Idiopathic Dilatation of the Right Atrium: Diagnosis and Management

Author:

Rankovic-Nicic Ljiljana1,Dragicevic-Antonic Milica1,Loncar Goran12,Petrovic Masa12,Antonic Zelimir1,Bojic Milovan1

Affiliation:

1. 1Institute for Cardiovascular Diseases “Dedinje,” Belgrade, Serbia

2. 2 University of Belgrade Faculty of Medicine, Belgrade, Serbia

Abstract

Abstract Idiopathic dilatation of the right atrium is a rare condition with an unknown etiology. It is characterized by a significant enlargement of the right atrium without the presence of other valvopathies, intracardiac shunts, or pulmonary hypertension. This report presents the case of a 50-year-old woman with a significantly enlarged right atrium that was identified at birth; however, a definitive diagnosis was made later in life. The patient did not have any genetic diseases. Through the help of regular follow-up, anticoagulant therapy, previous radio-frequency ablation, and antiarrhythmic medications, she was able to carry a pregnancy to full term and live a regular life.

Publisher

Texas Heart Institute Journal

Subject

Cardiology and Cardiovascular Medicine

Reference14 articles.

1. Idiopathic enlargement of the right atrium;Sumner;Circulation,1965

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3. Prognosis and outcome of idiopathic dilatation of the right atrium in children. A cooperative study of 15 cases;Blaysat;Arch Mal Coeur Vaiss,1997

4. Idiopathic dilatation of the right atrium: clinical and diagnostic pitfalls—a series of 3 cases;Srinivasa;Echocardiography,2013

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