Khelif A, Vu Van H, Tremisi J P, Alfonsi F, Perrot D, Motin J, Viala J J
Scand J Haematol. 1985 Jan;34(1):13-5. doi: 10.1111/j.1600-0609.1985.tb00737.x.
A 22-year-old woman had an idiopathic pure red cell aplasia that failed to respond to high doses of corticosteroids. After a series of 10 plasma exchange procedures, bone marrow erythropoiesis and reticulocyte blood count returned to normal; the haematological remission has been now persistent for 12 months. The place of plasma exchange in the management of pure red cell aplasia and its mode of action will be discussed.
一名22岁女性患有特发性纯红细胞再生障碍性贫血，对高剂量皮质类固醇治疗无效。在进行了10次血浆置换后，骨髓红细胞生成和网织红细胞计数恢复正常；血液学缓解目前已持续12个月。本文将讨论血浆置换在纯红细胞再生障碍性贫血治疗中的地位及其作用机制。
