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Article in English | IMSEAR | ID: sea-39359

ABSTRACT

An 18-year-old woman had a hepatocellular adenoma of 4 cm across in the right lobe of the liver which was severely hemosiderotic because of beta-thalassemia hemoglobin E disease with numerous blood transfusions. The lesion was an accidental postmortem finding. To our knowledge, this is the second example of liver-cell adenoma occurring in a patient with beta-thalassemia hemoglobin E disease with secondary iron overload. It is suggested that this is an association between hepatocellular adenoma and secondary iron overload of liver cells, a similar event to the relation observed in hepatocellular carcinoma and secondary iron overload of hepatocytes.


Subject(s)
Adenoma, Liver Cell/etiology , Adolescent , Blood Transfusion/adverse effects , Female , Hemoglobin E/metabolism , Humans , Iron/metabolism , Liver Neoplasms/etiology , beta-Thalassemia/metabolism
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