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[特发性血色素沉着症——诊断与治疗]

[Idiopathic hemochromatosis--diagnosis and therapy].

作者信息

Schmidt U, Preu E, Tuschy U, Senf L, Herre K

出版信息

Z Gesamte Inn Med. 1984 Apr 15;39(8):152-60.

PMID:6730591
Abstract

The excessive storage of iron in idiopathic haemochromatosis leads to severe organic lesion up to life-threatening conditions (cardiac insufficiency, portal decompensation). The symptoms melanodermia , diabetes mellitus and other endocrine failures, liver cirrhosis, cardiac insufficiency and arthropathy appear together or in various combinations. The diagnosis is ascertained by the proof of iron storage, the multiple organic affection and by familial accumulation of the various laboratory diagnostic possibilities are particularly to be emphasized the serum iron value together with the percetal transferrin saturation (as search test), serum ferritin, the desferrioxamine test, simple ferrokinetic investigations and the quantitative determination of iron in the liver in the bioptate . For family examinations, apart from the search test, a HLA typisation is reasonable, in order to estimate the risk of the disease (particularly of brothers and sisters). The therapy of choice are blood- lettings (0.5 l once to twice a week) up to obtaining a permanent easy iron deficiency anaemia. The maintenance therapy should be performed with monthly to quarterly blood- lettings . Only in cases exception a desferal treatment is indicated. Endocrine failures and cardiac disturbances need a particular therapy.

摘要

特发性血色素沉着症中过量的铁储存会导致严重的器质性病变,甚至危及生命(心力衰竭、门脉失代偿)。症状包括皮肤黑色素沉着、糖尿病及其他内分泌功能衰竭、肝硬化、心力衰竭和关节病,这些症状可同时出现或有多种组合。诊断通过铁储存的证据、多种器官受累情况以及家族聚集性来确定。多种实验室诊断方法中,血清铁值及转铁蛋白饱和度(作为筛查试验)、血清铁蛋白、去铁胺试验、简单的铁动力学研究以及肝活检组织中铁的定量测定尤其值得重视。对于家族检查,除了筛查试验外,进行 HLA 分型是合理的,以便评估患病风险(尤其是兄弟姐妹)。首选治疗方法是放血(每周 1 至 2 次,每次 0.5 升),直至出现持续性轻度缺铁性贫血。维持治疗应每月至每季度进行一次放血。仅在极少数情况下才需要去铁胺治疗。内分泌功能衰竭和心脏疾病需要特殊治疗。

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