Denız Hayati, Koruk Senem, Kırbas Ahmet, Atık Cem, Ozcalıskan Ozerdem, Ustunsoy Hasim
Department of Cardio-Vascular Surgery, Gaziantep University Medical Faculty, Gaziantep, Turkey.
Heart Surg Forum. 2011 Apr;14(2):E133-4. doi: 10.1532/HSF98.20091177.
Cardiac leiomyosarcoma is a rare tumor with poor survival prospects. Surgery prolongs survival, but the tumor often recurs early after surgery. The diagnosis is often made by transthoracic echocardiography. Magnetic resonance imaging and computed tomography are required to characterize the location and extent of cardiac masses. In this report, we present a patient with a leiomyosarcoma that was resected completely. The tumor was located in the left atrium, mimicked a myxoma, and protruded into the left ventricle during diastole.
心脏平滑肌肉瘤是一种罕见的肿瘤,生存前景不佳。手术可延长生存期,但肿瘤常在术后早期复发。诊断通常通过经胸超声心动图进行。需要磁共振成像和计算机断层扫描来确定心脏肿块的位置和范围。在本报告中,我们介绍了一名平滑肌肉瘤患者,其肿瘤已被完全切除。肿瘤位于左心房,类似黏液瘤,在舒张期突入左心室。