Koi Satoshi, Arai Kosuke, Nogami Ayako, Toma Hayato, Yamamoto Masahide, Miura Osamu, Nagao Toshikage
Department of Hematology, Medical Hospital, Tokyo Medical and Dental University.
Clinical Laboratory Department, Medical Hospital, Tokyo Medical and Dental University.
Rinsho Ketsueki. 2020;61(10):1487-1491. doi: 10.11406/rinketsu.61.1487.
This is a case of a 75-year-old man who was on maintenance hemodialysis for 10 years due to diabetic nephropathy and was prescribed polaprezinc due to a low serum zinc level (55 µg/dl) and dysgeusia. Three months after the polaprezinc treatment was initiated, the patient developed pancytopenia, which persisted even after the serum zinc level was normalized and medication was discontinued. He was referred to our institute so that the progression of pancytopenia could be assessed. A blood biochemical examination revealed a WBC count of 1,700/µl, Hb level of 8.9 g/dl, and Plt count of 9.5×10/µl. A bone marrow aspirate smear showed slight megaloblastic changes and ringed sideroblasts in addition to an elevated WT1 mRNA level (76 copies/µg RNA) in the peripheral blood. Although these findings mimicked those of myelodysplasia, low serum copper (<2 µg/dl) and ceruloplasmin levels (3 mg/dl) were suggestive of hematopoietic abnormalities due to zinc-induced copper deficiency. Treatment with cocoa, a compound generally known to be rich in copper, gradually improved the pancytopenia and dysplastic bone marrow histology. This case indicates that clinicians should consider the risk of zinc-induced copper deficiency and its complications when zinc supplementation is administered to patients with chronic kidney disease, particularly those undergoing hemodialysis.
这是一例75岁男性患者,因糖尿病肾病接受维持性血液透析10年,因血清锌水平低(55μg/dl)和味觉障碍而服用泊拉普利锌。泊拉普利锌治疗开始三个月后,患者出现全血细胞减少,即使血清锌水平恢复正常且停药后仍持续存在。他被转诊至我院以评估全血细胞减少的进展情况。血液生化检查显示白细胞计数为1700/μl,血红蛋白水平为8.9g/dl,血小板计数为9.5×10/μl。骨髓穿刺涂片除显示外周血中WT1 mRNA水平升高(76拷贝/μg RNA)外,还显示有轻微巨幼样改变和环形铁粒幼细胞。尽管这些发现类似于骨髓增生异常,但低血清铜(<2μg/dl)和铜蓝蛋白水平(3mg/dl)提示锌诱导的铜缺乏导致造血异常。用通常已知富含铜的可可进行治疗逐渐改善了全血细胞减少和发育异常的骨髓组织学。该病例表明,临床医生在给慢性肾脏病患者,尤其是接受血液透析的患者补充锌时,应考虑锌诱导的铜缺乏及其并发症的风险。