AI Article Synopsis

  • Hepatocellular adenomas (HCA) typically occur in middle-aged women using oral contraceptives, but can also affect men, children, and older women due to various conditions.
  • About 20% of HCA cases arise without oral contraceptive use, with obesity and inflammatory changes being common, while diagnosis can be complicated by background liver conditions such as fibrosis.
  • Identifying β-catenin mutations in HCA is crucial for assessing the risk of malignant transformation, and some nodules may already show signs of cancer, complicating the distinction between HCA and hepatocellular carcinoma.

Article Abstract

In Europe and North America, hepatocellular adenomas (HCA) occur, classically, in middle-aged woman taking oral contraceptives. Twenty percent of women, however, are not exposed to oral contraceptives; HCA can more rarely occur in men, children, and women over 65 years. HCA have been observed in many pathological conditions such as glycogenosis, familial adenomatous polyposis, MODY3, after male hormone administration, and in vascular diseases. Obesity is frequent particularly in inflammatory HCA. The background liver is often normal, but steatosis is a frequent finding particularly in inflammatory HCA. The diagnosis of HCA is more difficult when the background liver is fibrotic, notably in vascular diseases. HCA can be solitary, or multiple or in great number (adenomatosis). When nodules are multiple, they are usually of the same subtype. HNF1 α -inactivated HCA occur almost exclusively in woman. The most important point of the classification is the identification of β -catenin mutated HCA, a strong argument to identify patients at risk of malignant transformation. Some HCA already present criteria indicating malignant transformation. When the whole nodule is a hepatocellular carcinoma, it is extremely difficult to prove that it is the consequence of a former HCA. It is occasionally difficult to identify HCA remodeled by necrosis or hemorrhage.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652210PMC
http://dx.doi.org/10.1155/2013/253261DOI Listing

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