This Article  • References  • Full text PDF  • Send to a friend  • Save in My Folder  • Save to citation manager  • Permissions  Citing Articles  • Citing articles on HighWire  • Citing articles on Web of Science (10)  • Contact me when this article is cited  Related Content  • Similar articles in this journal  Social Bookmarking   What's this?

STANFORD S. KROOPF, M.D.; CARL A. PETERSON, M.D.

AMA Arch Intern Med. 1957;100(5):819-826.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Despite the fact that primary cardiac tumors have recently become so much less of a medical curiosity that individual cases are being reported less frequently, instances that present interesting and uncommon pathological and clinical features are still worthy of comment. This case of primary myxoma of the left atrium is interesting because of (1) the microscopic picture, which shows a high degree of cellular anaplasia, and (2) its clinical resemblance to coronary artery disease with myocardial infarction, progressive congestive failure, and pulmonary infarction, rather than the customary syndromes of mitral stenosis or embolic phenomena.

In 1942 Beck ¹ suggested surgical removal of myxomatous masses, and in 1950, Coulter ² drew attention to possible removal of such tumors through the atrium if recognized in time. With recent advances in cardiac surgery, such as the atrial well and the extracordial mechanical pumps,^3,4 Primary myxoma of the heart becomes a potentially curable . . . [Full Text PDF of this Article]

Author Affiliations
Palo Alto, Calif.

From the Departments of Medicine and Pathology, Palo Alto Hospital.

Footnotes
Submitted for publication April 4, 1957.

Supported by Medical Research Foundation for Palo Alto Hospital.

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter     What's this?