Department of Cardiac Surgery, People's Hospital of Dongyang, Dongyang, Zhejiang, China.
J Card Surg. 2021 Sep;36(9):3452-3455. doi: 10.1111/jocs.15751. Epub 2021 Jul 3.
Cardiac angiosarcoma is a rare but highly malignant cardiac tumor. It is characterized by poor prognosis, and current treatment approaches are not effective.
A 37-year-old female with 35 weeks pregnancy experienced chest tightness and shortness of breath for 1 month. She was diagnosed with primary cardiac angiosarcoma. Delivery of fetus was performed early to treat the mother. The patient underwent resection of the tumor then she was treated with chemotherapy. However, the tumor recurred 11 months after surgery.
Angiosarcoma is a highly malignant tumor explaining recurrence of the tumor recurred after surgery. Cardiac angiosarcoma should be treated through a comprehensive treatment plan, comprising surgery, radiotherapy, and chemotherapy approaches.
心脏血管肉瘤是一种罕见但高度恶性的心脏肿瘤。其预后不良,目前的治疗方法并不有效。
一名 37 岁女性,妊娠 35 周,胸闷、气促 1 个月。诊断为原发性心脏血管肉瘤。为治疗母亲,行胎儿早期分娩。患者行肿瘤切除术,然后接受化疗。但术后 11 个月肿瘤复发。
血管肉瘤是一种高度恶性肿瘤,解释了术后肿瘤复发的原因。心脏血管肉瘤应通过手术、放疗和化疗相结合的综合治疗方案进行治疗。