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两例肾移植受者因微小病毒 B19 感染致多发复发性纯红细胞再生障碍。

Two Cases of Kidney Transplant Recipients With Multiple Relapsing Pure Red Cell Aplasia Due to Parvovirus B19 Infection.

机构信息

From the Division of Hematology, Department of Internal Medicine, Bursa Uludag University, Bursa, Turkey.

出版信息

Exp Clin Transplant. 2024 Jan;22(1):75-79. doi: 10.6002/ect.2022.0145. Epub 2022 Oct 18.

Abstract

Although anemia is common after kidney transplant, pure erythroid aplasia due to parvovirus B19 infection is rare. Therefore, there are delays in diagnosis in transplant patients. Here, we aimed to raise awareness that pure red blood cell aplasia due to parvovirus B19 should be considered in the differential diagnosis of posttransplant anemia. Our report analyzes 2 kidney transplant recipients under immunosuppressive therapy who were diagnosed with pure red blood cell aplasia due to parvovirus B19 infection. Both patients were examined for anemia as a cause for transfusion dependence. Normochromic, normocytic anemia, and reticulocyte levels were low. Leukocyte and platelet counts and biochemical parameters were within reference ranges.Therefore, pure red blood cell aplasia associated with parvovirus B19 was included in the differential diagnosis. Bone marrow showed erythroid hypoplasia and megaloblastic changes with giant erythroblasts containing dark-stained inclusion structures. Results from the other series (neutrophils, lymphocytes, platelets) were within reference ranges. Parvovirus B19 immunoglobulin M and G levels were negative inbothpatients, yet serum parvovirus B19 DNA polymerase chain reaction test results were positive. Therefore, diagnosis was parvovirus B19-associated pure red blood cell aplasia. Anemia resolved completely by 4 weeks after reduction of immunosuppression and intravenous immunoglobulin. Both patients relapsed in month 5 of treatment. One patient relapsed 3 times during follow-up, with complete response to intravenous immunoglobulin for all 3 events.The second patient showed partial response to intravenous immunoglobulin after relapse. We suggest that pure red blood cell aplasia associated with parvovirus B19 should be considered in transplant patients who present with anemia and reticulocytopenia. Negative serology does not exclude thediagnosis, anditis important to perform a parvovirus B19 DNA polymerase chain reaction test. Intravenous immunoglobulin therapy is effective to cure anemia within weeks. Follow-up of patients is important because relapse may occur after treatment.

摘要

虽然肾移植后贫血很常见,但由于细小病毒 B19 感染引起的纯红细胞再生障碍性贫血较为罕见。因此,移植患者的诊断存在延迟。在这里,我们旨在提高认识,即细小病毒 B19 引起的纯红细胞再生障碍性贫血应在移植后贫血的鉴别诊断中考虑。我们的报告分析了 2 例接受免疫抑制治疗的肾移植受者,他们被诊断为细小病毒 B19 感染引起的纯红细胞再生障碍性贫血。两名患者均因贫血导致依赖输血而接受检查。正细胞正色素性贫血,网织红细胞水平较低。白细胞和血小板计数及生化参数均在参考范围内。因此,与细小病毒 B19 相关的纯红细胞再生障碍性贫血被纳入鉴别诊断。骨髓显示红系发育不良和巨幼细胞改变,含深染包涵体结构的巨红细胞。另一个系列(中性粒细胞、淋巴细胞、血小板)的结果在参考范围内。两名患者的细小病毒 B19 免疫球蛋白 M 和 G 水平均为阴性,但血清细小病毒 B19 DNA 聚合酶链反应检测结果均为阳性。因此,诊断为细小病毒 B19 相关的纯红细胞再生障碍性贫血。免疫抑制减少和静脉注射免疫球蛋白后 4 周内贫血完全缓解。两名患者在治疗的第 5 个月复发。一名患者在随访期间复发了 3 次,所有 3 次事件均对静脉注射免疫球蛋白完全有效。第二名患者在复发后对静脉注射免疫球蛋白有部分反应。我们建议,在出现贫血和网织红细胞减少的移植患者中,应考虑细小病毒 B19 相关的纯红细胞再生障碍性贫血。阴性血清学不能排除诊断,进行细小病毒 B19 DNA 聚合酶链反应检测很重要。静脉注射免疫球蛋白治疗可在数周内有效治愈贫血。对患者进行随访很重要,因为治疗后可能会复发。

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