Etzioni A, Atias D, Pollack S, Levy J, Vardi P, Hazani H, Benderly A
Am J Hematol. 1986 Aug;22(4):409-14. doi: 10.1002/ajh.2830220410.
A 10-year-old girl with multiple endocrinopathies, hypoparathyroidism, and pernicious anemia subsequently developed pure red cell aplasia, which responded only temporarily to cytotoxic therapy. Because of transfusion dependency, resistance to steroids, plasmapheresis, and Cytoxan, she was given injections of intramuscular gammaglobulin. The injections caused a prompt and sustained rise in the child's erythropoiesis.
一名患有多种内分泌病、甲状旁腺功能减退和恶性贫血的10岁女孩随后发展为纯红细胞再生障碍性贫血，细胞毒性疗法仅使其暂时缓解。由于依赖输血、对类固醇、血浆置换和环磷酰胺耐药，她接受了肌肉注射丙种球蛋白治疗。注射后患儿的红细胞生成迅速且持续增加。
