| Literature DB >> 27278941 |
Takeshi Masaki1, Masami Nishino2, Masayuki Taniike1, Nobuhiko Makino1, Hiroyasu Kato1, Yasuyuki Egami1, Ryu Shutta1, Hitoshi Yamaguchi1, Jun Tanouchi1, Yoshio Yamada1.
Abstract
Quadricuspid aortic valve (QAV) is a rare congenital aortic valve anomaly. We present two cases of QAV diagnosed by using echocardiography including transesophageal echocardiography (TEE) and cardiac computed tomography (CT). The first case, QAV with four equal-sized cusps, was identified in a 58-year-old man. The second case, QAV with a small accessory cusp between the right coronary and non-coronary cusp, was identified in a 42-year-old man. TEE and cardiac CT could lead to accurate diagnosis of QAV. QAV in these two patients could be diagnosed before indication for surgery but it is necessary to continue careful follow-up.Entities:
Keywords: Aortic regurgitation; Congenital cardiac anomaly; Quadricuspid aortic valve; Transesophageal echocardiography; Transthoracic echocardiography
Year: 2010 PMID: 27278941 DOI: 10.1007/s12574-010-0039-8
Source DB: PubMed Journal: J Echocardiogr ISSN: 1349-0222