一例罕见的卢滕巴赫氏综合征并发低梯度严重二尖瓣狭窄:病例报告和文献综述

Samah El-Mhadi, Belghait El Hajjaj, Nabil Laktib, Latifa Oukerraj, M. Cherti
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引用次数: 0

摘要

卢滕巴赫综合征是指房间隔缺损和二尖瓣狭窄的罕见合并症。尽管这种病症具有独特的临床、辅助临床和治疗意义,但其诊断率仍然很低。 我们报告了一例 60 岁女性急性充血性心力衰竭的病例。检查发现她合并有低梯度重度风湿性二尖瓣狭窄和房间隔缺损。尽管医疗团队对她的病情进行了保守治疗,并建议她接受手术治疗,但患者还是不听医嘱选择了自行出院。6 个月后,她去世了。 在我们的临床实践中,卢滕巴赫综合征仍然是一种罕见病。一旦确诊为低梯度重度二尖瓣狭窄,就必须寻找伴发的房间隔缺损,尤其是在右心室明显增大或功能障碍的早期,或者二尖瓣面积和二尖瓣传导瓣梯度之间存在耐人寻味的不一致时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Lutembacher’s Syndrome Presenting with Low-Gradient Severe Mitral Stenosis: Case Report and Literature Overview
Lutembacher's syndrome refers to the rare combination of atrial septal defect and mitral stenosis. This condition is still underdiagnosed despite its distinct clinical, paraclinical and therapeutic implications. We report the case of a 60-year-old woman presenting with acute congestive heart failure. Investigations revealed the combination of low-gradient severe rheumatic mitral stenosis and ostium secundum atrial septal defect. Despite the medical team's conservative management of her condition and recommendation for surgical intervention, the patient chose to discharge herself against medical advice. She deceased 6 months later. Lutembacher's syndrome continues to be a rare condition in our practice. Once low-gradient severe mitral stenosis is diagnosed, it's essential to search for an associated atrial septal defect, especially when there is an early onset of significant right ventricular enlargement or dysfunction, or when an intriguing inconsistency exists between the mitral area and the transmitral gradient.
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