Hypercholesterolaemic valvulopathy in a young woman with heterozygous familial hypercholesterolaemia.

To cite: Mahajan K, Asotra S, Negi P. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015214254 DESCRIPTION A 19-year-old woman presented with dyspnoea, angina and exertional syncope for the past 1 year. She had an ejection systolic murmur in the aortic area radiating to the carotids. She had multiple skin xanthomas over her feet, knees, hands and buttocks (figure 1). Echocardiography revealed severe calcific aortic stenosis (figure 2). Her serum lowdensity lipoprotein (LDL) was 391 mg/dL, while triglycerides were normal. Her father and brother also had very high LDL levels and a few xanthomas but no features of aortic stenosis. Her mother and two sisters had normal LDL levels. The patient was thus diagnosed as having heterozygous familial hypercholesterolaemia (FH). Coronary angiography revealed plaques in the left anterior descending artery but no significant stenosis (figure 3). The aortic root was severely calcified causing valvular stenosis along with supravalvular stenosis at the sinotubular junction (figure 4 and video 1). The patient underwent successful aortic valve replacement with aortic root enlargement. Histopathological examination of the valve showed lipid deposition and calcification in the aortic cusps. She was put on high-dose statins and ezitimibe post surgery. FH is an autosomal dominant disorder in which the defect lies in the LDL receptor gene. Incidence is approximately 1:500 and 1:1 000 000 in its heterozygous and homozygous forms, respectively. Affected individuals develop early coronary artery disease and severe aortic root calcification, despite optimisation of therapy. Previous studies have demonstrated 2.6–16% prevalence of supravalvular and/or valvular stenosis in patients with heterozygous FH. 3 This case describes an extremely rare presence of both the lesions together in a patient with heterozygous FH with characteristic skin lesions.