Nibu K, Matsumoto I, Yanai F, Nunoue T
Nihon Ketsueki Gakkai Zasshi. 1989 Nov;52(7):1117-21.
Human parvovirus B19 is known to cause aplastic crisis in patients with hemolytic anemias due to cytotoxic effect of the infection to erythroid progenitor cells. We report here the first case of aplastic crisis by B19 in a patient with glucose-6-phosphate dehydrogenase deficiency. A five-year-old boy was admitted to the hospital because of severe anemia, fever and jaundice. Four weeks after admission, he developed erythema infectiosum. B19 infection was confirmed using countercurrent immunoelectrophoresis, Southern blotting and hybridization method, and radioimmunoassay for B19 specific IgM. B19 virus antigen was detected by an indirect immunofluorescent method in both the cytoplasm and nucleus of large mononuclear cells that had no granules in bone marrow. On admission, the hemoglobin was 3.1 g/dl and no reticulocytes were detected in the peripheral blood smear. Bone marrow examination revealed a normocellular marrow with erythroid hypoplasia and M/E ratio of 7.38. Large basophilic erythroblasts containing vacuoles were also noticed. Elevation of indirect bilirubin and hemoglobinuria suggested intravascular hemolysis. Transient mild thrombocytopenia associated with increased PAIgG was observed. It is likely that B19 virus infection caused hemolysis which contributed to severe anemia.
已知人类细小病毒B19可因感染对红系祖细胞的细胞毒性作用,导致溶血性贫血患者发生再生障碍危象。我们在此报告首例葡萄糖-6-磷酸脱氢酶缺乏患者因B19病毒引发再生障碍危象的病例。一名5岁男孩因严重贫血、发热和黄疸入院。入院四周后,他患上传染性红斑。通过对流免疫电泳、Southern印迹杂交法以及B19特异性IgM放射免疫测定法确诊为B19感染。采用间接免疫荧光法在骨髓中无颗粒的大单核细胞的细胞质和细胞核中均检测到B19病毒抗原。入院时,血红蛋白为3.1 g/dl,外周血涂片未检测到网织红细胞。骨髓检查显示骨髓细胞正常,但红系发育不全,M/E比值为7.38。还发现了含有空泡的嗜碱性大幼红细胞。间接胆红素升高和血红蛋白尿提示血管内溶血。观察到短暂性轻度血小板减少伴PAIgG升高。很可能是B19病毒感染导致溶血,进而造成严重贫血。