Tessitore Elena, Müller Hajo, Nganou-Gnindjio Chris Nadege, Grisel Philippe, Šekoranja Lučka
Division of Cardiology, University Hospital of Geneva, Geneva, Switzerland.
Echocardiography. 2015 Mar;32(3):595-7. doi: 10.1111/echo.12793. Epub 2014 Oct 7.
Quadricuspid aortic valve (QAV) is a rare congenital heart defect, often related to severe aortic regurgitation, and usually detected by echocardiography or at the time of aortic valve surgery. We report a case of an interesting and extremely rare variant of "false" QAV, detected preoperatively by transthoracic and transesophageal echocardiography, in a severely symptomatic patient, admitted to our hospital for dyspnea. Three leaflets of aortic valve appeared quadricuspid, because the left coronary cusp was divided into 2 parts, as confirmed by MRI and pathology. Most frequently, QAV presents with all 4 leaflets equal in size.
四叶式主动脉瓣(QAV)是一种罕见的先天性心脏缺陷,常与严重的主动脉瓣反流相关,通常通过超声心动图或在主动脉瓣手术时发现。我们报告一例有趣且极其罕见的“假性”QAV变异病例,该病例通过经胸和经食管超声心动图在术前被发现,患者因呼吸困难入院,症状严重。主动脉瓣的三个瓣叶看似四叶式,因为左冠状动脉瓣叶被分为两部分,这一点经磁共振成像(MRI)和病理学证实。最常见的情况是,QAV的四个瓣叶大小相等。