Prasad Krishna, Gupta Himanshu, Sihag Bhupendra Kumar, Bootla Dinakar, Panda Prashant, Sharma Arun, Chauhan Rajeev, Gawalkar Atit, Dahiya Neelam
Department of Cardiology, Post Graduate Institute of Medical Education and Research, Sector 12, 160012, Chandigarh, India.
Department of Radiodiagnosis and Imaging, Post Graduate Institute of Medical Education and Research, Sector 12, 160012, Chandigarh, India.
Eur Heart J Case Rep. 2021 Feb 20;5(2):ytab066. doi: 10.1093/ehjcr/ytab066. eCollection 2021 Feb.
Submitral aneurysm is a rare disease initially described in the African population. It is usually considered congenital in origin, due to a defect in the posterior portion of the mitral annulus. However, it can be seen in other diseases like ischaemic heart disease, rheumatic heart disease, infective endocarditis, tuberculosis, and syphilis.
Case 1 was a 29-year-old female, hypertensive undergoing maintenance haemodialysis for chronic kidney disease and on anti-tubercular therapy. She was found to have a large submitral aneurysm with severe mitral regurgitation, moderate left ventricular dysfunction, and pericardial effusion on echocardiogram. Case 2 was a 58-year-old gentleman presented with inferior wall ST-elevation myocardial infarction and was thrombolyzed with streptokinase for the same. Echocardiogram done 6 months later for evaluation of dyspnoea showed a large inferobasal aneurysm. Case 3 was a 56-year-old hypertensive presented with dyspnoea on exertion and echocardiogram showed a large posterolateral region with transmural late gadolinium enhancement. Case 4 was a 13-year-old boy presented with fever and cerebrovascular accident. Echocardiogram revealed vegetation in the mitral valve and a small submitral aneurysm with vegetation inside it.
Submitral aneurysm is usually considered congenital in origin. However, it can be due to ischaemic heart disease, rheumatic heart disease, Takayasu arteritis, and tuberculosis. Top dimensional echocardiogram is the investigation of choice. Cardiac magentic resonance imaging helps in identifying the underlying aetiology and delineating the surrounding structures.
二尖瓣下动脉瘤是一种罕见疾病,最初在非洲人群中被描述。它通常被认为起源于先天性,是由于二尖瓣环后部的缺陷所致。然而,它也可见于其他疾病,如缺血性心脏病、风湿性心脏病、感染性心内膜炎、结核病和梅毒。
病例1是一名29岁女性,因慢性肾病接受维持性血液透析且正在接受抗结核治疗,患有高血压。超声心动图检查发现她有一个巨大的二尖瓣下动脉瘤,伴有严重二尖瓣反流、中度左心室功能障碍和心包积液。病例2是一名58岁男性,因下壁ST段抬高型心肌梗死就诊,并接受了链激酶溶栓治疗。6个月后为评估呼吸困难而进行的超声心动图检查显示有一个巨大的下基底动脉瘤。病例3是一名56岁高血压患者,表现为劳力性呼吸困难,超声心动图显示后外侧区域较大,有透壁性延迟钆增强。病例4是一名13岁男孩,出现发热和脑血管意外。超声心动图显示二尖瓣有赘生物,二尖瓣下有一个小动脉瘤,内部也有赘生物。
二尖瓣下动脉瘤通常被认为起源于先天性。然而,它也可能由缺血性心脏病、风湿性心脏病、高安动脉炎和结核病引起。经胸超声心动图是首选的检查方法。心脏磁共振成像有助于确定潜在病因并描绘周围结构。