Tiraboschi R, Terzi A, Merlo M, Procopio A
Unità Operativa di Cardiochirurgia, Azienda Ospedaliera Ospedali Riuniti, Bergamo.
Ital Heart J Suppl. 2000 Jun;1(6):797-802.
Left atrial myxomas are the most common benign intracardiac tumors. The aim of this study was to compare our experience with the data reported in the literature.
Between May 1985 and August 1999, 26 patients (8 males, 18 females) with left atrial myxomas underwent surgical resection of these tumors at the Department of Cardiac Surgery, Ospedali Riuniti of Bergamo (Italy). Symptoms included congestive heart failure, dyspnea, arrhythmias, chest pain and syncope. Diagnosis was established preoperatively in all patients by echocardiography and angiocardiography was performed in 8 cases. All tumors were excised with a wide margin of uninvolved atrial septum. Two patients underwent concomitant coronary artery bypass.
There was 1 early death due to irreversible ventricular fibrillation. Follow-up was completed for the 25 late survivals. Three patients died, years after operation, due to extracardiac causes. One patients had recurrence of the tumor, which was successfully removed 4 years after initial operation. All other patients are asymptomatic and free from disease.
Operation for left atrial myxoma can be undertaken solely on the basis of echocardiographic findings, but coronary angiography should be performed in older patients who are at risk for coronary artery disease. Surgical excision of left atrial myxomas must be performed as soon as possible after diagnosis is established because of the high risk of valvular obstruction or systemic embolization. Biatrial approach allows for the inspection of the four cardiac chambers, limits manipulation of the mass, and facilitates the complete excision of the tumor. Thus, surgical intervention can be curative for patients with left atrial myxomas and most of these can expect an excellent outcome. Since late recurrence, although rare, has been reported, especially in familial myxomas, long-term clinical and echocardiographic follow-up is recommended.
左心房黏液瘤是最常见的心脏内良性肿瘤。本研究的目的是将我们的经验与文献报道的数据进行比较。
1985年5月至1999年8月期间,26例左心房黏液瘤患者(8例男性,18例女性)在意大利贝加莫联合医院心脏外科接受了这些肿瘤的手术切除。症状包括充血性心力衰竭、呼吸困难、心律失常、胸痛和晕厥。所有患者术前均通过超声心动图确诊,8例患者进行了心血管造影。所有肿瘤均在未累及的房间隔处广泛切除。2例患者同时进行了冠状动脉搭桥术。
1例患者因不可逆的心室颤动早期死亡。对25例晚期存活者完成了随访。3例患者术后数年因心外原因死亡。1例患者肿瘤复发,在初次手术后4年成功切除。所有其他患者均无症状且无疾病。
左心房黏液瘤的手术可仅根据超声心动图检查结果进行,但对于有冠状动脉疾病风险的老年患者应进行冠状动脉造影。由于存在瓣膜阻塞或全身栓塞的高风险,左心房黏液瘤一旦确诊应尽快进行手术切除。双心房入路可检查四个心腔,限制对肿块的操作,并有助于肿瘤的完整切除。因此,手术干预对左心房黏液瘤患者可能具有治愈性,大多数患者可预期良好的预后。由于已报道有晚期复发情况,尽管罕见,尤其是在家族性黏液瘤中,建议进行长期的临床和超声心动图随访。