Dan K, Ito T, Nomura T
Third Department of Internal Medicine, Nippon Medical School, Tokyo, Japan.
Am J Hematol. 1990 Feb;33(2):148-50. doi: 10.1002/ajh.2830330215.
A rare case of pure red cell aplasia (PRCA) in association with pernicious anemia is reported. A 40-year-old man presented with typical clinical and laboratory features of pernicious anemia and received intramuscular injections of vitamin B12, with satisfactory response. Anemia recurred 6 months later despite continued therapy, and the patient was noted to have PRCA, which was treated successfully with two courses of high-dose bolus methylprednisolone therapy. His peripheral mononuclear cells before the therapy suppressed colony formation of early erythroid precursors (BFU-E) from normal bone marrow; such a suppressive effect was not found after recovery from anemia.
报告了一例罕见的与恶性贫血相关的纯红细胞再生障碍性贫血(PRCA)病例。一名40岁男性表现出恶性贫血的典型临床和实验室特征,接受了维生素B12肌肉注射,反应良好。尽管持续治疗,但6个月后贫血复发,该患者被诊断为PRCA,通过两个疗程的大剂量冲击甲基强的松龙治疗成功治愈。治疗前他的外周血单个核细胞抑制了正常骨髓中早期红系前体细胞(BFU-E)的集落形成;贫血恢复后未发现这种抑制作用。