Wiersbitzky S, Schwarz T F, Ladstätter L, Bruns R, Abel E, Deinhardt F, Roggendorf M, Paul W, Jäger G, Hottenträger B
Klinik für Kindermedizin, Ernst-Moritz-Arndt-Universität Greifswald.
Kinderarztl Prax. 1991 Oct;59(10):302-6.
The human parvovirus B19 provokes erythema infectiosum ("e.i."); moreover there is a wide range of diseases due to parvovirus B19 without exanthema/rash. The erythropoietic blast cells of the bone marrow seems to be the main target cells for this virus. Therefore in cases of prenatal infection the consequences are extremely similar to fetal erythroblastosis ("non-immunological" fetal hydrops). In postnatal life the parvovirus B19 infection causes hyporegenerative phases of the erythropoiesis with anaemia after 3-4 weeks. We studied the white blood cell count (WBC), erythrocytes and thrombocytes in children suffering from (serologically well documented) parvovirus B19 infection with exanthem/"e.i." (group 1; n = 23), without exanthem (group 2; n = 46) and with unknown febrile exanthematous rashes (group 3; n = 76). We did not find any characteristic data in the WBC for a diagnosis of parvovirus B19 infection. However we have for the first time documented a significant thrombocytopenia in "e.i." (group 1) not found in group 2. The thrombocytopenia appears earlier than the anaemia, because the lifespan of thrombocytes is considerably shorter than that of erythrocytes. These data suggest that parvovirus B19 attacks not only "erythropoietic" blast cells but also immature bone marrow cells, which are later responsible for the thrombocytopoiesis.
人细小病毒B19可引发传染性红斑(“e.i.”);此外,由细小病毒B19引起的无皮疹/疹的疾病种类繁多。骨髓中的成红细胞似乎是该病毒的主要靶细胞。因此,在产前感染的情况下,后果与胎儿成红细胞增多症(“非免疫性”胎儿水肿)极为相似。在出生后的生活中,细小病毒B19感染会导致红细胞生成的再生低下期,并在3 - 4周后出现贫血。我们研究了患有(血清学充分记录)伴有皮疹的细小病毒B19感染的儿童(“e.i.”)(第1组;n = 23)、无皮疹的儿童(第2组;n = 46)以及伴有不明发热性皮疹的儿童(第3组;n = 76)的白细胞计数(WBC)、红细胞和血小板。我们未在白细胞中发现任何用于诊断细小病毒B19感染的特征性数据。然而,我们首次记录到第1组(“e.i.”)中存在显著的血小板减少症,而第2组未发现。血小板减少症比贫血出现得更早,因为血小板的寿命比红细胞短得多。这些数据表明,细小病毒B19不仅攻击“红细胞生成性”成红细胞,还攻击未成熟的骨髓细胞,这些细胞随后负责血小板生成。