Sumimoto S, Kasajima Y, Hamamoto T, Miyanomae T, Iwai Y, Mayumi M, Mikawa H
Department of Paediatrics, Sumitomo Hospital, Osaka, Japan.
Eur J Pediatr. 1990 Jul;149(10):691-4. doi: 10.1007/BF01959523.
A girl developed acute agranulocytosis (45/mm3), 37 days after the onset of infectious mononucleosis. The bone marrow showed myeloid hyperplasia with maturation arrest and erythroid hypoplasia. A normal amount of colony forming units of granulocytes and macrophages (CFU-GM) colonies with a relative high number of clusters was observed. Neither anti-neutrophil antibodies nor circulating inhibitors of colony growth were found in serum. Granulocyte and macrophage colony stimulating factor (GM-CSF) activity in the patient's serum rose at this time. The agranulocytosis lasted 5 days and her clinical state soon improved. These results suggested that agranulocytosis was presumably not due to serum factors, including auto-antibodies and/or suppressive substances, and that Epstein-Barr virus (EBV) had some direct or indirect effect on the marrow cells of the myeloid series.
一名女孩在传染性单核细胞增多症发病37天后出现急性粒细胞缺乏症(45/mm³)。骨髓显示髓系增生伴成熟停滞和红系发育不全。观察到粒细胞和巨噬细胞集落形成单位(CFU-GM)集落数量正常,但簇的数量相对较高。血清中未发现抗中性粒细胞抗体和循环性集落生长抑制剂。此时患者血清中的粒细胞和巨噬细胞集落刺激因子(GM-CSF)活性升高。粒细胞缺乏症持续了5天,她的临床状态很快得到改善。这些结果表明,粒细胞缺乏症可能不是由包括自身抗体和/或抑制物质在内的血清因素引起的,并且爱泼斯坦-巴尔病毒(EBV)对髓系骨髓细胞有一些直接或间接影响。