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心脏黏液瘤:49例患者的24年经验

Cardiac myxomas: 24 years of experience in 49 patients.

作者信息

Keeling I M, Oberwalder P, Anelli-Monti M, Schuchlenz H, Demel U, Tilz G P, Rehak P, Rigler B

机构信息

Department of Surgery, Division of Cardiac Surgery, Karl Franzens University Graz, Graz, Austria.

出版信息

Eur J Cardiothorac Surg. 2002 Dec;22(6):971-7. doi: 10.1016/s1010-7940(02)00592-4.

Abstract

OBJECTIVES

In this single-center study we reviewed our experience with a significant number of cardiac myxoma cases occurring over the past two decades.

PATIENTS AND METHODS

Cardiac myxomas represented 86% of all surgically treated cardiac tumors at our center. Specifically, there were 49 consecutive patients, each with at least one myxoma. A detailed clinical, immunological, and echocardiographic long-term examination of 37 patients revealed one recurrent myxoma.

RESULTS

Most myxomas originated from the left atrium (87.7%), but also much less frequently from the mitral valve (6.1%), from the right atrium (4.1%), and from the left and right atria (2.0%). The myxomas produced a prolapse into the left ventricle in 40.8% of the patients, mitral stenosis in 10.2%, and threatened left ventricular outflow tract obstruction in 2.0%. Multiple myxomas were found in 20.4% of the patients. Cardiac signs appeared in 93.9% of the patients. Preoperative embolic events had occurred in 26.5%. Immunologic alterations were present in 87.5%. For resection, a bilateral atriotomy was used. An additional aortotomy was needed to expose one mitral valve myxoma. Postoperatively, 81.1% of the patients remained without cardiac symptoms. The early mortality rate was 2.0% and the late mortality rate was 6.1%. Long-term prognosis was excellent with an actuarial survival rate of 0.74. Specific immunologic alterations were found in 71.4% of the patients. The actuarial freedom from reoperation of the myxoma was 0.96. The rate of reoperations was low with 2.0% after 24 years.

CONCLUSIONS

Myxomas were usually detected and operated on in symptomatic patients. A high index of suspicion seems important for early diagnosis. Immunologic findings may play an additional role in confirming the diagnosis and the recurrence of a myxoma. Immediate surgical treatment was indicated because of the high risk of embolization or of sudden cardiac death. Also, a familial genesis must be excluded in myxoma patients.

摘要

目的

在这项单中心研究中,我们回顾了过去二十年中大量心脏黏液瘤病例的经验。

患者与方法

心脏黏液瘤占我们中心所有手术治疗心脏肿瘤的86%。具体而言,有49例连续患者,每人至少有一个黏液瘤。对37例患者进行了详细的临床、免疫学和超声心动图长期检查,发现1例复发性黏液瘤。

结果

大多数黏液瘤起源于左心房(87.7%),但也较少起源于二尖瓣(6.1%)、右心房(4.1%)以及左、右心房(2.0%)。黏液瘤导致40.8%的患者出现左心室脱垂,10.2%的患者出现二尖瓣狭窄,2.0%的患者出现左心室流出道梗阻风险。20.4%的患者发现有多发性黏液瘤。93.9%的患者出现心脏体征。术前栓塞事件发生率为26.5%。免疫学改变发生率为87.5%。切除时采用双侧心房切开术。暴露一个二尖瓣黏液瘤需要额外进行主动脉切开术。术后,81.1%的患者无心脏症状。早期死亡率为2.0%,晚期死亡率为6.1%。长期预后良好,精算生存率为0.74。71.4%的患者发现有特定的免疫学改变。黏液瘤再次手术的精算无复发生存率为0.96。24年后再次手术率较低,为2.0%。

结论

黏液瘤通常在有症状的患者中被发现并进行手术。高度怀疑对于早期诊断似乎很重要。免疫学发现可能在确认黏液瘤的诊断和复发方面发挥额外作用。由于栓塞或心源性猝死风险高,应立即进行手术治疗

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