Cardiac Myxoma
- 1 December 1970
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 23 (6) , 558-567
- https://doi.org/10.1001/archneur.1970.00480300080011
Abstract
THERE are now over 350 reported cases of cardiac myxoma, a slowly-growing intracavitary tumor, most frequently occurring in the left atrium.1,2Cardiac myxomas manifest themselves clinically by obstruction of cardiac flow, by constitutional effects, and by embolization. Systemic emboli have been reported in up to 45% of patients with left atrial myxoma.3-5In cases where inconspicuous cardiac symptoms and signs are combined with multiple cerebral emboli, a difficult diagnostic problem confronts the clinician. Maroon and Campbell6have pointed out the importance of atrial myxoma as one of the potentially treatable causes of cerebrovascular occlusion. The present report describes the case of a young woman in whom a left atrial myxoma with disseminated emboli gave rise to pathologic changes in cerebral vessels unlike any that we had previously seen or that had been described by others. Because of the puzzling clinical course, the striking abnormalities visualized byKeywords
This publication has 9 references indexed in Scilit:
- Cholesterol emboli in cerebral arteries as a complication of retrograde aortic perfusion during cardiac surgeryNeurology, 1970
- Cerebral Angiography in Cardiac MyxomaRadiology, 1970
- Atrial myxoma: a treatable cause of stroke.Journal of Neurology, Neurosurgery & Psychiatry, 1969
- Cardiac Myxoma. A morphologic and histogenetic appraisalCancer, 1968
- Profile of atrial myxomaThe American Journal of Cardiology, 1968
- Clinical aspects of cardiac tumorsThe American Journal of Cardiology, 1968
- Pathology of cardiac tumorsThe American Journal of Cardiology, 1968
- Radiologic Observations in Cerebral Embolization from Left Heart MyxomasRadiology, 1966
- Cardiac Myxomas with Systemic EmbolizationCirculation, 1962