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Cytopenia and Bone Marrow Dysplasia in a Case of Wilson’s Disease

机译:威尔逊氏病引起的细胞减少症和骨髓发育不良

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摘要

We describe a sixteen year old with Wilson’s disease on copper chelation and subsequent high dose oral zinc who developed severe anemia and neutropenia. Bone marrow aspirate done to evaluate the cause of bicytopenia revealed trilineage dysplasia. Correlating the clinical context with bone marrow and biochemical parameters, copper deficiency was suspected and he was given a trial of therapy, following which the hematological parameters improved. This case highlights hypocupremia as a reversible cause of bone marrow dysplasia in patients with Wilson’s disease on chelation, where serum copper levels are not useful in the diagnosis. We also believe that monitoring of the blood counts in patients on copper chelation may provide a clue to impending copper deficiency.
机译:我们描述了一名16岁的患有铜螯合和随后的高剂量口服锌的威尔逊氏病,后者患有严重的贫血和中性粒细胞减少症。进行骨髓抽吸术以评估双血细胞减少症的原因显示三系发育异常。将临床情况与骨髓和生化参数相关联,怀疑铜缺乏,并对其进行了治疗试验,随后血液学参数得到改善。该病例突出显示,低螯合血症是威尔逊氏病螯合患者中骨髓异常增生的可逆原因,血清铜水平在诊断中无用。我们还认为,监测铜螯合患者的血球计数可能为即将出现的铜缺乏症提供线索。

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