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[遗传性球形红细胞增多症中的再生障碍危象]

[Aplastic crises in hereditary spherocytosis].

作者信息

Pekrun A, Eiffert H, Eber S W, Schröter W

机构信息

Universitäts-Kinderklinik und Poliklinik, Universität Göttingen.

出版信息

Monatsschr Kinderheilkd. 1988 Apr;136(4):173-5.

PMID:2838746
Abstract

Parvovirus B19-infections are diagnosed with increasing frequency. In addition to erythema infectiosum they cause a temporary red cell aplasia of 5-10 days duration, in patients with hemolytic anemia an aplastic crisis as demonstrated in 5 patients with hereditary spherocytosis. In every case an acute infection by parvovirus B19 could be diagnosed. Hemoglobin concentrations dropped to 4.0-6.2 g/dl, reticulocytes were diminished to 0-25,000/microliters. In every case there followed a complete recovery of erythropoiesis after 2-3 days.

摘要

细小病毒B19感染的诊断频率日益增加。除传染性红斑外,它还会导致持续5至10天的暂时性红细胞再生障碍,在溶血性贫血患者中会引发再生障碍危象,如在5例遗传性球形红细胞增多症患者中所证实的那样。在每一例中,均可诊断出细小病毒B19的急性感染。血红蛋白浓度降至4.0 - 6.2 g/dl,网织红细胞减少至0 - 25,000/微升。在每一例中,2至3天后红细胞生成均完全恢复。

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