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J Thorac Cardiovasc Surg 2004;128:753-756
© 2004 The American Association for Thoracic Surgery
Brief communication |
a Division of Cardiac Surgery, University of Verona, Verona, Italy
Received for publication February 10, 2004; revisions received March 5, 2004; accepted for publication March 15, 2004.
* Address for reprints: Giovanni Battista Luciani, MD, Division of Cardiac Surgery, University of Verona, O. C. M. Piazzale Stefani 1, Verona, 37126 Italy
gbluciani@yahoo.com
| The first 300 words of the full text of this article appear below. |
Aortic valve replacement with the pulmonary autograft (ie, the Ross operation) is generally associated with satisfactory early and late results. Complications, however, can occur, including the tendency of the pulmonary autograft root to dilate with time.1 Whereas neoaortic root dilatation might be observed in as many as one third of patients late after the Ross operation,2 uncertainty still exists as to the rate of progression toward true aneurysmal disease (aortic diameter
5 cm).1,2 Furthermore, the actual risk of complications, such as neoaortic rupture or dissection, is also unknown. The yet undefined natural history of root dilatation after the Ross operation, the often satisfactory competence of the pulmonary autograft valve, the scarcity of valid therapeutic alternatives (particularly in the infant and child), and the complexityrisk of reintervention have thus far delayed standardization of therapeutic indications. In particular, timing and technique of reoperation on the aneurysmal neoaortic root are still controversial.1,2
Here we present a case of potentially lethal evolution of progressive pulmonary autograft dilatation (ie, neoaortic root dissection) successfully treated with valve-sparing root replacement. The implications in terms of natural history and indications for reintervention are discussed.
Clinical summary
A 29-year-old man with a long-standing history of aortic valve regurgitation on the bicuspid aortic valve and mild dilatation of the aortic root underwent elective aortic root replacement with the pulmonary autograft on October 18, 1994. The right ventricular outflow tract was reconstructed with a 28-mm pulmonary homograft. Postoperative recovery was uneventful, and discharge echocardiography showed competent semilunar valves and normal aortic root diameter. Two years after the operation, moderate dilatation of the aortic root (maximum diameter, 46 mm) was identified at yearly echocardiographic examination. The aortic valve, however, was competent, and the patient was completely symptom free. Subsequent examinations confirmed progressive root dilatation, which reached true aneurysmal dimensions 8 years after the operation.
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