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DOI 10.1016/s1010-7940(02)00592-4

Медицинская библиотека · European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery · 2002

Cardiac myxomas: 24 years of experience in 49 patients.

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

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Аннотация

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.

Для цитирования: Keeling I M, Oberwalder P, Anelli-Monti M, Schuchlenz H, Demel U, Tilz G P, Rehak P, Rigler B. Cardiac myxomas: 24 years of experience in 49 patients.. European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 2002. DOI: 10.1016/s1010-7940(02)00592-4.

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