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[不明原因再生障碍危象中的隐匿性遗传性球形红细胞增多症]

[Occult hereditary spherocytosis in aplastic crisis of unknown cause].

作者信息

Hansen J B, Ibsen J S, Pedersen G, Jensen S

机构信息

Aalborg Sygehus, medicinsk haematologisk afdeling B.

出版信息

Ugeskr Laeger. 1993 Nov 29;155(48):3928-30.

PMID:8273201
Abstract

We describe two cases of aplastic crisis of unknown origin, occurring within one week in a 49-year old man and his 20 year old son. They both had undiagnosed hereditary spherocytosis, and both of them had earlier had a B19-parvo infection without having symptoms of aplastic crisis at the same time. Chronic haemolytic anaemia should be considered in adult patients with acute severe anaemia caused by aplastic crisis.

摘要

我们描述了两例不明原因再生障碍性危象的病例,一名49岁男子及其20岁儿子在一周内相继发病。他们均患有未确诊的遗传性球形红细胞增多症,且两人此前都曾感染过B19细小病毒,但未同时出现再生障碍性危象的症状。对于因再生障碍性危象导致急性重度贫血的成年患者,应考虑慢性溶血性贫血。

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