Dhumeaux D, Hezode C
Service d'Hépatologie et de Gastroentérologie, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris, Créteil.
Bull Acad Natl Med. 2000;184(2):349-54.
Iron accumulation in the liver is frequently observed in hepatic diseases whatever their etiologies. In the majority of cases, there is no true overload, and iron accumulation corresponds to deposits in macrophages secondary to iron release from damaged hepatocytes. More rarely, namely in severe cirrhosis, there is a true overload, which is probably related to iron intestinal hyperabsorption. In such case, the site of iron excess is hepatocytic. Except for hemochromatosis, mutations of HFE gene do not play a major role in iron overload. In chronic liver diseases, iron overload could favor the development of hepatocellular carcinoma, even in the absence of cirrhosis.
无论病因如何,肝脏疾病中经常观察到肝脏铁蓄积。在大多数情况下,不存在真正的铁过载,铁蓄积对应于受损肝细胞释放铁后巨噬细胞中的沉积。更罕见的情况,即在严重肝硬化中,存在真正的铁过载,这可能与肠道铁吸收过多有关。在这种情况下,铁过量的部位是肝细胞。除血色素沉着症外,HFE基因突变在铁过载中不起主要作用。在慢性肝病中,即使没有肝硬化,铁过载也可能促进肝细胞癌的发展。