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Pure red cell aplasia due to parvovirus B19 infection after liver transplantation: A case report and review of the literature

机译:肝移植术后细小病毒B19感染引起的纯红细胞发育不全:一例病例报告并文献复习

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摘要

Pure red cell aplasia (PRCA) due to parvovirus B19 (PVB19) infection after solid organ transplantation has been rarely reported and most of the cases were renal transplant recipients. Few have been described after liver transplantation. Moreover, little information on the management of this easily recurring disease is available at present. We describe the first case of a Chinese liver transplant recipient with PVB19-induced PRCA during immunosuppressive therapy. The patient suffered from progressive anemia with the lowest hemoglobin level of 21 g/L. Bone marrow biopsy showed selectively inhibited erythropoiesis with giant pronormoblasts. Detection of PVB19-DNA in serum with quantitative polymerase chain reaction (PCR) revealed a high level of viral load. After 2 courses of intravenous immunoglobulin (IVIG) therapy, bone marrow erythropoiesis recovered with his hemoglobin level increased to 123 g/L. He had a low-level PVB19 load for a 5-mo follow-up period without recurrence of PRCA, and finally the virus was cleared. Our case indicates that clearance of PVB19 by IVIG in transplant recipients might be delayed after recovery of anemia.
机译:实体器官移植后因细小病毒B19(PVB19)感染而引起的纯红细胞发育不良(PRCA)很少见,大多数病例为肾移植受者。肝移植后几乎没有记载。而且,目前关于这种易复发疾病的治疗的信息很少。我们描述了第一例中国肝移植受者在免疫抑制治疗期间PVB19诱导的PRCA。该患者患有进行性贫血,最低血红蛋白水平为21 g / L。骨髓活检显示巨生原核细胞选择性抑制红细胞生成。用定量聚合酶链反应(PCR)检测血清中的PVB19-DNA显示高水平的病毒载量。经过2个疗程的静脉免疫球蛋白(IVIG)治疗后,骨髓红细胞生成得以恢复,他的血红蛋白水平增加到123 g / L。在为期5个月的随访期中,他的低水平PVB19负荷无PRCA复发,最终病毒被清除。我们的案例表明,在贫血恢复后,IVIG在移植受体中清除PVB19可能会延迟。

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