Ando M, Takao A
Heart Vessels. 1986;2(2):117-26. doi: 10.1007/BF02059966.
In an attempt to clarify the pathogenetic morphology of aortic regurgitation (AR) due to prolapse of the aortic valve (prolapsing AR) associated with ventricular septal defect (VSD), 201 specimens from Japanese autopsy series with isolated VSD were examined. Among these hearts, there were 128 cases (64%) of infundibular VSD (IVSD); 29 of them (14%) showed AR due to prolapsed cusp, of which nine cases developed a large aneurysm of the sinus of Valsalva. Another 32 cases (16%) had varying degrees of prolapse but without AR and were considered to show the prodrome of prolapsing AR. These 61 cases (30%) were examined with special reference to the type of septal alignment, location of the defect, relation of the defect to the aortic valve, and anomalies of the aortic valve and sinus of Valsalva. There were two principal forms in this syndrome: The common form, i.e., simple punched-hole IVSD with normal septal alignment in 82% (50/61) of cases, and a rare form, i.e., malalignment IVSD in 18% (11/61) of cases. The latter included Eisenmenger-type IVSD due to anteriorly deviated outlet septum (10/11 cases) and coarctation-type IVSD due to posteriorly deviated septum (1/11). Both forms had several subtypes according to the location of the defect, i.e., subpulmonic, muscular, perimembranous, and total IVSD. The relevant anatomical findings of the common form of the syndrome were: There was no septal malalignment with a normal aortic valve position. The VSD was a simple muscular defect in any part of the infundibular septum between the pulmonary valve above and the membranous septum below, the majority of cases (80%), however, showed subpulmonic IVSD. The annulus and sinus of Valsalva wall of the right coronary cusp, which is normally supported firmly by this septum, became exposed in the muscle defect and were poorly supported. The majority of cases showed a normally formed aortic valve but with poor support. The muscular defect was relatively large, but the functioning VSD was usually less than moderate in size with a half-moon shape below the denuded sinus of Valsalva wall and annulus. The functioning VSD appeared to become narrower depending on the degree of prolapse into the defect, resulting in a crescent-moon or slit-like shape, and it may close in rare cases. The major anatomical findings of the rare form were: There was mild to moderate dextroposition (or levoposition) of the aortic valve due to a septal malalignment.(ABSTRACT TRUNCATED AT 400 WORDS)
为了阐明与室间隔缺损(VSD)相关的主动脉瓣脱垂所致主动脉反流(AR)(脱垂性AR)的发病机制形态学,对来自日本尸检系列的201例孤立性VSD标本进行了检查。在这些心脏中,有128例(64%)为漏斗部室间隔缺损(IVSD);其中29例(14%)因瓣叶脱垂出现AR,其中9例形成了巨大的主动脉窦瘤。另外32例(16%)有不同程度的脱垂但无AR,被认为是脱垂性AR的前驱表现。对这61例(30%)病例特别参照了室间隔排列类型、缺损位置、缺损与主动脉瓣的关系以及主动脉瓣和主动脉窦的异常情况进行了检查。该综合征有两种主要形式:常见形式,即82%(50/61)的病例为单纯穿孔性IVSD且室间隔排列正常;罕见形式,即18%(11/61)的病例为对位不齐性IVSD。后者包括由于出口间隔向前移位导致的艾森曼格型IVSD(10/11例)和由于间隔向后移位导致的缩窄型IVSD(1/11例)。根据缺损位置,两种形式都有几种亚型,即肺动脉瓣下型、肌部型、膜周型和完全型IVSD。该综合征常见形式的相关解剖学发现为:主动脉瓣位置正常,无室间隔对位不齐。VSD是位于上方肺动脉瓣和下方膜性间隔之间的漏斗部间隔任何部位的单纯肌性缺损,然而,大多数病例(80%)表现为肺动脉瓣下IVSD。正常情况下由该间隔牢固支撑的右冠状动脉瓣叶的瓣环和主动脉窦壁在肌性缺损处暴露,支撑不良。大多数病例主动脉瓣形态正常但支撑不佳。肌性缺损相对较大,但功能性VSD通常大小小于中度,呈半月形位于裸露的主动脉窦壁和瓣环下方。功能性VSD似乎会根据脱垂至缺损的程度而变窄,导致呈新月形或裂隙状,在罕见情况下可能会闭合。罕见形式的主要解剖学发现为:由于室间隔对位不齐,主动脉瓣有轻度至中度右移(或左移)。(摘要截断于400字)