Sakaguchi Masayuki, Minato Naoki, Katayama Yuji, Nakashima Atsushi
Department of Thoracic and Cardiovascular Surgery, Fukuoka Tokusyukai Hospital, Kasuga, Japan.
Ann Thorac Cardiovasc Surg. 2006 Apr;12(2):145-8.
Primary cardiac angiosarcoma is a rare tumor associated with a poor prognosis. We report a case of a 59-year-old woman with right atrial angiosarcoma presenting with cardiac tamponade due to right atrial perforation. She underwent urgent surgical resection of the tumor. However, the patient died 68 days after surgery due to local recurrence. An effective treatment for cardiac angiosarcoma has not yet been established. However, more aggressive treatment with a combination of surgery, radiation, chemotherapy and IL-2 should be considered.
原发性心脏血管肉瘤是一种罕见的肿瘤,预后较差。我们报告一例59岁女性右心房血管肉瘤病例,该患者因右心房穿孔导致心脏压塞。她接受了紧急肿瘤手术切除。然而,患者术后68天因局部复发死亡。目前尚未确立心脏血管肉瘤的有效治疗方法。然而,应考虑采用手术、放疗、化疗和白细胞介素-2联合的更积极治疗方案。