Severe supravalvar aortic stenosis in familial homozygous hypercholesterolemia

被引:8
作者
Arora, G
Fraser, CD
Kearney, DL
Vincent, JA
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Lillie Frank Abercrombie Sect Pediat Cardiol, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Div Congenital Heart Surg, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[4] Arizona Pediat Cardiol Consultants, Phoenix, AZ 85006 USA
关键词
hypercholesterolemia; aortic stenosis; cardiac surgery; familial hyperlipidemia; congenital dyslipidemia;
D O I
10.1007/s00246-005-5809-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Familial homozygous hypercholesterolemia is a rare disease with diverse clinical presentations. Patients often present with cutaneous xanthomas, particularly in the Achilles' tendon. They may have significant cardiovascular involvement, including premature atherosclerotic coronary artery disease and valvar and supravalvar aortic stenosis. Standard therapy includes diet modulation, pharmacotherapy, and lipid apheresis. Rarely, patients require surgical intervention for coronary artery bypass grafting and/or relief of the aortic stenosis. We present the case of a patient with severe progressive supravalvar aortic stenosis that ultimately required surgical resection despite aggressive medical therapy.
引用
收藏
页码:282 / 285
页数:4
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