Division of Hematology/Oncology, Department of Internal Medicine, Kameda Medical Center, 929 Higashi-chou, Kamogawa, Chiba, 296-8602, Japan.
Int J Hematol. 2021 Jul;114(1):136-140. doi: 10.1007/s12185-021-03111-z. Epub 2021 Mar 6.
Here, we describe the case of a male patient with Epstein-Barr virus post-transplantation lymphoproliferative disorder (EBV-PTLD), which developed 18 months after a haploidentical hematopoietic stem cell transplantation (haplo-HSCT) and the administration of post-transplant cyclophosphamide (PTCy). Of note, no anti-thymoglobulin was used in the entire clinical course. Prior to the onset of EBV-PTLD, the patient had pulmonary chronic graft-versus-host disease and was treated with prednisolone and tacrolimus. After stopping immunosuppressive therapy, he was diagnosed with EBV-positive infectious mononucleosis PTLD, and EBV-associated hemophagocytic syndrome; therefore, dexamethasone and rituximab monotherapies were administered. After four courses of rituximab, EBV-DNA was no longer detected in the peripheral blood, and the patient's laboratory data improved. Overall, this study highlights the need to predict the risk factors associated with the development of EBV-PTLD in transplanted patients after haplo-HSCT with PTCy.
在这里,我们描述了一例男性患者在接受单倍体造血干细胞移植(haplo-HSCT)和使用移植后环磷酰胺(PTCy)后 18 个月发生 EBV 移植后淋巴组织增殖性疾病(EBV-PTLD)的情况。值得注意的是,在整个临床过程中没有使用抗胸腺球蛋白。在 EBV-PTLD 发病前,患者患有肺部慢性移植物抗宿主病,并接受了泼尼松龙和他克莫司治疗。停止免疫抑制治疗后,他被诊断为 EBV 阳性传染性单核细胞增多症 PTLD 和 EBV 相关噬血细胞综合征,因此给予地塞米松和利妥昔单抗单药治疗。四疗程利妥昔单抗后,外周血中不再检测到 EBV-DNA,患者的实验室数据得到改善。总之,本研究强调了需要预测在接受 haplo-HSCT 加 PTCy 治疗的移植患者中发生 EBV-PTLD 的相关危险因素。