A Rare Case of Congestive Heart Failure due to Isolated Aortic Valve Disease in a Middle-Aged Man Secondary to Rheumatic Fever.

Varshitha Tumkur Panduranga, Asher Gorantla, Asad Ahmed, Jacob Sabu, Mary Mallappallil, Sabu John
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Abstract

Rheumatic heart disease (RHD) is commonly seen in people from developing and low-income countries. More cases are being recorded in developed countries due to migration and globalization. RHD develops in people with a history of rheumatic fever; it is an autoimmune response to group A streptococcal infection due to similarities at the molecular level. Congestive heart failure, arrhythmia, atrial fibrillation, stroke, and infective endocarditis are a few of the many complications associated with RHD. Here we present a case of a 48-year-old male with a past medical history of rheumatic fever at the age of 12 years, who presented to the emergency room (ER) complaining of bilateral ankle swelling, dyspnea on exertion, and palpitations. The patient was tachycardic with a heart rate of 146 beats per minute and tachypneic with a respiratory rate of 22 breaths per minute. On physical exam, there was a harsh systolic and diastolic murmur at the right upper sternal border. A 12-lead electrocardiogram (EKG) revealed atrial flutter with a variable block. Chest X-ray revealed an enlarged cardiac silhouette with a pro-brain natriuretic peptide (proBNP) of 2,772 pg/mL (normal ≤ 125 pg/mL). The patient was stabilized with metoprolol and furosemide and was admitted to the hospital for further investigation. Transthoracic echocardiogram showed left ventricular ejection fraction (LVEF) of 50-55% with severe concentric hypertrophy of the left ventricle with a severely dilated left atrium. Increased thickness of the aortic valve with severe stenosis and a peak gradient of 139 mm Hg and a mean gradient of 82 mm Hg was noted. The valve area was measured to be 0.8 cm2. Transesophageal echocardiogram showed a tri-leaflet aortic valve with commissural fusion of valve cusps with severe leaflet thickening consistent with rheumatic valve disease. The patient underwent tissue aortic valve replacement with a bioprosthetic valve. The pathology report showed extensive fibrosis and calcification of the aortic valve. The patient came in for a follow-up visit 6 months later and expressed feeling better and more active.

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一例罕见的充血性心力衰竭由于孤立主动脉瓣疾病继发于风湿热的中年男子。
风湿性心脏病常见于发展中国家和低收入国家的人群。由于移民和全球化,发达国家记录的病例越来越多。有风湿热病史的人会出现RHD;由于分子水平上的相似性,它是对A组链球菌感染的自身免疫反应。充血性心力衰竭、心律失常、心房颤动、中风和感染性心内膜炎是与RHD相关的许多并发症中的一些。在这里,我们提出一个48岁的男性病例,他在12岁时有风湿热病史,他到急诊室(ER)抱怨双侧踝关节肿胀,用力时呼吸困难和心悸。患者心跳过速,每分钟心跳146次,呼吸过速,每分钟呼吸22次。体格检查发现,在右胸骨上缘有严重的收缩期和舒张期杂音。12导联心电图(EKG)显示心房扑动伴可变阻滞。胸部x线显示心脏轮廓增大,proBNP为2,772 pg/mL(正常≤125 pg/mL)。患者在美托洛尔和速尿治疗下病情稳定,并入院接受进一步检查。经胸超声心动图显示左心室射血分数(LVEF)为50-55%,左心室严重同心肥厚,左心房严重扩张。主动脉瓣厚度增加,严重狭窄,峰值梯度为139毫米汞柱,平均梯度为82毫米汞柱。测量出瓣膜面积为0.8 cm2。经食管超声心动图显示三瓣主动脉瓣,瓣尖融合,伴有严重的瓣叶增厚,符合风湿性瓣膜病。患者接受了生物瓣膜置换术。病理报告显示主动脉瓣广泛纤维化和钙化。患者在6个月后进行了随访,并表示感觉更好,更活跃。
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