Seip M, Zanussi G F
Department of Paediatrics, National Hospital, Rikshospitalet, Oslo, Norway.
Acta Paediatr Scand. 1988 May;77(3):464-6. doi: 10.1111/j.1651-2227.1988.tb10682.x.
Two siblings with Diamond-Blackfan anaemia (DBA) and several congenital malformations were first treated with corticosteroids and blood transfusions. High steroid doses were needed, but in spite of this haemoglobin values periodically fell below acceptable levels. Cyclosporine was then given in addition to prednisolone. A slow increase in haemoglobin levels was observed over 2-3 months, and the prednisolone doses could be reduced gradually. Two short communications in the literature report similar experiences. Cyclosporine could be tried in DBA when reasonable corticosteroid doses do not give a satisfactory response. Since the main effect of cyclosporine is a specific inhibition of T-lymphocytes, the observed therapeutic effect in DBA indicates that T-lymphocytes may play an important role in the pathogenesis of this disease.
两名患有先天性纯红细胞再生障碍性贫血(DBA)并伴有多种先天性畸形的兄弟姐妹最初接受了皮质类固醇和输血治疗。需要高剂量的类固醇,但尽管如此,血红蛋白值仍会定期降至可接受水平以下。随后在泼尼松龙的基础上加用了环孢素。在2至3个月内观察到血红蛋白水平缓慢上升,泼尼松龙的剂量可以逐渐减少。文献中的两篇简短通讯报道了类似的经验。当合理剂量的皮质类固醇未产生满意疗效时,可尝试在DBA患者中使用环孢素。由于环孢素的主要作用是特异性抑制T淋巴细胞,因此在DBA中观察到的治疗效果表明T淋巴细胞可能在该疾病的发病机制中起重要作用。