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María Elena Arnáiz-García Javier Arnáiz#

Ana María Arnáiz-García*

Jose Aurelio Sarralde Agüayo† Department of Cardiac Surgery, University Hospital of Salamanca, Spain;

#Department of Radiology, University Hospital Marqués de Valdecilla, Spain; *Department of Internal Medicine, University Hospital Marqués de Valdecilla, Spain;

Department of Cardiovascular Surgery, University Hospital Marqués de Valdecilla, Spain

Türk Kardiyol Dern Arş - Arch Turk Soc Cardiol 2013;41(8):780 doi: 10.5543/tkda.2013.60598

A 52-year-old woman, with a previous history of hypertension, was admitted to our institution presenting exer-tional dyspnea. A comprehensive study was per-formed includ-ing a cardiology examination and echocardiography. Transesophageal echocardiography detected a quad-ricuspid aortic valve with a central severe aortic valve insufficiency. Moreover, a discrete dilation of the aortic root was seen. Left ventricular ejection fraction was in normal range. A computed tomography scan was performed especially to recognize any displacement of the coro-nary ostia and evaluate the aortic valve (Fig. A). No abnormality of coronary artery origin was confirmed.

Surgical treatment was proposed, and the patient underwent open-heart surgery. Quadricuspid valve was confirmed (Fig. B). An aortoplasty to reduce the

ascend-ing aorta and a mechanical aortic valve replacement were performed. The postoperative course was favor-able, and the patient had an uneventful recovery. Post-operative echocardiography assessment confirmed normal prosthetic aortic valve function and left ven-tricular ejection fraction. Quadricuspid aortic valve is a rare congenital abnormality, with an estimated inci-dence of 0.04%. In approximately 80-90% of cases, it is related to an aortic valve dysfunction. Quadricuspid aortic valve is usually associated with additional mal-formations, mainly related to the origin of coronary arteries. Due to the presence of an additional leaflet, absence or displacement of coronary ostia has been found in 10% of cases. It is of utmost importance to prevent coronary ostia obstruction with valve pros-thesis implantation, and to plan myocardial protection during cardiopulmonary bypass. In the presence of prior surgery for congenital aortic valve abnormalities and regardless of patient age, we highlight the neces-sity to perform a careful evaluation of the coronary anatomy.

780

Massive aortic regurgitation in the background of a quadricuspid aortic valve

Dört yaprakçıklı aort kapağında masif aort yetersizliği

Figures– (A) Computed tomography short-axis image of the four aortic valve cusps. (B) Intraoperative view of the quadricuspid aortic valve. RV: Right ventricle; AA: Ascending aorta; QAV: Quadricuspid aortic valve (*aortic leaflet).

A B

RV

AA

* OAV

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