Dec G W, Waldman H, Southern J, Fallon J T, Hutter A M, Palacios I
Cardiac Unit, Massachusetts General Hospital, Boston 02114.
J Am Coll Cardiol. 1992 Jul;20(1):85-9. doi: 10.1016/0735-1097(92)90141-9.
Anecdotal reports have shown that myocarditis can mimic acute myocardial infarction with chest pain, electrocardiographic (ECG) abnormalities, serum creatine kinase elevation and hemodynamic instability. Thirty-four patients with clinical signs and symptoms consistent with acute myocardial infarction underwent right ventricular endomyocardial biopsy during a 6.5-year period after angiographic identification of normal coronary anatomy. Myocarditis was found on histologic study in 11 of these 34 patients. Cardiogenic shock requiring intraaortic balloon support developed within 6 h of admission in three (27%) of the patients with myocarditis. The mean age of the group with myocarditis was 42 +/- 5 years. A preceding viral illness had been present in six patients (54%). The ECG abnormalities were varied and included ST segment elevation (n = 6), T wave inversions (n = 3), ST segment depression (n = 2) and pathologic Q waves (n = 2). The ECG abnormalities were typically seen in the anterior precordial leads but were diffusely evident in three patients. Left ventricular function was normal in six patients and globally decreased in the remaining five patients, whose ejection fraction ranged from 14% to 45%. Lymphocytic myocarditis was diagnosed in 10 patients, and giant cell myocarditis was detected in the remaining patient. Four patients with impaired left ventricular function received immunosuppressive therapy with prednisone and either azathioprine (n = 2) or cyclosporine (n = 2). All six patients whose left ventricular function was normal on admission remain alive in functional class I. Of the five patients with impaired systolic function, ejection fraction normalized in three of the four patients who received immunosuppressive therapy within 3 months of treatment and in the one patient who received only supportive therapy.(ABSTRACT TRUNCATED AT 250 WORDS)
轶事报道显示,心肌炎可表现为胸痛、心电图(ECG)异常、血清肌酸激酶升高及血流动力学不稳定,酷似急性心肌梗死。34例临床症状和体征与急性心肌梗死相符的患者,在血管造影显示冠状动脉解剖结构正常后的6.5年期间接受了右心室心内膜活检。这34例患者中,组织学研究发现11例患有心肌炎。3例(27%)心肌炎患者在入院后6小时内发生需要主动脉内球囊支持的心源性休克。心肌炎组患者的平均年龄为42±5岁。6例患者(54%)此前有病毒感染病史。心电图异常多样,包括ST段抬高(n = 6)、T波倒置(n = 3)、ST段压低(n = 2)及病理性Q波(n = 2)。心电图异常通常见于胸前导联,但3例患者广泛存在。6例患者左心室功能正常,其余5例患者左心室功能整体下降,射血分数在14%至45%之间。10例患者诊断为淋巴细胞性心肌炎,其余1例患者检测出巨细胞性心肌炎。4例左心室功能受损的患者接受了泼尼松联合硫唑嘌呤(n = 2)或环孢素(n = 2)的免疫抑制治疗。入院时左心室功能正常的6例患者均存活,心功能为I级。5例收缩功能受损的患者中,4例接受免疫抑制治疗的患者中有3例在治疗后3个月内射血分数恢复正常,1例仅接受支持治疗的患者射血分数也恢复正常。(摘要截选至250词)