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Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.

Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.

期刊: WMJ : official publication of the State Medical Society of Wisconsin 日期: 2026-01-01 PMID: 42623630 浏览: 8
作者: Beacher D, Ott A, Plier R
D, B., A, O., & R, P. (2026). Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.. WMJ : official publication of the State Medical Society of Wisconsin.
D B, A O, R P. Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.. WMJ : official publication of the State Medical Society of Wisconsin. 2026; PMID: 42623630
D B, A O, R P. Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.[J]. WMJ : official publication of the State Medical Society of Wisconsin. 2026.
@article{d2026,
  author = {Beacher D and Ott A and Plier R},
  title = {Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.},
  journal = {WMJ : official publication of the State Medical Society of Wisconsin},
  year = {2026},
  note = {PMID: 42623630},
}
TY  - JOUR
AU  - Beacher D
AU  - Ott A
AU  - Plier R
TI  - Sitosterolemia: A Rare Cause of Severe Hypercholesterolemia in Children.
T2  - WMJ : official publication of the State Medical Society of Wisconsin
PY  - 2026
AN  - PMID:42623630
ER  - 

摘要

INTRODUCTION: Severe hypercholesterolemia in children is commonly caused by familial hypercholesterolemia (FH); however, sitosterolemia, a rare autosomal recessive disorder, should be considered when FH genetic testing is negative. CASE PRESENTATION: A 4-year-old boy presented with xanthomas on his knees. His total cholesterol was 561 mg/dL. Initially, homozygous FH was suspected, and rosuvastatin was started; however, genetic testing was negative. Subsequent genetic testing identified a homozygous ABCG8 variant, consistent with sitosterolemia. Rosuvastatin was discontinued, and ezetimibe and dietary plant sterol restriction were initiated, resulting in significant improvement in cholesterol levels and resolution of xanthomas. DISCUSSION: Sitosterolemia results from impaired ABCG5/8 transporter function, leading to plant sterol accumulation, which can cause hypercholesterolemia, xanthomas, and hematologic abnormalities. Diagnosis is established by demonstrating elevated plant sterol levels or through genetic testing. Treatment involves dietary plant sterol restriction and ezetimibe. CONCLUSIONS: Sitosterolemia, though rare, should be considered in severe hypercholesterolemia when FH genetic testing is negative. This case demonstrates a typical presentation and favorable response to treatment with ezetimibe and dietary modification.

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