Venkatesh Prashanth, Tan Weiyi, Bravo-Jaimes Katia, Aboulhosn Jamil
Division of Cardiology, Department of Medicine, Ahmanson-UCLA Adult Congenital Heart Disease Center, David Geffen School of Medicine, University of California, Los Angeles, 200 Medical Plaza, Suite 202, Los Angeles, CA 90095, USA.
Eur Heart J Case Rep. 2022 Jun 15;6(7):ytac237. doi: 10.1093/ehjcr/ytac237. eCollection 2022 Jul.
Anomalous coronary origin from the left ventricular outflow tract (LVOT) is an exceedingly rare condition thought to be associated with the bicuspid aortic valve (BAV). While the malignant presentation of this entity has been described, its pathophysiology and diagnostic evaluation are poorly understood.
A 33-year-old woman status post Ross procedure in childhood for congenital aortic stenosis due to BAV with presumed common origin of right and left coronary arteries based on single coronary ostium seen on aortic valve inspection, presented with symptomatic pulmonary regurgitation and stenosis. Invasive left coronary angiography revealed retrograde filling of the right coronary artery (RCA) with systolic washout of contrast indicating a patent RCA ostium. No RCA ostium was found on aortic root injection, but an injection into the LVOT revealed an RCA ostium below the aortic valve. Selective RCA angiography revealed pulsatile antegrade flow down the RCA occurring during systole. There was no anatomic RCA stenosis. We proceeded with valve-in-valve TcPVR. The patient had significant improvement of symptoms and RCA reimplantation was hence deferred.
This case is the first of an anomalous coronary artery arising from the LVOT diagnosed in a patient after the Ross procedure. Our angiograms shed light on the unusual physiology of coronary filling during systole and ischaemia arising from inadequate perfusion gradient between the left ventricle and the coronary during systole, leading to collateralization despite the lack of anatomic stenosis. We urge consideration of this potentially malignant entity in any symptomatic patient, especially with concomitant BAV.
左心室流出道(LVOT)冠状动脉起源异常是一种极为罕见的疾病,被认为与二叶式主动脉瓣(BAV)有关。虽然已经描述了该实体的恶性表现,但其病理生理学和诊断评估仍知之甚少。
一名33岁女性,儿童时期因BAV导致先天性主动脉狭窄接受Ross手术,根据主动脉瓣检查所见的单一冠状动脉开口,推测左右冠状动脉共同起源。现出现有症状的肺动脉反流和狭窄。有创左冠状动脉造影显示右冠状动脉(RCA)逆行充盈,造影剂在收缩期冲刷,提示RCA开口通畅。主动脉根部注射未发现RCA开口,但向LVOT注射显示主动脉瓣下方有RCA开口。选择性RCA造影显示收缩期RCA有搏动性顺行血流。无解剖学上的RCA狭窄。我们进行了经导管肺动脉瓣置换术(TcPVR)。患者症状有显著改善,因此推迟了RCA再植入。
该病例是Ross手术后诊断出的首例LVOT冠状动脉起源异常病例。我们的血管造影揭示了收缩期冠状动脉充盈的异常生理情况,以及收缩期左心室与冠状动脉之间灌注梯度不足导致的缺血,尽管没有解剖学狭窄,但仍导致侧支循环形成。我们敦促对任何有症状的患者,尤其是合并BAV的患者,考虑这种潜在的恶性实体。