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[人类细小病毒B19作为遗传性球形红细胞增多症再生障碍危象的病因]

[Human parvovirus B19 as the cause of aplastic crisis in hereditary spherocytosis].

作者信息

Fjaerli H O, Vogt H, Bruu A L

机构信息

Barneavdelingen Sentralsykehuset i Akershus, Nordbyhagen.

出版信息

Tidsskr Nor Laegeforen. 1991 Sep 20;111(22):2735-7.

PMID:1658972
Abstract

A seven months old boy was admitted to hospital for investigation and treatment of severe anaemia. The final diagnosis was hereditary spherocytosis. When, six weeks later, he developed an aplastic crisis, serological criteria provided evidence of recent human parvovirus B19 infection. The same disease was detected in the family. Human parvovirus B19 is shown to be of particular interest in aplastic crisis.

摘要

一名七个月大的男婴因严重贫血入院接受检查和治疗。最终诊断为遗传性球形红细胞增多症。六周后,他出现再生障碍性危象,血清学标准提供了近期感染人细小病毒B19的证据。在其家族中也检测到了同样的疾病。人细小病毒B19在再生障碍性危象中显示出特别的关联性。

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