特发性血色病(Idiapathin hemochromatosis)又称色素性肝硬化(Pigmentory cirrhosis),古铜色糖尿病(Bronze diabetes),细胞色素沉着症(Cytosiderosis),是一种遗传性代谢异常、铁在体内缓慢积聚的罕见疾病,我院最近收治一例。患者男,52岁,主因肝大22年,多饮、多食、多尿5个月,于1986年8月4日入院。患者于1964年体检时发现肝大,但肝功能正常,亦无自觉症状。嗣后多次查体发现肝脏逐渐增大,仍无肝区疼痛、无厌 Idiopathic hemochromatosis, also known as Pigmentory cirrhosis, Bronze diabetes, Cytosiderosis, is an uncommon genetic abnormality in which iron slowly accumulates in the body Disease, our hospital recently admitted to a case. Male patient, 52 years old, the main liver for 22 years, drink more, eat more, polyuria for 5 months, on August 4, 1986 admission. Patients in 1964 when the liver was found, but normal liver function, there are no symptoms. Subsequent examination found that the liver gradually increased, still no pain in the liver area, insensitive