Pulcino Achille, Sordelli Chiara, Ismeno Gennaro, Tritto Francesco Paolo, Golino Paolo, Piazza Luigi
Department of Cardiac Surgery, S. Anna e S. Sebastiano Hospital, Caserta, Italy.
Monaldi Arch Chest Dis. 2011 Sep;76(3):146-8. doi: 10.4081/monaldi.2011.186.
We report a rare subtype of quadricuspid aortic valve (QAV) associated with moderate aortic regurgitation in a 17-year old woman symptomatic for palpitations. The patient was admitted to our department for cardiac evaluation due to a previous diagnosis of bicuspid aortic valve; she underwent a new two-dimensional echocardiography revealing a rare type of quadricuspid aortic valve with a moderate regurgitation. For further investigating potentially associated abnormalities, patient was referred to Cardiac MRI; MRI showed no other abnormalities and confirmed echocardiographic findings. Quadricuspid aortic valve is a rare form of congenital valvular anomaly often occasionally diagnosed. In most cases this malformation causes a valve dysfunction, commonly aortic regurgitation, and can be associated with other cardiac abnormalities such as ventricular or atrial septal defect, anomalies of coronary arteries, patent ductus arteriosus, subaortic fibromuscolar stenosis and mitral valve malformation.
我们报告了一名17岁有心悸症状的女性,其患有与中度主动脉瓣反流相关的罕见亚型四叶式主动脉瓣(QAV)。该患者因先前诊断为二叶式主动脉瓣而入住我科进行心脏评估;她接受了新的二维超声心动图检查,结果显示为一种罕见类型的四叶式主动脉瓣伴中度反流。为进一步调查潜在的相关异常情况,患者接受了心脏磁共振成像(MRI)检查;MRI未显示其他异常,并证实了超声心动图检查结果。四叶式主动脉瓣是一种罕见的先天性瓣膜异常形式,常偶尔被诊断出来。在大多数情况下,这种畸形会导致瓣膜功能障碍,通常是主动脉瓣反流,并且可能与其他心脏异常有关,如室间隔或房间隔缺损、冠状动脉异常、动脉导管未闭、主动脉下纤维肌性狭窄和二尖瓣畸形。