老年人扩张型心肌病的临床病理研究

Journal of cardiography. Supplement Pub Date : 1986-01-01
S Ohkawa, J Inoue, M Sugiura
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引用次数: 0

摘要

未标记:这是一项在3000例60岁或以上的连续尸检病例中对7例扩张型心肌病(DCM)进行的临床病理研究报告。在本研究中,老年人DCM定义为:1)临床和病理检查显示原因不明的心脏明显扩大的难治性心力衰竭,不包括高血压心脏病、缺血性心脏病和瓣膜性心脏病;2)病理检查显示心脏重量大于400 g,冠状动脉正常,冠状动脉狭窄指数(CSI)小于9/15,心脏呈球状,左心室明显扩张。结果:老年DCM 7例,男2例,女5例,平均年龄69.7岁。发病率为0.23%(7/ 3000例)。这组患者的平均年龄小于其他心脏疾病如心肌梗死或瓣膜病的老年人。临床表现:临床病程3 ~ 22年,平均12年。7例中有3例的症状一直持续到中年。心电图显示房颤5例(71%),左束支传导阻滞3例(43%),完全性心脏传导阻滞1例(14%)。平均心胸比例为77.3%。瓣膜返流5例,其中二尖瓣返流5例,三尖瓣返流3例。所有患者均死于心脏事件。病理表现:心脏重量410 ~ 600 g,平均527 g, CSI 1/15 ~ 8/15,平均4.4/15。虽然有5例瓣膜返流,但相应瓣膜未见原发性改变。因此,这些病例的瓣膜反流是由于瓣膜环扩张和/或相关的心室壁顺应性降低引起的继发性改变。房室瓣环周长增大,但半月瓣环在正常范围内。形态学计算的双侧心房和心室容积较大[分别为201 ml(正常77 ml)和83 ml(正常29 ml)]。3例有附壁血栓,2例发生肺梗死。组织学上,纤维化为主型3例,肥厚为主型2例,变性为主1例,混合型1例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A clinicopathologic study of dilated cardiomyopathy in the aged].

Unlabelled: This is a report of a clinicopathologic study of seven cases with dilated cardiomyopathy (DCM) among 3,000 consecutive autopsied cases 60 years or more in age. In this study DCM in the aged was defined as 1) cases of refractory heart failure with marked cardiomegaly of unknown cause by clinical and pathologic examinations, excluding hypertensive heart disease, ischemic heart disease, and valvular heart disease, and 2) pathologic examinations showing cardiac weight more than 400 g, normal coronary arteries with less than 9/15 coronary stenotic index (CSI) and a globular shaped heart with marked dilatation of the left ventricle. The following results were obtained: Seven cases of DCM in the aged consisted of two men and five women with an average age of 69.7 years. The incidence was 0.23% (7/3,000 autopsies). The average age of this group was less than those with other heart diseases such as myocardial infarction or valvular disease in the aged.

Clinical findings: The clinical course ranged from 3 to 22 years with a mean of 12 years. The symptoms of three of the seven cases persisted from the middle age. Electrocardiograms showed atrial fibrillation in five cases (71%), left bundle branch block in three (43%) and complete heart block in one (14%). The mean cardiothoracic ratio was 77.3%. Valvular regurgitation was detected in five cases including five with mitral regurgitation (MR) and three with tricuspid regurgitation (TR). All patients died of cardiac events. Pathologic findings: The heart weights ranged from 410 g to 600 g, with an average of 527 g, and a CSI from 1/15 to 8/15 with a mean of 4.4/15. Though five cases had valvular regurgitation, no primary change was observed in the corresponding valves. Therefore, the valvular regurgitation in these cases were attributed to secondary changes due to dilatation of the valve ring and/or associated decreased compliance of the ventricular wall. The circumferences of the atrioventricular valve rings were enlarged, but the semilunar valve rings were in normal range. Bilateral atrial and ventricular volumes calculated morphologically were larger [201 ml (normal 77 ml) and 83 ml (normal 29 ml), respectively]. Three cases had mural thrombi, two of whom developed pulmonary infarction. Histologically, there were three cases with the fibrosis dominant type, two with the hypertrophy dominant type, one with the degenerative type, and one of the mixed type, respectively.

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