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Pathology of hepatic iron overload Deugnier Y; Turlin BWorld J Gastroenterol 2007[Sep]; 13 (35): 4755-60Although progress in imaging and genetics allow for a noninvasive diagnosis of most cases of genetic iron overload, liver pathology remains often useful (1) to assess prognosis by grading fibrosis and seeking for associated lesions and (2) to guide the etiological diagnosis, especially when no molecular marker is available. Then, the type of liver siderosis (parenchymal, mesenchymal or mixed) and its distribution throughout the lobule and the liver are useful means for suggesting its etiology: HLA-linked hemochromatosis gene (HFE) hemochromatosis or other rare genetic hemochromatosis, nonhemochromatotic genetic iron overload (ferroportin disease, aceruloplasminemia), or iron overload secondary to excessive iron supply, inflammatory syndrome, noncirrhotic chronic liver diseases including dysmetabolic iron overload syndrome, cirrhosis, and blood disorders.|Hemochromatosis Protein[MESH]|Histocompatibility Antigens Class I/genetics[MESH]|Humans[MESH]|Iron Overload/diagnosis/*etiology/*pathology[MESH]|Liver Cirrhosis/metabolism/pathology[MESH]|Liver Diseases/complications[MESH]|Liver/metabolism/*pathology[MESH]|Membrane Proteins/genetics[MESH]|Mutation/genetics[MESH] |
