Furukawa Nobuyuki, Gummert Jan, Börgermann Jochen
Department of Cardiothoracic Surgery, Heart and Diabetes Center North Rhine-Westphalia, Georgstr. 11, 32545, Bad Oeynhausen, Germany.
J Cardiothorac Surg. 2012 Sep 27;7:96. doi: 10.1186/1749-8090-7-96.
Primary cardiac tumors are rare with an incidence ranging from 0.001% to 0.03% in autopsy series. The prognosis of cardiac sarcomas remains poor because it proliferates rapidly and distant metastases are often found at diagnosis. A 47-year-old male complained of persistent cough. The chest roentgenogram was normal. Subsequent computed tomography revealed a mass in the right atrium. Echocardiography and magnetic resonance imaging confirmed also a right atrial mass (34 x 35 mm) infiltrating the atrial septum. The tumor was completely resected en bloc, including the anterior and lateral right atrial walls, the left atrial dome, and a large segment of the superior vena cava, and reconstructed the atria and superior vena cava with bovine pericardium. The tumor was histologically and immunohistochemically diagnosed as undifferentiated pleomorphic sarcoma. This type of cardiac sarcoma is very rare and usually found in the left atrium. Twenty-seven months after surgery, the patient is doing well without metastasis or local tumor recurrence.
原发性心脏肿瘤很罕见,在尸检系列中的发病率为0.001%至0.03%。心脏肉瘤的预后仍然很差,因为它增殖迅速,且在诊断时常常发现有远处转移。一名47岁男性主诉持续咳嗽。胸部X线片正常。随后的计算机断层扫描显示右心房有一个肿块。超声心动图和磁共振成像也证实了右心房有一个肿块(34×35毫米),侵犯了房间隔。肿瘤被完整切除,包括右心房前壁和侧壁、左心房顶部以及上腔静脉的一大段,并用牛心包重建了心房和上腔静脉。肿瘤经组织学和免疫组织化学诊断为未分化多形性肉瘤。这种类型的心脏肉瘤非常罕见,通常发生在左心房。手术后27个月,患者情况良好,无转移或局部肿瘤复发。