Hansen J B, Ibsen J S, Pedersen G, Jensen S
Aalborg Sygehus, medicinsk haematologisk afdeling B.
Ugeskr Laeger. 1993 Nov 29;155(48):3928-30.
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.
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。
