Fujita Satoshi, Okamoto Ryuji, Takamura Takeshi, Nakajima Hiroshi, Tanabe Masaki, Nakamori Shiro, Dohi Kaoru, Tanigawa Takashi, Nakamura Mashio, Ito Masaaki
Department of Cardiology and Nephrology, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.
Department of Cardiology, Ise Red Cross Hospital, Ise, Japan.
J Cardiol Cases. 2013 Dec 12;9(1):15-17. doi: 10.1016/j.jccase.2013.08.010. eCollection 2014 Jan.
A 55-year-old man complaining of fever and exertional dyspnea was admitted for coronary angiography to differentiate between fulminant myocarditis and acute coronary syndrome. He had been treated for 17 years for angina pectoris. His electrocardiogram demonstrated ST segment changes in almost all leads. Cardiac catheterization demonstrated severe stenosis in the left descending artery, the diagonal branch, and the right coronary artery. Ultrasonography, however, revealed diffuse hypokinesis of the left ventricle and edematous wall thickening, suggesting fulminant myocarditis. This is the first report in which a patient with fulminant myocarditis with severe coronary artery disease was successfully treated with mechanical cardiopulmonary support, intensive pharmacological therapy, and staged coronary intervention procedures. Complicated coronary artery disease may delay the diagnosis of myocarditis and worsen the clinical outcome. Patients having fulminant myocarditis with coronary artery disease need careful diagnosis, and percutaneous cardiopulmonary support should be considered in the early clinical stage. <: Complicated coronary artery disease may delay the diagnosis of myocarditis and worsen the clinical outcome. It is considered safe to use percutaneous cardiopulmonary support for such patients in the early clinical stage. The present case was rescued with mechanical support in the acute phase of fulminant myocarditis and elective coronary angioplasty in the recovery phase.>.
一名55岁男性,因发热和劳力性呼吸困难入院行冠状动脉造影,以鉴别暴发性心肌炎和急性冠状动脉综合征。他因心绞痛已接受治疗17年。其心电图显示几乎所有导联均有ST段改变。心脏导管检查显示左前降支、对角支和右冠状动脉严重狭窄。然而,超声心动图显示左心室弥漫性运动减弱和室壁水肿增厚,提示暴发性心肌炎。本文首次报道了一名患有严重冠状动脉疾病的暴发性心肌炎患者,通过机械心肺支持、强化药物治疗和分期冠状动脉介入手术成功治愈。复杂的冠状动脉疾病可能会延迟心肌炎的诊断并恶化临床结局。患有暴发性心肌炎合并冠状动脉疾病的患者需要仔细诊断,在临床早期应考虑采用经皮心肺支持。<:复杂的冠状动脉疾病可能会延迟心肌炎的诊断并恶化临床结局。在临床早期对这类患者使用经皮心肺支持被认为是安全的。本病例在暴发性心肌炎急性期通过机械支持及恢复期择期冠状动脉成形术得以救治。>