Cholesteryl ester storage disease. Report of a case.

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Data

1987-07-01

Autores

Coelho, C. A.
Balarin, M. A.
Coelho, Kunie Iabuki Rabello [UNESP]

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Resumo

Cholesteryl ester storage disease (CESD) is a rare disorder of familial incidence characterized by the accumulation of cholesteryl ester and triglycerides in the liver, intestine and bone marrow. Until now only 21 cases have been reported in the literature. We present a 9 months old girl presenting with increased abdominal girth. She had normal liver function tests and increased cholesterol and triglycerides serum levels. The liver biopsy showed many cholesterol cristals seen as needle shaped cristals under polarized light. This is the youngest patient being diagnosed clinically in the literature.

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Palavras-chave

cholesterol, triacylglycerol, blood, case report, cholesterol ester storage disease, female, hepatomegaly, human, infant, liver disease, review, Case Report, Cholesterol, Cholesterol Ester Storage Disease, Female, Hepatomegaly, Human, Infant, Liver Diseases, Triglycerides

Como citar

Arquivos de Gastroenterologia, v. 24, n. 3-4, p. 184-187, 1987.