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Iron Deficiency Anemia in Adult Onset Still's Disease with a Serum Ferritin of 26,387 μg/L

机译:血清铁蛋白为26,387μg/ L的成人发病静止病中的铁缺乏性贫血

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Serum ferritin rises in the anemia of chronic inflammation reflecting increased iron storage and other changes mediated by inflammation. When iron deficiency coexists, the ferritin may not always decline into the subnormal range. We describe the rare interaction of iron deficiency with the extreme hyperferritinemia characteristic of adult onset Still's disease. The combination has clinical relevance and allows deductions about the presence of serum ferritin at 26,387 μg/L despite obvious iron depletion. The diagnosis of iron deficiency anemia was delayed and became fully obvious when her Still's disease remitted and serum ferritin decreased to 6.5 μg/L. The coexistence of iron deficiency should be considered when evaluating a patient with anemia of chronic inflammation even when the ferritin level is elevated several hundredfold. Further insights on ferritin metabolism in Still's disease are suggested by the likelihood that the patient's massive hyperferritinemia in the acute phase of Still's disease was almost entirely of the iron-free apoferritin form.
机译:血清铁蛋白在慢性炎症性贫血中升高,反映出铁存储增加以及炎症介导的其他变化。当铁缺乏症并存时,铁蛋白可能不会总是下降到亚正常范围内。我们描述了铁缺乏症与成年斯蒂尔氏病成年的极端高铁蛋白血症的罕见相互作用。该组合具有临床意义,尽管铁明显耗竭,但仍可推断血清铁蛋白含量为26,387μg/ L。当斯蒂尔氏病缓解且血清铁蛋白降至6.5μg/ L时,铁缺乏性贫血的诊断被延迟并变得完全明显。在评估慢性炎症性贫血患者时,应考虑铁缺乏症的共存,即使铁蛋白水平升高了数百倍也是如此。在斯蒂尔氏病急性期患者的大量高铁蛋白血症可能几乎完全是无铁的载铁蛋白形式,这提示了斯蒂尔氏病中铁蛋白代谢的进一步见解。

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