Sato Atsuo, Umezawa Remi, Kurosawa Rumiko, Kajigaya Yasuhiko
Department of Pediatrics, Yokohama Sakae Kyosai Hospital.
Kansenshogaku Zasshi. 2002 Nov;76(11):963-6. doi: 10.11150/kansenshogakuzasshi1970.76.963.
A case of human parvovirus B19 (B19) infection is reported. A 6-year-old previously healthy girl was admitted to our hospital complaining of slight fever and petechial hemorrhage on her neck, trunk and the proximal parts of extremities. On admission, the platelet count was within normal range (180 x 10(3)/microliter) but white blood cells and reticulocytes were moderately suppressed (2.4 x 10(3)/microliter and 1@1000, respectively). The purpura disappeared in a week and the blood cell counts fully recovered without any specific treatment. Detection of B19 DNA and anti-B19 IgM antibody in the serum on admission led to the final diagnosis. Since the cellular receptor for B19, the blood group P antigen, is expressed on vascular endothelial cells as well as erythroid progenitor cells, the purpura was considered to be the result of direct vascular injury. She was very unique as she subsequently exhibited papular-purpuric gloves and socks syndrome and erythema infectiosum during follow-up. This case may provide a new insight into the pathogenesis of cutaneous manifestations of B19 infection.
报告了一例人类细小病毒B19(B19)感染病例。一名6岁既往健康的女孩因发热以及颈部、躯干和四肢近端出现瘀点性出血而入院。入院时,血小板计数在正常范围内(180×10³/微升),但白细胞和网织红细胞受到中度抑制(分别为2.4×10³/微升和1/1000)。未经任何特殊治疗,紫癜在一周内消失,血细胞计数完全恢复。入院时血清中B19 DNA和抗B19 IgM抗体的检测得出了最终诊断。由于B19的细胞受体血型P抗原在血管内皮细胞和红系祖细胞上均有表达,紫癜被认为是直接血管损伤的结果。她非常独特,因为在随访期间随后出现了丘疹紫癜性手套和袜套综合征以及传染性红斑。该病例可能为B19感染皮肤表现的发病机制提供新的见解。