Berlin G, Liedén G
Scand J Haematol. 1986 Jan;36(1):121-2. doi: 10.1111/j.1600-0609.1986.tb02663.x.
A 57-year-old man with idiopathic pure red cell aplasia went into remission after plasma exchange. He relapsed after 5 months and then failed to respond to treatment with intensive plasma exchange and immunosuppressive agents. Because of a high proportion of T-suppressor cells in the peripheral blood he was treated with lymphocytapheresis in addition to the previous treatment. The patient achieved a long-term haematological remission which has now persisted for more than 3 yr.
一名57岁的特发性纯红细胞再生障碍性贫血男性患者在进行血浆置换后病情缓解。5个月后复发，随后对强化血浆置换和免疫抑制剂治疗无反应。由于外周血中抑制性T细胞比例较高，除了先前的治疗外，他还接受了淋巴细胞去除术治疗。该患者实现了长期血液学缓解，目前已持续超过3年。
