Geer J C, Crago C A, Little W C, Gardner L L, Bishop S P
Am J Pathol. 1980 Mar;98(3):663-80.
Morphologic changes in the subendocardial myocardium that appeared to be caused by severe, chronic subendocardial ischemia were studied in patients with fatal ischemic heart disease admitted to the Specialized Center of Research for Ischemic Heart Disease at the University of Alabama in Birmingham in the period 1970--1977. Thirteen patients were selected for this report on the basis that they had the lesions in the subendocardial myocardium we believe to have been caused by subendocardial ischemia and had no evidence of acute or remote myocardial infarction or other conditions that may have contributed to their terminal illness or death. Clinical findings were unstable angina, congestive heart failure, usually no increase in plasma enzymes indicative of myocardial damage, and electrocardiographic changes consistent with subendocardial ischemia. All 13 patients had 75% or greater stenosis of the three major coronary arteries; none had acute thrombotic or embolic coronary artery occlusion. The left ventricle in all cases was hypertrophied. The subendocardial myocardium showed circumferential pallor, hyperemia, or focal fibrosis without perceptible loss of volume in papillary muscles or trabeculae carneae. Microscopically, acute lesions showed one to two layers of preserved myofibers adjacent to the endocardium, vacuolar change in the deeper fibers, and focal areas of coagulation necrosis of variable size in the myocardium external to the fibers with vacuolar change. Coagulation necrosis was extensive in some cases and usually was not associated with infiltration of neutrophils. The repair reaction involved removal of necrotic sarcoplasm by mononuclear phagocytes, resulting in a reticular-appearing tissue without evidence of stromal collapse. Granulation tissue was not seen. Collagen fibers appeared to be deposited within the area of previous sarcolemmal sheaths. The distribution and morphology of subendocardial myocardial lesions associated with severe coronary atherosclerosis are distinctive and can be distinguished from myocardial necrosis or fibrosis associated with acute total occlusion of a coronary artery.
1970年至1977年期间,在阿拉巴马大学伯明翰分校缺血性心脏病专门研究中心收治的致命性缺血性心脏病患者中,对似乎由严重慢性心内膜下缺血引起的心内膜下心肌形态学变化进行了研究。选择了13例患者纳入本报告,依据是他们的心内膜下心肌有我们认为由心内膜下缺血引起的病变,且无急性或陈旧性心肌梗死或其他可能导致其终末期疾病或死亡的情况。临床发现为不稳定型心绞痛、充血性心力衰竭,通常血浆中提示心肌损伤的酶无升高,且心电图变化与心内膜下缺血一致。所有13例患者三大冠状动脉狭窄均达75%或更高;无一例有急性血栓形成或栓塞性冠状动脉闭塞。所有病例左心室均肥厚。心内膜下心肌呈现环形苍白、充血或局灶性纤维化,乳头肌或肉柱无明显体积减小。显微镜下,急性病变显示心内膜相邻处有一至两层保存的肌纤维,较深层纤维有空泡样改变,在有空泡样改变的纤维外部心肌中有大小不一的局灶性凝固性坏死区。凝固性坏死在某些病例中广泛存在,通常与中性粒细胞浸润无关。修复反应包括单核吞噬细胞清除坏死的肌浆,形成网状组织,无基质塌陷迹象。未见肉芽组织。胶原纤维似乎沉积在先前肌膜鞘所在区域内。与严重冠状动脉粥样硬化相关的心内膜下心肌病变的分布和形态具有特征性,可与冠状动脉急性完全闭塞相关的心肌坏死或纤维化相鉴别。