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儿童早期因短暂性纯红细胞再生障碍导致的严重贫血。是在定向干细胞水平发生停滞吗?

Severe anemia due to transient pure red cell aplasia in early childhood. Arrest at the level of the committed stem cells?

作者信息

Tillmann W, Prindull G, Schröter W

出版信息

Eur J Pediatr. 1976 Aug 16;123(1):51-8. doi: 10.1007/BF00497680.

Abstract

Five patients, 11 months to 3 4/12 years old with severe normochromic, normocytis anemia and reticulocytopenia are reported. At the height of erythropoietic arrest when erythroid precursor cells were completely absent, undifferentiated stem cells (transitional cells), accumulated in the bone marrow. They disappeared again upon spontaneous resumption of erythropoiesis. We suggest that the erythropoietic arrest had occurred at the level of the hematopoietic stem cell. All patients recovered within 1 week of diagnosis. No steroid therapy was given. Failure to recognize this clinical entity leads to unnecessary diagnostic and therapeutic procedures including the transfusion of blood.

摘要

报告了5例年龄在11个月至3又4/12岁的患者,他们患有严重的正色素性、正细胞性贫血和网织红细胞减少症。在红细胞生成停滞的高峰期,当红系前体细胞完全缺失时,未分化的干细胞(过渡细胞)在骨髓中积聚。当红细胞生成自发恢复时,它们又消失了。我们认为红细胞生成停滞发生在造血干细胞水平。所有患者在诊断后1周内康复。未给予类固醇治疗。未能识别这种临床实体会导致不必要的诊断和治疗程序,包括输血。

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