Zhu Kanger, Chen Jie, Chen Shengting
Department of Hematology, First Affiliated Hospital, Jinan University, Guangzhou, China.
Hematology. 2005 Oct;10(5):365-70. doi: 10.1080/10245330410001714202.
We report the first case of EBV-PTLD and pure red cell aplasia (PRCA) after an unrelated cord blood transplant in China, who was successfully treated with Rituximab.
Case report and literature review.
A 5-year-old girl with CML underwent a major ABO-incompatible HLA-identical unrelated cord blood transplantation (U-CBT) in January 2003. The post transplant course was complicated by PRCA. She presented on day +75 with fever, followed by rapid enlargement of tonsils, and a cluster of lymph nodes in the cervical and submandibular regions. A cervical lymph node biopsy revealed the histopathologic findings consistent with PTLD. The immunoblasts were shown to contain EBV viral genomic DNA by PCR, and immunocytochemistry study for the latent membrane protein 1 (LMP-1) and in situ hybridization for Epstein-Barr encoded RNAs1 (EBER1) were both positive. She responded rapidly to Rituximab and achieved complete resolution of clinical findings and symptoms of both EBV-PTLD and PRCA.
EBV-PTLD may occur with increasing frequency due to the increasing numbers of transplant recipients, transplant physician should be aware of this life-threatening complication. Rituximab alone may be an effective therapeutic strategy for patients who develop EBV-PTLD and PRCA after U-CBT.
我们报告中国首例非亲缘脐血移植后发生的EB病毒相关的移植后淋巴增殖性疾病(EBV-PTLD)和纯红细胞再生障碍性贫血(PRCA),该患者接受利妥昔单抗治疗后获得成功。
病例报告及文献复习。
一名5岁的慢性粒细胞白血病女童于2003年1月接受了主要ABO血型不合的HLA全相合非亲缘脐血移植(U-CBT)。移植后病程并发PRCA。她在+75天出现发热,随后扁桃体迅速肿大,颈部和颌下区有一群淋巴结。颈部淋巴结活检显示组织病理学结果符合PTLD。通过聚合酶链反应(PCR)显示免疫母细胞含有EBV病毒基因组DNA,针对潜伏膜蛋白1(LMP-1)的免疫细胞化学研究和针对爱泼斯坦-巴尔编码RNA1(EBER1)的原位杂交均为阳性。她对利妥昔单抗反应迅速,EBV-PTLD和PRCA的临床症状和体征完全消退。
由于移植受者数量的增加,EBV-PTLD的发生频率可能会上升,移植医生应意识到这种危及生命的并发症。对于U-CBT后发生EBV-PTLD和PRCA的患者,单独使用利妥昔单抗可能是一种有效的治疗策略。