Zhou Xiang, Song Laichun, Liu Hongyan, Cheng Youping, Han Xiao
Department of Cardiac Surgery, Wuhan Asia Heart Hospital, Wuhan, China.
Department of Pathology, Wuhan Asia General Hospital, Wuhan, China.
J Card Surg. 2022 Nov;37(11):3878-3879. doi: 10.1111/jocs.16862. Epub 2022 Aug 18.
Primary cardiac alveolar rhabdomyosarcoma (ARMS) is an extremely rare malignant tumor with dismal prognosis. We herein report a case of right atrial ARMS in a 63-year-old female with intermittent dizziness. Complete surgical resection of the mass was performed and the postoperative histopathologic examination confirmed ARMS. The patient received adjuvant therapy after surgery and was doing well at 1-year follow-up.
原发性心脏肺泡横纹肌肉瘤(ARMS)是一种极其罕见的恶性肿瘤,预后很差。我们在此报告一例63岁患有间歇性头晕的女性右心房ARMS病例。对肿块进行了完整的手术切除,术后组织病理学检查确诊为ARMS。患者术后接受了辅助治疗,在1年随访时情况良好。