Provenzano Sylvio Carvalho, Con Richard, Jones Owen D, Grant Peter W
Department of Cardiothoracic Surgery, Royal Perth Hospital, Wellington Street, Perth, WA 6000, Australia.
Heart Lung Circ. 2006 Aug;15(4):278-9. doi: 10.1016/j.hlc.2006.01.009. Epub 2006 Apr 4.
We report a case of synovial sarcoma of the heart in a 14-year-old boy, who presented with signs of mild generalized illness and rapidly progressed to haemodynamic collapse. On operation the tumour was attached to the tricuspid valve, away from the atrioventricular node. He was considered to have incomplete resection due to extensive adhesions to the atrioventricular junction, and was offered chemotherapy. On 18 months follow-up, he was asymptomatic.
我们报告一例14岁男孩的心脏滑膜肉瘤病例,该男孩最初表现为轻度全身不适症状,随后迅速发展为血流动力学衰竭。手术时肿瘤附着于三尖瓣,远离房室结。由于与房室交界处广泛粘连,被认为切除不完全,遂接受化疗。随访18个月时,他无症状。