[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.205.8.87. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
March 1959

Cardiac MyxomaSurgical Treatment in Four Cases

Author Affiliations

Houston, Texas
From the Cora and Webb Mading Department of Surgery, Baylor University College of Medicine, and the Surgical Service of the Jefferson Davis, Methodist, and Veterans Administration Hospitals.

AMA Arch Surg. 1959;78(3):410-417. doi:10.1001/archsurg.1959.04320030054010
Abstract

Primary tumors of the heart, although rare, are being recognized more frequently as a result of increasing interest in cardiovascular surgery and improvement in diagnostic techniques. Intracardiac myxomata comprise some 50% of primary cardiac tumors and are located in the left atrium in approximately 75% of cases. Myxomata occur in persons of all ages, including the newborn, but the majority of patients are between 30 and 60 years of age. The lesion occurs in females three times as frequently as in males. Although the majority of these lesions arise at the fossa ovalis, in some cases the point of attachment is the valve of the inferior vena cava and the left ventricle.

Tumors of the heart drew the attention of pathologists as early as the 17th century, as evidenced by the writings of Malpighi, in 1666, in "De polypo cordis dissertatio," and many others, quoted at length in the monograph

First Page Preview View Large
First page PDF preview
First page PDF preview
×