Tukeni Kedir Negesso, Bezabih Kidus Tesfaye, Woyimo Tamirat Godebo, Asefa Elsah Tegene
Jimma University, Jimma, Ethiopia.
Ludwig Maximilian University of Munich, Munich, Germany.
J Med Case Rep. 2025 Jun 4;19(1):265. doi: 10.1186/s13256-025-05292-1.
Mitral blood cyst with atrial septal aneurysm is a unique instance of rare occurrence in medical literature. It is crucial for the discipline of cardiology to address the special difficulties that come with diagnosing and treating these two diseases together. The goal of this case report is to provide a comprehensive overview of the clinical presentation, diagnostic challenges, and treatment strategies for this uncommon cardiac disease in a resource-limited setting.
This is a case involving a 50-year-old Ethiopian female patient referred to our hospital for cardiac evaluation. She presented with intermittent palpitation to a nearby health center, which was diagnosed as rheumatic heart disease, for which she was on intramuscular benzathine penicillin injection on a monthly basis. Otherwise, she had no history suggestive of acute rheumatic fever and no chest pain, body swelling, orthopnea, or paroxysmal nocturnal dyspnea, historically or on current presentation. Evaluations revealed that her chest was clear and resonant with good air entry, and flat jugular venous pressure, but she had a grade III pansystolic murmur best heard at the apex that radiates to the left axilla. No other pertinent physical examination findings were discovered. Echocardiographic evaluation revealed a tiny cyst at the apex of posterior mitral valve leaflet with interatrial septal bulging into the right atrium.
Cardiac blood cysts are an uncommon congenital cardiac condition that can lead to stroke and other potentially fatal consequences, especially if they are situated on the mitral valve. With improved specialists and low-risk procedures, surgical removal is advised. Given the patient's state, a proper diagnosis was therefore essential to provide her with accessible management options in this setting while she waits for a definitive surgical treatment in case the need arises.
二尖瓣血囊肿合并房间隔瘤是医学文献中罕见的独特病例。对于心脏病学科而言,应对同时诊断和治疗这两种疾病所带来的特殊困难至关重要。本病例报告的目的是在资源有限的情况下,全面概述这种罕见心脏病的临床表现、诊断挑战及治疗策略。
这是一例涉及一名50岁埃塞俄比亚女性患者的病例,她因心脏评估被转诊至我院。她因间歇性心悸前往附近的健康中心就诊,被诊断为风湿性心脏病,为此她每月接受苄星青霉素肌肉注射治疗。此外,无论从病史还是当前表现来看,她均无提示急性风湿热的病史,也无胸痛、身体肿胀、端坐呼吸或阵发性夜间呼吸困难。评估发现她的胸部清晰且叩诊呈清音,呼吸音良好,颈静脉压正常,但在心尖部可闻及III级全收缩期杂音,向左腋窝传导,未发现其他相关体格检查异常。超声心动图评估显示二尖瓣后叶尖部有一个微小囊肿,房间隔向右侧心房膨出。
心脏血囊肿是一种罕见的先天性心脏病,可导致中风及其他潜在致命后果,尤其是位于二尖瓣时。鉴于有经验丰富的专家和低风险手术,建议进行手术切除。考虑到患者的情况,因此在这种情况下进行正确诊断对于为她提供可及的管理选择至关重要,以便她在必要时等待确定性手术治疗期间能得到妥善处理。