Simmons Ashley, Vacek James, Gupta Kamal
University of Kansas Medical Center, VA Medical Center, Department of Medical Subspecialties, 4801 Linwood Blvd., Kansas City, MO 64128, USA.
J Invasive Cardiol. 2010 Nov;22(11):E176-9.
Dynamic compression of the left main coronary artery during systole is extremely rare. We report a case of a 29-year old female who presented with shortness of breath and chest pain with exertion. She had a history of congenital pulmonic stenosis and had a pulmonary valve resection at age 2. She subsequently developed chronic pulmonic insufficiency. She had normal left ventricular systolic function and a dilated right ventricle with pressure and volume overload diagnosed by echocardiography. She had pulmonary artery hypertension with pulmonary artery pressures noted to be systolic of 62mmHg, diastolic of 10 mmHg, mean of 29 mmHg on right heart catheterization. Her echocardiogram also showed an elevated mean pulmonary artery pressure of 25 mmHg, which was thought to be due to increased flow. On left heart catheterization, she was found to have dynamic systolic compression of the left main coronary artery by a dilated pulmonary artery. This is the first case report of a patient with congenital pulmonic stenosis with a dilated pulmonary trunk causing systolic compression of the left main coronary artery. Dynamic systolic compression of the left main coronary artery is a rare cause of angina, is rarely reported, and requires a high level of suspicion and careful investigation for accurate diagnosis.
左主冠状动脉在收缩期的动态受压极为罕见。我们报告一例29岁女性患者,她在运动时出现呼吸急促和胸痛。她有先天性肺动脉狭窄病史,2岁时接受了肺动脉瓣切除术。随后她出现了慢性肺动脉瓣关闭不全。她的左心室收缩功能正常,经超声心动图诊断为右心室扩张伴压力和容量负荷过重。右心导管检查显示她患有肺动脉高压,肺动脉压力为收缩压62mmHg、舒张压10mmHg、平均压29mmHg。她的超声心动图还显示平均肺动脉压升高至25mmHg,认为是由于血流增加所致。在左心导管检查中,发现她的左主冠状动脉被扩张的肺动脉动态收缩期压迫。这是首例关于先天性肺动脉狭窄伴扩张的肺动脉主干导致左主冠状动脉收缩期受压患者的病例报告。左主冠状动脉动态收缩期受压是心绞痛的罕见病因,鲜有报道,需要高度怀疑并进行仔细检查以准确诊断。