A Case Report of Xanthoma in a Child: A Sign of Systemic Disease

Author:

Katakam Bhumesh Kumar12,Sunki Karthik3,Netha G Narsimha Rao3,Rani Sudha3

Affiliation:

1. Pediatric Dermatology Training Center, Gandhi Medical College and Hospital, Secunderabad, Telangana, India

2. Department of DVL, Government Medical College and Hospital, Suryapet, Telangana, India

3. Department of DVL, Gandhi Medical College and Hospital, Secunderabad, Telangana, India

Abstract

Xanthomas are localized lipid deposits within an organ system. They are often an important sign of systemic disease. An 11-year-old boy came with complaints of multiple asymptomatic raised lesions over elbows, hands, and knees for 1 year. Lipid profile showed increased levels (total serum cholesterol of 622.2 mg%). Biopsy was suggestive of tuberous xanthoma. His parent’s cholesterol levels were also elevated. Familial hypercholesterolemia (FH) is a common genetic disease in which high low-density lipoprotein cholesterol levels are seen from the birth, and patients are at high risk for cardiovascular disease, cerebrovascular accidents, metabolic syndrome, and premature coronary death. Early detection of FH and early treatment is imperative to reduce morbidity and mortality.

Publisher

Medknow

Subject

Psychiatry and Mental health,Neuropsychology and Physiological Psychology

Reference10 articles.

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3. Familial hypercholesterolemia-epidemiology, diagnosis, and screening;Singh;Curr Atheroscler Rep,2015

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5. A receptor-mediated pathway for cholesterol homeostasis;Brown;Science,1986

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