Bharati S, Lev M
J Thorac Cardiovasc Surg. 1984 Jul;88(1):97-101.
The surgical anatomy of 230 hearts with hypoplasia of the aortic tract complex or the hypoplastic left heart syndrome is described in detail. Recent work has indicated that this may be an operable entity. There were 105 hearts with aortic atresia and mitral stenosis, 95 hearts with aortic and mitral atresia, and 30 hearts with severe aortic and mitral stenosis. Special emphasis is given to the right atrium, right ventricle, and sizes of the ascending and transverse aorta. Attention is called to the pathological changes in the tricuspid orifice and valve and in the ventricular septum. It was of interest that many of the hearts had only a patent foramen ovale rather than a distinct atrial septal defect. In addition, the atrial septum was abnormally formed. The anatomic data presented may be of surgical import. Hypoplasia of the aortic tract complexes may be variations of premature narrowing of foramen ovale.
详细描述了230例具有主动脉道复合体发育不全或左心发育不全综合征的心脏的手术解剖结构。近期研究表明,这可能是一种可手术治疗的病症。其中有105例心脏为主动脉闭锁合并二尖瓣狭窄,95例心脏为主动脉和二尖瓣闭锁,30例心脏为严重主动脉和二尖瓣狭窄。特别强调了右心房、右心室以及升主动脉和横主动脉的大小。还提到了三尖瓣口和瓣膜以及室间隔的病理变化。有趣的是,许多心脏仅有卵圆孔未闭而非明显的房间隔缺损。此外,房间隔形成异常。所呈现的解剖学数据可能具有手术意义。主动脉道复合体发育不全可能是卵圆孔过早狭窄的变异情况。