[Pathohistologic diagnosis of cholesterol ester storage disease].
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Key Findings
Abstract
Cholesteryl ester storage disease (CESD) is rare and characterised by accumulation of cholesteryl esters and triglycerides in many tissues due to the deficiency of lysosomal acid lipase. We report on a 2 1/2-year old child with CESD. The diagnosis was made by liver biopsy and finding of heat-sensitive birefrigent crystals seen in frozen liver tissue under polarized light. In world literature the number of cases previously described is small (in paediatric age group does not exceed 40), and this was the reason for the presentation of our patient.
Affiliation
Department of Pathology, Dr. Vukan Chupitsh Mother and Child Health Institute, Belgrade.
External References
- PubMed ID:
- 11797452
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