Gerrits G P, van Oostrom C G, de Vaan G A, Bakkeren J A
Eur J Pediatr. 1984 Sep;142(4):266-70. doi: 10.1007/BF00540249.
In the period 1975-1983 22 patients, aged 4-36 months were seen with severe transient normochromic, normocytic anaemia caused by a transient erythroblastopenia. In 20 patients bone marrow aspirations were obtained; they showed erythroblastopenia. In ten cases we observed young lymphoid cells, suggesting a diagnosis of acute lymphoblastic leukaemia. One patient suspected of a leukaemia, was studied in more detail. All patients showed reticulocytopenia. MCV and HbF were within normal range. During recovery reticulocytosis and higher levels of HbF were found. Except for blood transfusion in most patients, therapy (e.g. corticosteroids) was not necessary. Spontaneous recovery is a feature of this kind of erythroblastopenia, contrasting with congenital hypoplastic anaemia.
在1975年至1983年期间,我们诊治了22例年龄在4至36个月的患儿,他们因短暂性成红细胞减少症而患有严重的短暂性正色素性、正细胞性贫血。20例患儿进行了骨髓穿刺;结果显示成红细胞减少。在10例患儿中,我们观察到幼稚淋巴细胞,提示急性淋巴细胞白血病的诊断。对1例疑似白血病的患儿进行了更详细的研究。所有患儿均表现为网织红细胞减少。平均红细胞体积(MCV)和胎儿血红蛋白(HbF)均在正常范围内。在恢复过程中,发现网织红细胞增多和HbF水平升高。除大多数患儿接受输血外,无需进行治疗(如使用皮质类固醇)。自发恢复是这种成红细胞减少症的一个特点,这与先天性再生障碍性贫血不同。