A Case of Isolated Bicuspid Pulmonic Valve and Pulmonary Artery Aneurysm

M. Sahebjam, Neda Toofaninejad
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Abstract

A 33-year-old woman with a history of thyroid surgery for thyroid cancer and radioactive iodine therapy was referred for echocardiography due to dyspnea on exertion. Transthoracic echocardiography showed normal left ventricular size and function (the ejection fraction = 55%), a prolapsing mitral valve with redundant chordae, mild mitral regurgitation, a tricuspid aortic valve, mild aortic insufficiency, and mild tricuspid regurgitation. The most remarkable echocardiographic findings were moderate right ventricular dilation with mild systolic dysfunction, moderate right atrial dilation, an aneurysmal pulmonary artery (the main pulmonary artery = 47 mm), mild pulmonary stenosis (the peak gradient = 22 mmHg), and severe pulmonary regurgitation (the vena contracta = 6–7 mm and the pressure half time = 105 ms). Transesophageal echocardiography with the use of 3D modalities demonstrated a bicuspid pulmonic valve with doming and poor coaptation of the pulmonic valve leaflets (Figure 1). Additionally, a large patent foramen ovale was visualized in color Doppler (the flap separation = 2 mm and the tunnel length = 11 mm) with bubble passage in agitated saline injection. Bicuspid pulmonic valves constitute a rare finding, and they are most often associated with other congenital heart diseases. Isolated bicuspid pulmonic valves are extremely rare, with an incidence rate of about 0.1% in clinical practice.1 Pulmonary artery aneurysms also comprise a rare abnormality, with an incidence rate of approximately 1 in 14 000 cases in most studies.2 The association between bicuspid pulmonic valves and pulmonary artery aneurysms has been reported, and the pathophysiologic causes of this association include hemodynamic alterations due to bicuspid pulmonic valves and most likely the abnormal migration of neural crest cells.3  The diagnosis of a bicuspid pulmonic valve by 2D imaging is challenging and sometimes impossible. Using 3D echocardiography and reconstruction confers a better assessment of the pulmonic valve morphology and identification of bicuspid pulmonic valves.
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孤立双尖瓣肺动脉动脉瘤1例
一位33岁女性,因甲状腺癌接受甲状腺手术和放射性碘治疗,因用力时呼吸困难而接受超声心动图检查。经胸超声心动图显示左心室大小和功能正常(射血分数= 55%),二尖瓣脱垂伴索赘,轻度二尖瓣反流,三尖瓣主动脉瓣,轻度主动脉不全,轻度三尖瓣反流。最显著的超声心动图表现为中度右心室扩张伴轻度收缩功能障碍,中度右心房扩张,动脉瘤状肺动脉(肺动脉主动脉= 47 mm),轻度肺狭窄(峰值梯度= 22 mmHg),重度肺返流(静脉收缩= 6-7 mm,压力半小时= 105 ms)。经食管超声心动图3D显示双尖肺动脉瓣呈圆顶状,肺动脉瓣小叶的配合不良(图1)。此外,在搅拌盐水注射中,彩色多普勒显示一个大的卵圆孔未闭(瓣距2毫米,隧道长度11毫米),有气泡通道。双尖瓣肺动脉瓣是一种罕见的发现,它们通常与其他先天性心脏病有关。孤立的双尖瓣肺动脉瓣极为罕见,在临床中的发病率约为0.1%肺动脉动脉瘤也是一种罕见的异常,在大多数研究中发病率约为1 / 14000例二尖瓣肺动脉瓣与肺动脉动脉瘤之间的关联已被报道,其病理生理原因包括由二尖瓣肺动脉瓣引起的血流动力学改变和最有可能的神经嵴细胞的异常迁移通过二维成像诊断双尖瓣肺动脉瓣是具有挑战性的,有时是不可能的。使用三维超声心动图和重建可以更好地评估肺动脉瓣形态和识别双尖瓣肺动脉瓣。
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来源期刊
Journal of Tehran University Heart Center
Journal of Tehran University Heart Center Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
46
审稿时长
12 weeks
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