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获得性或先天性心脏病患者不成比例的室间隔增厚的患病率及特征:超声心动图和形态学发现

Prevalence and characteristics of disproportionate ventricular septal thickening in patients with acquired or congenital heart diseases: echocardiographic and morphologic findings.

作者信息

Maron B J, Clark C E, Henry W L, Fukuda T, Edwards J E, Mathews E C, Redwood D R, Epstein S E

出版信息

Circulation. 1977 Mar;55(3):489-96. doi: 10.1161/01.cir.55.3.489.

Abstract

Echocardiographic and necropsy studies were performed in 304 patients with various cardiac diseases. The overall prevalence of disproportionate ventricular septal thickening (septal to free wall ratio greater than or equal to 1.3) was 10%. However, it was related to the type of cardiac lesion. Prevalence was high (greater than 20%) in pulmonary stenosis or primary pulmonary hypertension, lower (less than 15%) in Eisenmenger syndrome or aortic or mitral valvular disease and was not present in atrial or ventricular septal defect. In right ventricular overload, prevalence of disproportionate septal thickening correlated with increasing ventricular systolic pressure. None of 16 patients with disproportionate septal thickening studied at necropsy showed marked disorientation of cardiac muscle cells in the ventricular septum, characteristic of genetically transmitted asymmetric septal hypertrophy (ASH). Furthermore, disproportionate septal thickening was demonstrated by echocardiography in only one of 59 first degree relatives of patients with disproportionate septal thickening and associated cardiac diseases. Thus, disproportionate ventricular septal thickening associated with other cardiac diseases usually is due to secondary hypertrophy and is not a manifestation of genetically transmitted ASH.

摘要

对304例患有各种心脏病的患者进行了超声心动图和尸检研究。不成比例的室间隔增厚(室间隔与游离壁比率大于或等于1.3)的总体患病率为10%。然而,它与心脏病变的类型有关。在肺动脉狭窄或原发性肺动脉高压中患病率较高(大于20%),在艾森曼格综合征或主动脉或二尖瓣瓣膜病中患病率较低(小于15%),而在房间隔或室间隔缺损中不存在。在右心室超负荷时,不成比例的间隔增厚患病率与心室收缩压升高相关。在尸检研究的16例不成比例的间隔增厚患者中,没有一例在室间隔中显示出心肌细胞明显的排列紊乱,这是遗传性不对称性间隔肥厚(ASH)的特征。此外,在不成比例的间隔增厚及相关心脏病患者的59名一级亲属中,只有1人通过超声心动图显示出不成比例的间隔增厚。因此,与其他心脏病相关的不成比例的室间隔增厚通常是由于继发性肥厚,而不是遗传性ASH的表现。

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