Kim Y M, Yoo S J, Choi J Y, Kim S H, Bae E J, Lee Y T
Department of Radiology, Sejong Heart Institute, Korea.
Cardiol Young. 1999 Jan;9(1):37-41. doi: 10.1017/s1047951100007356.
We investigated the catheterization and angiographic findings of 26 patients with Williams' syndrome to evaluate the natural course of supravalvar aortic stenosis and peripheral pulmonary arterial stenosis. The severity of the stenosis was correlated with age and body surface area in terms of the pulmonary arterial index, right ventricular systolic pressure, sinutubular ratio (ratio of measured to mean normal diameter of sinutubular junction), and systolic pressure gradient across the sinutubular junction. In patients with pulmonary arterial stenosis (n=20), right ventricular systolic pressure tended to decrease, and pulmonary arterial index increased, with increase in age and body surface area. Between the groups with and without pulmonary arterial stenosis, there was significant difference in age (mean 4.70 vs. 9.87, p=0.019), body surface area (0.62 vs. 1.16, p=0.002), pulmonary arterial index (152 vs. 317, p=0.002) and right ventricular systolic pressure (73.9 vs. 33.0, p=0.006). As all patients showed similar diameters at the sinutubular junction regardless of age and body size, sinutubular ratio decreased with increases in age and body surface area. The group with abnormal coronary arteries (n=7) had smaller sinutubular ratio (0.46 vs. 0.61, p=0.021) and higher pressure gradients between the left ventricle and the aorta (67.6 vs. 42.2, p=0.023) than did the group with normal coronary arteries. Stenosis of a coronary artery, or a branch of the aortic arch, was observed only in three patients with diffuse aortic stenosis. Our results suggest that, with time, peripheral pulmonary arterial stenosis tends to improve, and supravalvar aortic stenosis to progress. Failure of growth of the sinutubular junction might be responsible for the progression of the aortic lesion. Progression of the aortic lesion may be associated with involvement of the coronary arteries.
我们研究了26例威廉姆斯综合征患者的导管插入术和血管造影结果,以评估瓣上主动脉狭窄和外周肺动脉狭窄的自然病程。就肺动脉指数、右心室收缩压、窦管比(测量的窦管交界处直径与正常平均直径之比)以及跨窦管交界处的收缩压梯度而言,狭窄的严重程度与年龄和体表面积相关。在患有肺动脉狭窄的患者(n = 20)中,随着年龄和体表面积的增加,右心室收缩压趋于降低,肺动脉指数增加。在有和没有肺动脉狭窄的两组之间,年龄(平均4.70对9.87,p = 0.019)、体表面积(0.62对1.16,p = 0.002)、肺动脉指数(152对317,p = 0.002)和右心室收缩压(73.9对33.0,p = 0.006)存在显著差异。由于所有患者无论年龄和体型如何,在窦管交界处均显示相似的直径,因此窦管比随着年龄和体表面积的增加而降低。冠状动脉异常的组(n = 7)比冠状动脉正常的组具有更小的窦管比(0.46对0.61,p = 0.021)和更高的左心室与主动脉之间的压力梯度(67.6对42.2,p = 0.023)。仅在3例弥漫性主动脉狭窄患者中观察到冠状动脉或主动脉弓分支的狭窄。我们的结果表明,随着时间的推移,外周肺动脉狭窄趋于改善,而瓣上主动脉狭窄趋于进展。窦管交界处生长失败可能是主动脉病变进展的原因。主动脉病变的进展可能与冠状动脉受累有关。