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二尖瓣脱垂。发病机制研究。

The floppy mitral valve. Study on pathogenesis.

作者信息

Olsen E G, Al-Rufaie H K

出版信息

Br Heart J. 1980 Dec;44(6):674-83. doi: 10.1136/hrt.44.6.674.

Abstract

The pathogenesis of the floppy valve syndrome is not fully solved. An almost invariable histological finding is the great accumulation of mucinous material in the valve leaflets and constitutes the basis of the valvular theory of the syndrome. The presence of a mucinous layer in normal valves-- the zona spongiosa--is not well recognised. To establish the normal range of the extent of this zone, 50 excised mitral valves from patients aged 2 to 89 years and who died as a result of road traffic accidents or non-cardiac causes have been analysed by measuring the thickness of the zone in relation to the valve thickness. A range of 0 to 60 per cent was found and this was not influenced by age. The findings were compared with 50 patients clinically diagnosed as suffering from the floppy valve syndrome. A value of over 60 per cent (range 62 to 94%) was found in 43 patients. The increase in the extent of the mucinous material was considered to be a secondary change in the thickened fibrosa which normally accompanies the floppy valve syndrome. Measurements of zona spongiosa falling within the normal range were found in seven patients. The clinical features, complications, and accompanying conditions have also been analysed. Chordal rupture had occurred in 20 patients, infective endocarditis in three, and calcification was found in four valves. In four patients the aortic valve was also involved and accompanying aortic root dilatation in an additional patient. It is suggested that these patients should not be included in the group of Marfan's forme fruste, nor in the typical floppy mitral valve syndrome. Apart from the valvular theory, the myocardial theory in the pathogenesis of the syndrome has been discussed and the components ensuring normal mitral valve function have been reviewed. It is concluded that an inherent, prominent zona spongiosa predisposes to the floppy valve syndrome, particularly if any one of the components of normal valve function is abnormal.

摘要

瓣膜松弛综合征的发病机制尚未完全阐明。一个几乎恒定不变的组织学发现是瓣叶中有大量黏液样物质积聚,这构成了该综合征瓣膜学说的基础。正常瓣膜中存在黏液层——海绵层,这一点尚未得到充分认识。为确定该区域范围的正常界限,对50例年龄在2至89岁、因交通事故或非心脏原因死亡的患者切除的二尖瓣进行了分析,通过测量该区域厚度与瓣膜厚度的关系来进行分析。结果发现该区域范围为0至60%,且不受年龄影响。将这些结果与50例临床诊断为瓣膜松弛综合征的患者进行了比较。43例患者该区域值超过60%(范围为62%至94%)。黏液样物质范围的增加被认为是增厚的纤维层的继发性改变,而增厚的纤维层通常伴随瓣膜松弛综合征出现。7例患者的海绵层测量值在正常范围内。还对临床特征、并发症及伴随情况进行了分析。20例患者发生腱索断裂,3例发生感染性心内膜炎,4个瓣膜发现钙化。4例患者主动脉瓣也受累,另有1例患者伴有主动脉根部扩张。有人提出,这些患者不应归入马方综合征顿挫型组,也不应归入典型的二尖瓣松弛综合征组。除了瓣膜学说外,还讨论了该综合征发病机制中的心肌学说,并对确保二尖瓣正常功能的组成部分进行了综述。得出的结论是,固有且突出的海绵层易引发瓣膜松弛综合征,特别是在正常瓣膜功能的任何一个组成部分异常的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c74/482465/c0ba7e5d8f4e/brheartj00202-0067-a.jpg

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