2019年高铁素血症的诊断

K. Serraj, S. Hamaz, Habiba Alaloui, H. Bachir, E. Andrès
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引用次数: 4

摘要

与低铁素血症不同,低铁素血症几乎总是反映缺铁,而高铁素血症在缺乏明显临床背景的情况下往往难以解释。在医学实践中,大于1000 μg/l的重度高铁素血症是典型的情况。Moore等人在2013年发表了一项内科为期2年的研究结果,发现627例最常见的癌症病因患者存在严重的高铁素血症[1]。Vardi等人发现了类似的结果,无论潜在原因如何,严重高铁蛋白血症都具有不良预后价值[2]。Lee等人的另一项更早的研究发现,在前两项研究中,高钙素血症的发生率相似,且同一患者的病因关联频率较高[3]。高铁素血症的高频率,其广泛的病因谱和经常同时存在的几种病因反映了需要在全球视野的基础上优先考虑最明显和最严重的原因来解决高铁素血症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnosis of hyperferritinemia in 2019
Unlike hypoferritinemia, which almost constantly reflects iron deficiency, hyperferritinemia is often difficult to interpret in the absence of an obvious clinical context. In medical practice, major hyperferritinemia greater than 1000 μg/l is a classic situation. Moore et al. had published in 2013 the results of a 2-year study in a department of internal medicine that found a major hyperferritinemia in 627 patients with the most common causes of cancer [1]. Vardi et al. found similar results with a pejorative prognostic value of severe hyperferritinemia, regardless underlying cause [2]. Another much older study by Lee et al. found similar frequencies of hyperritinemia in the previous two studies with high frequency of etiological associations in the same patients [3]. The high frequency of hyperferritinemia, their wide etiological spectrum and the frequent concomitant presence of several etiologies reflect the need to address hyperferritinemia based on a global vision prioritizing the most obvious and serious causes.
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