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J Thorac Cardiovasc Surg 2007;134:250-251
© 2007 The American Association for Thoracic Surgery
Brief Communication |
Department of Cardiovascular Surgery, Hospital Clinic Barcelona, University of Barcelona, Barcelona, Spain.
Received for publication November 3, 2006; accepted for publication November 16, 2006. * Address for reprints: Stefano Congiu, MD, Universite degli studi di Parma, Department of Cardiac Surgery, Via Gramsci 14, Parma 43100, Italy. (Email: scongiu@tiscali.it).
| The first 20% of the full text of this article appears below. |
Double-orifice mitral valve (DOMV) is a rare congenital abnormality. Isolated occurrences of this defect are uncommon, and they are usually associated with other congenital heart defects.
Clinical Summary
A 64-year-old woman was found to have a heart murmur suggestive of mitral regurgitation during a routine clinical examination. The patient had a past history of arterial hypertension. She complained of gradually progressive dyspnea for 6 months before admission.
Transesophageal echocardiography showed dilatation of the left and right atria and ventricles, severe mitral regurgitation, moderate tricuspid regurgitation, a large aneurysm of the interatrial septum, and severe pulmonary hypertension. The mitral valve was divided in two by the presence of a middle structure, which created a functional double-orifice valve (Figure 1).
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J. Thorac. Cardiovasc. Surg. 2007 134: 250-251.
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