Glancy D L, Roberts W C
Cathet Cardiovasc Diagn. 1976;2(3):215-52. doi: 10.1002/ccd.1810020302.
The clinical, laboratory, and morphologic features of congenitally obstructive lesions causing pulmonary venous hypertension are reviewed. These lesions are responsible for considerable infant mortality and morbidity, especially in the first weeks of life, are not infrequently encountered in older children, and are occasionally seen in adults. The presence of a malformation causing pulmonary venous hypertension often can be detected clinically, but precise anatomical and physiological diagnoses, usually necessary for optimal patient management, often can be made only by detailed laboratory study. Cardiac catheterization and angiocardiography remain the prime modes of accurate diagnosis in such patients, many of whom have other significant cardiovascular malformations, and echocardiography is an extremely useful adjunct, especially in patients with mitral valvular stenosis, hypoplasia, or atresia. The only definitive treatment in any of these patients is operative relief of the obstruction, and the chances of success depend not only on the skill of the surgeon, but also on the nature of the obstructing lesion, the types of associated malformations, and the precision with which these are defined preoperatively.
本文回顾了导致肺静脉高压的先天性阻塞性病变的临床、实验室及形态学特征。这些病变导致了相当高的婴儿死亡率和发病率,尤其是在出生后的头几周,在大龄儿童中也不少见,偶尔也可见于成人。导致肺静脉高压的畸形通常可通过临床检查发现,但精确的解剖学和生理学诊断(这通常是实现最佳患者管理所必需的)往往只能通过详细的实验室研究才能做出。心导管检查和心血管造影仍然是此类患者准确诊断的主要方法,其中许多患者还伴有其他严重的心血管畸形,而超声心动图是一种极其有用的辅助手段,尤其适用于二尖瓣狭窄、发育不全或闭锁的患者。这些患者唯一确定的治疗方法是通过手术解除梗阻,成功的几率不仅取决于外科医生的技术,还取决于梗阻病变的性质、相关畸形的类型以及术前对这些畸形的明确程度。