Division of Cardiovascular Surgery, Mayo Clinic, Rochester, Minnesota 55905, USA.
Ann Thorac Surg. 2011 Apr;91(4):1263-5. doi: 10.1016/j.athoracsur.2010.09.041.
Midventricular hypertrophic cardiomyopathy is a rare form of cardiomyopathy that may be associated with an apical aneurysm. The mechanism of aneurysm formation is uncertain, but it may be related to subendocardial ischemia. In this report, we describe a 57-year-old man with recurrent ventricular arrhythmias that were refractory to medical treatment because of midventricular hypertrophic cardiomyopathy and apical aneurysm. He was treated successfully with apical aneurysmectomy, myectomy, and subendocardial resection. Six months postoperatively, the patient was free of symptoms and was taken off all anti-arrhythmic medications with one inappropriate discharge from the implantable cardioverter-defibrillator at 4 months.
室间隔中部肥厚型心肌病是一种罕见的心肌病,可能与心尖部瘤有关。动脉瘤形成的机制尚不确定,但可能与心内膜下缺血有关。本报告描述了 1 例 57 岁男性,因室间隔中部肥厚型心肌病和心尖部瘤导致反复出现室性心律失常,且对药物治疗无效。他成功地接受了心尖部瘤切除术、心肌切除术和心内膜下切除术治疗。术后 6 个月,患者症状消失,停用所有抗心律失常药物,植入式心律转复除颤器在 4 个月时出现 1 次非恰当放电。