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纯合子镰状细胞病中的细小病毒相关再生障碍性危象

Parvovirus associated aplastic crisis in homozygous sickle cell disease.

作者信息

Goldstein A R, Anderson M J, Serjeant G R

出版信息

Arch Dis Child. 1987 Jun;62(6):585-8. doi: 10.1136/adc.62.6.585.

Abstract

Aplastic crises in homozygous sickle cell disease in Jamaica predominantly affect children and occur in epidemics. Of 67 cases in a cohort study of 314 children with homozygous sickle cell disease, 62 were attributable to human parvovirus infection. Affected children were aged 0.5-12.5 years, and the incidence rose to 28% by 10 years. No recurrences were seen. Symptoms and signs on presentation were attributable to the viraemia and acute anaemia. Asymptomatic thrombocytopenia was common. Blood transfusion was given in 54 cases (87%). Thirty eight children (61%) were admitted to hospital, 16 of whom were extremely ill on presentation and one of whom died soon after admission. Twenty four (39%) were managed as outpatients, 16 of whom were transfused. Parvovirus associated aplastic crisis is a self limited condition with excellent prognosis if diagnosed promptly and managed appropriately.

摘要

牙买加纯合子镰状细胞病的再生障碍性危象主要影响儿童,且呈流行性发生。在一项对314名纯合子镰状细胞病儿童的队列研究中的67例病例中,62例归因于人类细小病毒感染。受影响儿童年龄在0.5至12.5岁之间,到10岁时发病率升至28%。未见复发情况。就诊时的症状和体征归因于病毒血症和急性贫血。无症状性血小板减少很常见。54例(87%)接受了输血。38名儿童(61%)住院,其中16名就诊时病情极重,1名入院后不久死亡。24名(39%)作为门诊患者处理,其中16名接受了输血。细小病毒相关的再生障碍性危象是一种自限性疾病,如果及时诊断并适当处理,预后良好。

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本文引用的文献

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Salmonella septicemia and aplastic crisis in a patient with sickle-cell anemia.
Acta Paediatr (Stockh). 1961 Sep;50:517-21. doi: 10.1111/j.1651-2227.1961.tb08208.x.
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The aplastic crisis in sickle-cell anaemia.
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