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血色素沉着症的诊断。

Diagnosis of hemochromatosis.

作者信息

Powell Lawrie W

机构信息

Queensland Institute of Medical Research and The University of Queensland, Brisbane, Australia.

出版信息

Semin Gastrointest Dis. 2002 Apr;13(2):80-8.

Abstract

Hereditary hemochromatosis is an inherited disorder of iron metabolism affecting approximately 1 in 200 to 300 individuals of Northern European descent. Over time, the continued deposition of iron in parenchymal cells of many organs can eventually lead to diabetes mellitus, cardiomyopathy, and hepatic cirrhosis, the last of which is frequently followed by hepatocellular carcinoma. Although the complications of hereditary hemochromatosis can be devastating, its clinical management is simple and effective if the disease is identified early in its progression. In affected individuals, it is important to confirm or exclude the presence of cirrhosis and begin therapy as early as possible. The insidious onset and high prevalence of nonspecific symptoms in the early stages of the disease requires the clinician to have a high index of clinical suspicion for this disease. This is particularly important because treatment before there is permanent organ damage can reverse the iron toxicity and restore life expectancy to normal. Because of its familial occurrence all first-degree relatives of patients with hereditary hemochromatosis should be tested for the disease.

摘要

遗传性血色素沉着症是一种铁代谢的遗传性疾病,影响着约二十分之一至三百分之一的北欧血统个体。随着时间的推移,铁在许多器官实质细胞中的持续沉积最终可导致糖尿病、心肌病和肝硬化,其中肝硬化常继之以肝细胞癌。尽管遗传性血色素沉着症的并发症可能具有毁灭性,但如果在疾病进展早期就得以确诊,其临床管理简单且有效。对于受影响的个体,确认或排除肝硬化的存在并尽早开始治疗很重要。该病早期隐匿起病且非特异性症状患病率高,这就要求临床医生对该病有高度的临床怀疑指数。这一点尤为重要,因为在出现永久性器官损伤之前进行治疗可逆转铁毒性并使预期寿命恢复正常。由于其家族性发病,遗传性血色素沉着症患者的所有一级亲属都应接受该病检测。

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