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The Journal of Thoracic and Cardiovascular Surgery, Vol 78, 573-575, Copyright © 1979 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
DA Ott, DA Cooley, P Angelini and RD Leachman
An unusual case of cor triatriatum dexter is presented. Abnormal
embryologic development of the eustachian valve caused nearly complete
septation of the right atrium in a 67-year-old woman. Multiple
supraventricular arrhythmias prompted clinical evaluation and diagnosis.
Surgical excision of the anomalous membrane resulted in complete relief
from arrhythmias and a clinical cure. Cor triatriatum dexter is rare and is
infrequently diagnosed before postmortem study; however, once the diagnosis
is extablished, the condition is amenable to a relatively simple surgical
correction. Supraventricular tachycardia has not previously been reported
to be associated with cor triatriatum dexter. We believe this is the first
case in which such arrhythmias led to early diagnosis and successful
surgical correction.
ARTICLES
Successful surgical correction of symptomatic cor triatriatum dexter
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A. Saylam, A. Aytac, G. Gursel, F. Ozmen, and M. E. Ozdogan Cor Triatriatum Sinistrum Case Report and Review of Current Concepts Vascular and Endovascular Surgery, January 1, 1983; 17(1): 50 - 58. [PDF] |
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