静脉切开术
转铁蛋白饱和度
医学
肝细胞癌
肝硬化
胃肠病学
肝活检
铁蛋白
血色病
内科学
纤维化
活检
血清铁蛋白
作者
Heinz Zoller,Benedikt Schaefer,Annick Vanclooster,Bill Griffiths,Édouard Bardou-Jacquet,Elena Corradini,Graça Porto,John D. Ryan,Markus Cornberg
标识
DOI:10.1016/j.jhep.2022.03.033
摘要
Haemochromatosis is characterised by elevated transferrin saturation (TSAT) and progressive iron loading that mainly affects the liver. Early diagnosis and treatment by phlebotomy can prevent cirrhosis, hepatocellular carcinoma, diabetes, arthropathy and other complications. In patients homozygous for p.Cys282Tyr in HFE, provisional iron overload based on serum iron parameters (TSAT >45% and ferritin >200 μg/L in females and TSAT >50% and ferritin >300 μg/L in males and postmenopausal women) is sufficient to diagnose haemochromatosis. In patients with high TSAT and elevated ferritin but other HFE genotypes, diagnosis requires the presence of hepatic iron overload on MRI or liver biopsy. The stage of liver fibrosis and other end-organ damage should be carefully assessed at diagnosis because they determine disease management. Patients with advanced fibrosis should be included in a screening programme for hepatocellular carcinoma. Treatment targets for phlebotomy are ferritin <50 μg/L during the induction phase and <100 μg/L during the maintenance phase.
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