Gualdi C N
Minerva Med. 1977 Mar 31;68(16):1057-60.
After briefly recalling present-day clinical and experimental knowledge regarding chronic idiopathic erythroblastopenia, a case of chronic anaemia with definite aregenerative character is reported. The case was followed up for years; it was refractory to ordinary therapy, slightly and temporarily sensitive to immunosuppression, and nosographically classifiable as a transition form between primary global marrow aplasia and pure chronic erythroblastopenia not associated with thymoma.
在简要回顾了目前关于慢性特发性成红细胞减少症的临床和实验知识后,报告了一例具有明确再生障碍特征的慢性贫血病例。该病例进行了多年随访;对常规治疗无效,对免疫抑制有轻微且短暂的反应,在疾病分类学上可归类为原发性全骨髓再生障碍与不伴胸腺瘤的单纯慢性成红细胞减少症之间的过渡形式。