Karaduman Ahmet, Yılmaz Cemalettin, Balaban İsmail, Aytürk Mehmet, Sarı Münevver, Bayram Zübeyde, Kılıçgedik Alev, Kahveci Gökhan
Department of Cardiology, University of Health Sciences, Hamidiye Faculty of Medicine, Koşuyolu Heart Training and Research Hospital, İstanbul, Türkiye.
Department of Cardiology, Muş State Hospital, Muş, Türkiye.
Anatol J Cardiol. 2024 Dec 20;29(3):124-31. doi: 10.14744/AnatolJCardiol.2024.4710.
The precise etiology of hypoplasia of the posterior mitral valve leaflet (PMVL) remains incompletely elucidated; however, it has been hypothesized to stem from genetic mutations occurring during fetal development. Herein, we present the anatomical characteristics of the mitral valve and associated cardiac pathologies in patients with hypoplastic PMVL.
This single-center retrospective study involved patients who presented between 2015 and 2021 at a tertiary healthcare facility. Among the cohort, 44 individuals had hypoplastic PMVL and were divided into 2 groups: those with severe mitral regurgitation (MR) and those with non-severe MR.
Among the patients, 11 (25%) had severe MR. The median lengths for the PMVL was 5 mm (5-6). Moreover, 10 patients had concomitant muscular formation. We found that 13 patients had bicuspid aortic valve (BAV), while the second most common concomitant cardiac congenital pathology was secundum atrial septal defect (ASD) in 7 patients. The anterior mitral leaflet (AML) length (P = .007), AML prolapse (P < .001), and A2P2 distance (P = .008) were higher in the group with severe MR. In addition, muscular formation was more common in patients with hypoplastic PMVL with severe MR (P < .001).
Hypoplastic PMVL is a rare but significant anomaly that causes MR. While it can coexist with numerous congenital conditions, the most frequent associations include BAV and, secondly, ASD. Severe MR is particularly observed in cases accompanied by dilated mitral annulus, AML prolapse, and muscular formation.
二尖瓣后叶发育不全的确切病因仍未完全阐明;然而,据推测其源于胎儿发育期间发生的基因突变。在此,我们呈现二尖瓣发育不全患者的二尖瓣解剖特征及相关心脏病变。
这项单中心回顾性研究纳入了2015年至2021年在一家三级医疗机构就诊的患者。在该队列中,44例患者存在二尖瓣后叶发育不全,并被分为两组:重度二尖瓣反流(MR)组和非重度MR组。
在这些患者中,11例(25%)有重度MR。二尖瓣后叶的中位长度为5毫米(5 - 6)。此外,10例患者伴有肌肉形成。我们发现13例患者有二叶式主动脉瓣(BAV),而第二常见的合并心脏先天性病变是7例患者中的继发孔房间隔缺损(ASD)。重度MR组的二尖瓣前叶(AML)长度(P = .007)、AML脱垂(P < .001)和A2P2距离(P = .008)更高。此外,重度MR的二尖瓣后叶发育不全患者中肌肉形成更为常见(P < .001)。
二尖瓣后叶发育不全是一种罕见但重要的导致MR的异常情况。虽然它可与多种先天性疾病共存,但最常见的关联包括BAV,其次是ASD。重度MR尤其见于伴有二尖瓣环扩张、AML脱垂和肌肉形成的病例。