Davis R B, Farver M L
Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68198-3330.
Acta Haematol. 1994;92(1):29-32. doi: 10.1159/000204133.
We report the case of a 21-year-old male who presented with severe anemia and hypercellular bone marrow, without known cause. The dominant feature of the bone marrow was that of a maturation arrest in the erythroid series, with absolute reticulocytopenia in the peripheral blood. Immunosuppressive therapy was withheld, but transfusions were given to maintain his hemoglobin prior to full recovery. The patient had features of both pure red cell anemia and of transient erythroblastopenia of childhood.
我们报告了一例21岁男性病例，该患者出现严重贫血和骨髓细胞增多，但病因不明。骨髓的主要特征是红系成熟停滞，外周血中绝对网织红细胞减少。未进行免疫抑制治疗，但在完全康复前给予输血以维持其血红蛋白水平。该患者具有纯红细胞贫血和儿童期短暂红细胞生成减少症的特征。
