Congenital Heart Disease Division, Department of Cardiology and Vascular Medicine, University of Padjadjaran, Hasan Sadikin General Hospital, Jl. Pasteur No. 38, Bandung, 40161, Indonesia.
Department of Cardiology and Vascular Medicine, University of Padjadjaran, Hasan Sadikin General Hospital, Bandung, Indonesia.
BMC Cardiovasc Disord. 2022 Mar 5;22(1):89. doi: 10.1186/s12872-022-02524-w.
Left main coronary artery disease secondary to pulmonary artery compression related to Eisenmenger syndrome is an under-suspected condition that can cause fatal outcomes if left untreated. It presents with typical angina but is frequently mistaken for pulmonary hypertension (PH) symptoms. It is now recognized as one of the few important causes of angina in PH.
A 37-year-old man with a history of unoperated atrial septal defect and Eisenmenger syndrome came to the outpatient department with a chief complaint of angina on exertion. Electrocardiogram showed regular sinus rhythm with right axis deviation, right ventricular hypertrophy, deep T-wave inversion in inferior and anterior leads suggestive of ischemia or strain, and incomplete right bundle branch block. Cardiac CT showed compression of the left main coronary artery due to a dilated main pulmonary artery. Therefore, this patient was diagnosed with Eisenmenger syndrome with left main compression due to dilated pulmonary artery. He was treated successfully with IVUS-guided stent implantation. The patient experienced marked improvement in regular activities, with no recurrence of angina symptoms. Angiography 3 months after the procedure revealed good patency of the stent, without significant stenosis.
Left main coronary artery compression is a complication that should be suspected in patients with Eisenmenger syndrome presenting with angina symptoms. Non-invasive modalities are recommended for diagnostic evaluation, but the gold-standard technique remains coronary angiography. The best treatment is not well-established, with either myocardial revascularization or PH treatment, but a left main coronary artery stenting procedure is considered an ideal emergent treatment to provide a better quality of life for patients in this condition.
继发于艾森曼格综合征的肺动脉压迫导致的左主干冠状动脉疾病是一种被低估的疾病,如果不进行治疗可能会导致致命后果。它表现为典型的心绞痛,但常被误诊为肺动脉高压(PH)症状。现在它被认为是 PH 中少数几种重要的心绞痛原因之一。
一名 37 岁男性,患有未手术的房间隔缺损和艾森曼格综合征,因劳力性心绞痛就诊于门诊。心电图显示窦性心律,电轴右偏,右心室肥厚,下壁和前壁导联的深 T 波倒置提示缺血或劳损,以及不完全性右束支传导阻滞。心脏 CT 显示由于主肺动脉扩张导致左主干冠状动脉受压。因此,该患者被诊断为艾森曼格综合征伴左主干因肺动脉扩张所致的受压。他成功地接受了 IVUS 引导下的支架植入术治疗。患者在日常活动中明显改善,心绞痛症状未再复发。术后 3 个月的血管造影显示支架通畅良好,无明显狭窄。
左主干冠状动脉受压是艾森曼格综合征患者出现心绞痛症状时应怀疑的一种并发症。推荐使用非侵入性方法进行诊断评估,但冠状动脉造影仍然是金标准技术。最佳治疗方法尚未确定,心肌血运重建或 PH 治疗均可,但左主干冠状动脉支架置入术被认为是这种情况下的理想紧急治疗方法,可以为患者提供更好的生活质量。