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[一名患有自身免疫性溶血性贫血和B细胞非霍奇金淋巴瘤的患者因人类细小病毒B19感染导致严重贫血]

[Severe anaemia caused by Human Parvovirus B19 infection in a patient with autoimmune haemolytic anaemia and a B-cell non-Hodgkin lymphoma].

作者信息

van Dam I E, Kater A P, Hart W, van den Born B J H

机构信息

Academisch Medisch Centrum/Universiteit van Amsterdam, Meibergdreef, Amsterdam.

出版信息

Ned Tijdschr Geneeskd. 2008 Jan 19;152(3):153-7.

Abstract

A 65-year-old man with a 15-year history of 'leukemicised' low-grade lymphocytic B-cell non-Hodgkin lymphoma with a low-titre of IgM kappa paraprotein was admitted with severe anaemia and reticulocytopenia. Treatment with prednisone and chlorambucil had been started two weeks earlier because of a recently diagnosed Coombs-positive haemolytic anaemia. He also received a blood transfusion at that time. During his stay in the hospital, a crista biopsy was performed that revealed no signs of bone marrow suppression but markedly enlarged pro-erythroblasts. Although a serologic test for Human Parvovirus-B19 was negative, PCR showed a sharply increased viral load with more than 1 x 10(11) copies/ml, compatible with a primary parvovirus infection. In retrospect, an earlier transfusion of blood that had not been screened for parvovirus was probably the culprit. Treatment with human immunoglobulin was effective in lowering the viral load and normalising the haemoglobin. This case illustrates that reticulocytopenia in a patient with a haematologic disorder accompanied by a shortened erythrocyte life-span is suggestive for a primary parvovirus infection, especially following a recent transfusion. To prevent transmission of Human Parvovirus B19 via blood transfusion, the Health Council of the Netherlands published a guideline indicating that patients at high risk for a complicated infection with Human Parvovirus B19 should be given 'virus-free' blood products.

摘要

一名65岁男性,有15年“白血病化”的低度B淋巴细胞性非霍奇金淋巴瘤病史,伴有低滴度IgM κ副蛋白,因严重贫血和网织红细胞减少入院。由于最近诊断为抗人球蛋白试验阳性的溶血性贫血,两周前开始使用泼尼松和苯丁酸氮芥治疗。当时他还接受了输血。住院期间,进行了嵴活检,结果显示无骨髓抑制迹象,但早幼红细胞明显增大。尽管人细小病毒B19的血清学检测为阴性,但聚合酶链反应显示病毒载量急剧增加,超过1×10(11)拷贝/毫升,符合原发性细小病毒感染。回顾既往,早期输注未筛查细小病毒的血液可能是病因。用人免疫球蛋白治疗可有效降低病毒载量并使血红蛋白恢复正常。该病例表明,血液系统疾病患者出现网织红细胞减少且红细胞寿命缩短提示原发性细小病毒感染,尤其是近期输血后。为防止人细小病毒B19通过输血传播,荷兰卫生委员会发布了一项指南,指出有发生复杂人细小病毒B19感染高风险的患者应输注“无病毒”血液制品。

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