Histopathological Findings in Cholesteryl Ester Storage Disease: A Report of Three Cases

AuthorIraj Shahramianen
AuthorEsmaeil Azimi-khatibien
AuthorFatemeh Mahjooben
AuthorAliyeh Sargazien
AuthorMojtaba Delaramnasaben
AuthorAli Bazien
OrcidIraj Shahramian [0000-0002-4134-1405]en
OrcidMojtaba Delaramnasab [0000-0002-2958-3671]en
OrcidAli Bazi [0000-0003-4872-1352]en
Issued Date2017-07-31en
AbstractCholesteryl ester storage disease (CESD) is a disorder in which cholesteryl esters (CE) and triglycerides (TG) are preserved particularly in hepatocytes. The exact clinical manifestation is not known due to a lack of sufficient data. The current study presents 3 new cases of CESD with 2 of them being siblings. All had perturbed serum low-density lipoprotein (LDL), lactate dehydrogenase (LDH), triglyceride, and cholesterol. Hepatosplenomegaly was seen in all the patients. Liver biopsy showed fat storage in hepatocytes. Adrenomegaly or adrenal calcification, portal hypertension, esophageal varices, and hepatic scarring were not observed in any of the patients. Histopathologic features of CESD, including fat storage in hepatocytes, could characterize these patients.en
DOIhttps://doi.org/10.5812/gct.58187en
KeywordCholesteryl Ester Storage Diseaseen
KeywordLysosomal Storage Diseasesen
KeywordLipidosesen
KeywordHepatologyen
KeywordHistopathologyen
KeywordTriglycerideen
PublisherBrieflandsen
TitleHistopathological Findings in Cholesteryl Ester Storage Disease: A Report of Three Casesen
TypeCase Reporten

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