Eto Hiroaki, Uzu Kenzo, Nagasawa Yoshinori, Shimokawa Yasushi, Okubo Hideaki, Shimizu Hiroki
Department of Cardiology, Konan Medical Center, Kobe, Japan.
J Cardiol Cases. 2023 Oct 23;29(1):39-42. doi: 10.1016/j.jccase.2023.10.001. eCollection 2024 Jan.
Accessory mitral valve tissue (AMVT) is a rare congenital anomaly that sometimes causes left ventricular outflow tract (LVOT) obstruction. We report the case of a 72-year-old woman with hypertrophic obstructive cardiomyopathy (HOCM) complicated by AMVT. The patient presented at our hospital with palpitations and shortness of breath. Transthoracic echocardiography revealed a diagnosis of HOCM and an abnormal structure inside the LVOT. Transesophageal echocardiography revealed an AMVT. We initially treated the patient with oral medication, but due to side effects, the patient could not take the target dose and her symptoms did not improve. We suggested surgical treatment, but the patient refused. By evaluating the relationship between AMVT and the surrounding tissues using three-dimensional transesophageal echocardiography, we determined that percutaneous septal myocardial ablation (PTSMA) might be successful. The first PTSMA was not effective, but the second procedure showed significant improvement in the pressure gradient and symptoms. The patient with HOCM and concomitant AMVT had a severe LVOT pressure gradient, and PTSMA was performed with excellent results. Since we experienced a rare case and were able to treat it percutaneously, we report our findings in relation to the literature.
This case study highlights successful use of percutaneous septal myocardial ablation (PTSMA) in treating a patient with hypertrophic obstructive cardiomyopathy (HOCM) and accessory mitral valve tissue (AMVT). The key objective is to understand PTSMA can be an effective treatment option for HOCM with Type IIa AMVT, characterized by the attachment only to the mitral leaflets, when surgical intervention is not preferred, enhancing management of this rare condition.
二尖瓣附属组织(AMVT)是一种罕见的先天性异常,有时会导致左心室流出道(LVOT)梗阻。我们报告一例72岁女性肥厚型梗阻性心肌病(HOCM)合并AMVT的病例。该患者因心悸和气促前来我院就诊。经胸超声心动图显示诊断为HOCM,且LVOT内结构异常。经食管超声心动图显示存在AMVT。我们最初对患者进行口服药物治疗,但由于副作用,患者无法服用目标剂量药物,症状也未改善。我们建议手术治疗,但患者拒绝。通过三维经食管超声心动图评估AMVT与周围组织的关系,我们确定经皮室间隔心肌消融术(PTSMA)可能成功。首次PTSMA无效,但第二次手术使压力阶差和症状有显著改善。该HOCM合并AMVT患者存在严重的LVOT压力阶差,行PTSMA取得了良好效果。由于我们遇到了一个罕见病例并能够通过经皮方式进行治疗,我们结合文献报告我们的发现。
本病例研究强调了经皮室间隔心肌消融术(PTSMA)成功用于治疗肥厚型梗阻性心肌病(HOCM)合并二尖瓣附属组织(AMVT)患者。关键目标是了解当手术干预不可取时,PTSMA对于IIa型AMVT(其特征仅附着于二尖瓣叶)的HOCM可以是一种有效的治疗选择,从而加强对这种罕见疾病的管理。