Parvovirus B19 Infection as a Cause of Refractory Anemia in Kidney Transplant Recipients: A Case Series.

IF 0.8 Q4 UROLOGY & NEPHROLOGY
Indian Journal of Nephrology Pub Date : 2025-07-01 Epub Date: 2024-08-29 DOI:10.25259/IJN_127_2024
Umapati N Hegde, Ankur Mittal, Sishir Gang, Abhijit Konnur, Hardik Patel
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引用次数: 0

Abstract

Background: Kidney transplant recipients (KTRs) are at higher risk for infections, including parvovirus B19 (PVB19). This virus typically presents within the first-year posttransplant, causing anemia and potentially leading to increased morbidity and graft dysfunction.

Materials and methods: Charts of patients undergoing kidney transplantation between May 2013 and March 2022 were reviewed. Twenty-one patients had PVB19. Their clinical presentation, laboratory parameters, and outcomes were studied. The diagnosis of PVB19 was established by PVB19 DNA Polymerase Chain Reaction (PCR) and bone marrow examination (BME).

Results: Prevalence of PVB19 disease was 1.9% (21/1164) with a median onset time of 39 days posttransplantation. The most frequent clinical symptoms were fatigue reported by 76% of patients, followed by fever (47%), dyspnea (23%), and myalgia (33%). All patients (100%) developed anemia, while leukopenia and thrombocytopenia were observed in 14% and 9.5% of patients, respectively. Graft dysfunction was observed in 61.9% (13/21) patients. Diagnosis was confirmed by PCR in 20 out of 21 patients. One patient had a typical viral inclusion on BME. Immunosuppression, especially antiproliferative, was reduced in all patients. Eight patients received intravenous immunoglobulin, eight received packed cell blood transfusion, and seven received erythropoietin therapy. All patients recovered, with a median time of 30 days for hemoglobin levels to normalize. One patient had graft loss secondary to graft rejection.

Conclusion: PVB19, while uncommon, can be a significant cause of refractory anemia, particularly within the first-year posttransplant. Diagnosing PVB19 infection with PCR is crucial, and the primary treatment involves reducing immunosuppressants, especially antiproliferative agents.

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细小病毒B19感染是肾移植受者难治性贫血的原因:一个病例系列。
背景:肾移植受者(KTRs)感染的风险较高,包括细小病毒B19 (PVB19)。这种病毒通常在移植后一年内出现,引起贫血,并可能导致发病率增加和移植物功能障碍。材料与方法:回顾2013年5月至2022年3月肾移植患者的图表。21例患者有PVB19。研究了他们的临床表现、实验室参数和结果。通过PVB19 DNA聚合酶链反应(PCR)和骨髓检查(BME)确定PVB19的诊断。结果:PVB19疾病的患病率为1.9%(21/1164),中位发病时间为移植后39天。最常见的临床症状是76%的患者报告的疲劳,其次是发烧(47%)、呼吸困难(23%)和肌痛(33%)。所有患者(100%)均出现贫血,白细胞减少和血小板减少分别占14%和9.5%。61.9%(13/21)患者出现移植物功能障碍。21例患者中有20例经PCR确诊。一名患者在BME上有典型的病毒包涵体。所有患者的免疫抑制,尤其是抗增殖,均有所降低。8例患者接受静脉注射免疫球蛋白,8例接受填充细胞输血,7例接受促红细胞生成素治疗。所有患者均恢复,平均30天血红蛋白水平恢复正常。1例患者继发于移植物排斥。结论:PVB19虽然不常见,但可能是难治性贫血的重要原因,特别是在移植后一年内。用PCR诊断PVB19感染是至关重要的,主要治疗包括减少免疫抑制剂,特别是抗增殖药物。
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来源期刊
Indian Journal of Nephrology
Indian Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
1.40
自引率
0.00%
发文量
128
审稿时长
24 weeks
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