An Echocardiographic Study of a Rare Cause of Mitral Regurgitation: Hypoplastic Posterior Mitral Valve Leaflet.

IF 1.4 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Anatolian Journal of Cardiology Pub Date : 2024-12-20 DOI:10.14744/AnatolJCardiol.2024.4710
Ahmet Karaduman, Cemalettin Yılmaz, İsmail Balaban, Mehmet Aytürk, Münevver Sarı, Zübeyde Bayram, Alev Kılıçgedik, Gökhan Kahveci
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Abstract

Background: 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.

Methods: 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.

Results: 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).

Conclusion: 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.

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一种罕见的二尖瓣返流原因的超声心动图研究:二尖瓣后小叶发育不全。
背景:二尖瓣后小叶发育不全(PMVL)的确切病因尚未完全阐明;然而,它被假设起源于胎儿发育过程中发生的基因突变。在此,我们介绍了二尖瓣的解剖特征和相关的心脏病理患者的前冠状动脉瓣膜发育不全。方法:这项单中心回顾性研究纳入了2015年至2021年间在三级医疗机构就诊的患者。结果:有严重二尖瓣反流(MR)和非严重二尖瓣反流(MR)的患者共11例(25%),其中二尖瓣反流中位长度为5mm(5-6)。此外,10例患者伴有肌肉形成。我们发现13例患者有双尖瓣主动脉瓣(BAV),而第二常见的心脏先天性病理是7例患者的继发性房间隔缺损(ASD)。严重MR组二尖瓣前叶(AML)长度(P = .007)、AML脱垂(P < .001)、A2P2距离(P = .008)较高。严重MR组PMVL发育不全患者肌肉形成更为常见(P < .001)。结论:PMVL发育不全是一种罕见但重要的异常,可导致mr。虽然它可以与许多先天性疾病共存,但最常见的关联是BAV,其次是ASD。严重MR特别见于伴有二尖瓣环扩张、AML脱垂和肌肉形成的病例。
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来源期刊
Anatolian Journal of Cardiology
Anatolian Journal of Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.30
自引率
7.70%
发文量
270
审稿时长
12 weeks
期刊介绍: The Anatolian Journal of Cardiology is an international monthly periodical on cardiology published on independent, unbiased, double-blinded and peer-review principles. The journal’s publication language is English. The Anatolian Journal of Cardiology aims to publish qualified and original clinical, experimental and basic research on cardiology at the international level. The journal’s scope also covers editorial comments, reviews of innovations in medical education and practice, case reports, original images, scientific letters, educational articles, letters to the editor, articles on publication ethics, diagnostic puzzles, and issues in social cardiology. The target readership includes academic members, specialists, residents, and general practitioners working in the fields of adult cardiology, pediatric cardiology, cardiovascular surgery and internal medicine.
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