Hashimoto R, Miyamura H, Eguchi S
Br Heart J. 1984 Mar;51(3):358-60. doi: 10.1136/hrt.51.3.358.
After follow up for seven years a 10 year old boy with congenital aortic regurgitation was found to have a tricuspid non-stenotic aortic valve at operation. The right coronary cusp was dysplastic, thickened, and contracted; the gap between its free margin and aortic wall was bridged with two fibrous bands; and the left coronary and non-coronary cusps were almost normal. The aortic valve was replaced with a prosthesis (St Jude Medical No 23), and the postoperative course was uneventful.
对一名患有先天性主动脉瓣反流的10岁男孩进行了7年的随访后,手术发现其有一个三尖瓣无狭窄的主动脉瓣。右冠状动脉瓣发育不良、增厚并收缩;其游离缘与主动脉壁之间的间隙被两条纤维带桥接;左冠状动脉瓣和无冠状动脉瓣几乎正常。用人工瓣膜(圣犹达医疗23号)替换了主动脉瓣,术后过程顺利。