed tomography showed a large tumor in the right atrium and multiple liver metastases. The cardiac tumor invaded from the superior vena cava to the atrial septum. After the cardiac tumor was removed, the right atrium, the atrial septum and the superior vena cava were reconstructed with a bovine pericardial patch. The pathological diagnosis was angiosarcoma, and the cut-end was positive for sarcoma. The patient survived 14 months after surgery with the aid of adjuvant chemotherapy. Jpn. J. Cardiovasc. Surg. 47 : 45-48(2018)
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原发性右心房血管肉瘤1例
中村康仁、熊田Yositaka、水野佑介(日本笠松町松上总医院心血管外科)原发性心房血管肉瘤极为罕见,预后较差。我们报告一位61岁的女性血管肉瘤患者,她因用力呼吸困难和相当大的血流动力学损害而入院。计算机断层扫描显示右心房有一个大肿瘤和多个肝转移灶。心脏肿瘤从上腔静脉侵入心房间隔。贲门肿瘤切除后,用牛心包补片重建右心房、房间隔和上腔静脉。病理诊断为血管肉瘤,切端为肉瘤阳性。在辅助化疗的帮助下,患者术后存活了14个月。日本。j . Cardiovasc。外科杂志。47:45-48(2018)
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