Sitosterolemia Presenting With Severe Hypercholesterolemia and Intertriginous Xanthomas in a Breastfed Infant: Case Report and Brief Review
Authors:
- 1 May 2014
- journal article
- case report
- Published by The Endocrine Society in The Journal of Clinical Endocrinology & Metabolism
- Vol. 99 (5) , 1512-1518
Abstract
Sitosterolemia is an autosomal recessive disorder characterized by increased intestinal absorption of plant sterols. It is caused by mutations in genes encoding ATP-binding cassette, subfamily G5 (ABCG5) or G8 (ABCG8), and clinical features include elevated plant sterol levels, xanthomas, and accelerated atherosclerosis. Although it was originally reported in patients with normolipemic xanthomas, patients with sitosterolemia also hyperabsorb cholesterol, and serum cholesterol levels tend to be elevated. We report an infant with sitosterolemia who presented with severe hypercholesterolemia and intertriginous xanthomas. A 15-month-old Korean girl presented with yellow dermal plaques over flexural areas including the wrist, neck, and gluteal folds, which were consistent with intertriginous xanthomas. The lesions were first noticed at 3 months of age when she was being exclusively breastfed. Her total cholesterol and low-density lipoprotein-cholesterol levels were 675 and 540 mg/dL, respectively. A low-fat/low-cholesterol diet and cholestyramine therapy were introduced. Unexpectedly, her serum cholesterol level decreased dramatically and normalized in 2 months. Cholestyramine was tapered off. The xanthomas also regressed and disappeared by 3 years of age. Gas chromatography-mass spectrometric analysis was performed with serum drawn at 3 years of age when her low-density lipoprotein-cholesterol was 118 mg/dL, which revealed striking elevation of her sitosterol level at 19.36 mg/dL. Direct sequencing for ABCG5 revealed compound heterozygous null mutations c.904+1G>A (p.Met302Asnfs*82) and c.1336C>T(p.Arg446*). Our case suggests that sitosterolemia can present with severe hypercholesterolemia and intertriginous xanthomas. Sitosterolemia should be suspected when a patient with hypercholesterolemia shows unexpectedly good response to dietary modification or bile acid sequestrant therapy.Keywords
This publication has 28 references indexed in Scilit:
- Phytosterols and phytosterolemia: gene–diet interactionsGenes & Nutrition, 2010
- Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemiaHuman Molecular Genetics, 2010
- Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and childrenJournal of Inherited Metabolic Disease, 2010
- Long-term efficacy and safety of ezetimibe 10 mg in patients with homozygous sitosterolemia: a 2-year, open-label extension studyInternational Journal Of Clinical Practice, 2008
- Familial Homozygous Hypercholesterolemia: Report of Two Patients and Review of the LiteraturePediatric Dermatology, 2007
- No Association Between Plasma Levels of Plant Sterols and Atherosclerosis in Mice and MenArteriosclerosis, Thrombosis, and Vascular Biology, 2004
- A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemiaHuman Genetics, 2004
- Intertriginous xanthomas: a marker of homozygous type IIa hyperlipoprotinemiaInternational Journal of Dermatology, 2004
- Abnormal metabolism of shellfish sterols in a patient with sitosterolemia and xanthomatosis.Journal of Clinical Investigation, 1986
- Phytosterolaemia, xanthomatosis and premature atherosclerotic arterial disease: a case with high plant sterol absorption, impaired sterol elimination and low cholesterol synthesisEuropean Journal of Clinical Investigation, 1980