利妥昔单抗成功治疗ABO错配HSCT后的纯红细胞发育不全和慢性GVH

S. Haidouri, Mehtat Em, S. Jennane, H. Elmaaroufi, M. Mikdame, K. Doghmi
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引用次数: 0

摘要

背景:纯红细胞发育不全(PRCA)是ABO血型错配造血干细胞移植的罕见并发症;没有标准的护理,在这里我们报告一例成功的利妥昔单抗治疗难治性PRCA和慢性移植物抗宿主病。病例介绍:一名26岁的女性,慢性髓性白血病伴类固醇难治性慢性肝移植物抗宿主病,在接受异基因HSCT治疗后出现PRCA,每周使用4剂量的利妥昔单抗375mg/m²,其血红蛋白水平升高,肝脏酶改善。结论:本病例的兴趣是报告利妥昔单抗的重要治疗效果,在文献中广泛使用,特别是慢性移植物抗宿主病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Treatment of Pure Red Cell Aplasia and Chronic GVH with Rituximab after ABO Mismatched HSCT
Background: Pure Red Cell Aplasia (PRCA) is a rare complication of ABO mismatched hematopoietic stem cell transplantation; there isn’t no standard of care, here we report a case of successful treatment by Rituximab in a refractory PRCA and chronic graft versus host disease. Case Presentation: A 26-year-old woman with PRCA following ABOmismatched allogeneic HSCT for chronic myeloid leukemia, associated with steroid refractory chronic hepatic graft versus host disease, treated with 4 doses of Rituximab 375mg/m² weekly, with an increase in her hemoglobin level and improvement of her liver’s enzymes. Conclusion: The interest of this case is to report the important therapeutic result of Rituximab, widely used in literature, especially if chronic Graft Versus host disease is associated.
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