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先天性心脏病的肺活检:肺血管疾病的形态计量学研究方法

Lung biopsy in congenital heart disease: a morphometric approach to pulmonary vascular disease.

作者信息

Rabinovitch M, Haworth S G, Castaneda A R, Nadas A S, Reid L M

出版信息

Circulation. 1978 Dec;58(6):1107-22. doi: 10.1161/01.cir.58.6.1107.

Abstract

Fifty patients with congenital heart disease, ages 2 days-30 years (median 12 months) at cardiac surgery, underwent lung biopsy to assess pulmonary vascular disease (PVD). Twenty-six had ventricular septal defects (VSD), 17 d-transposition of the great arteries (D-TGA), and seven, defects of the atrioventricular canal (AVC). Quantitative morphologic data was correlated with hemodynamic data. Three new grades of PVD were observed. Abnormal extension of muscle into peripheral arteries (grade A) was found in all patients; all had increased pulmonary blood flow. In addition, 38 of 50 patients had an increase in percentage arterial wall thickness (grade B); this correlated with elevation in pulmonary artery (PA) pressure (r = 0.59). Another 10 of 50 patients had, in addition to A and B, a reduction in the number of small arteries (grade C); nine of 10 were patients with elevated PA resistance greater than 3.5 mu/m2 (P less than 0.005). All three patients with Heath-Edwards changes of grade III or worse also had grade C. Reduction in peripheral arterial number probably precedes obliterative PVD and may identify those patients in whom, despite corrective surgery, PVD will progress.

摘要

50例先天性心脏病患者,心脏手术时年龄为2天至30岁(中位年龄12个月),接受了肺活检以评估肺血管疾病(PVD)。其中26例患有室间隔缺损(VSD),17例患有大动脉d型转位(D-TGA),7例患有房室通道缺损(AVC)。定量形态学数据与血流动力学数据相关。观察到三种新的PVD分级。所有患者均发现肌肉异常延伸至外周动脉(A级);所有患者肺血流量均增加。此外,50例患者中有38例动脉壁厚度百分比增加(B级);这与肺动脉(PA)压力升高相关(r = 0.59)。50例患者中的另外10例,除了A级和B级外,小动脉数量减少(C级);10例中有9例是PA阻力大于3.5 mu/m2的患者(P < 0.005)。所有3例希思-爱德华兹分级为III级或更严重的患者也有C级。外周动脉数量减少可能先于闭塞性PVD出现,并且可能识别出那些尽管接受了矫正手术但PVD仍会进展的患者。

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