Guo Hanguo, Zhang Hong, Li Wenyu
Department of Lymphoma, Guangdong Academy of Medical Sciences, Guangdong Provincial People's Hospital, Southern Medical University, 106 Zhongshan Er Rd, Guangzhou, 510080, Guangdong, China.
J Med Case Rep. 2025 May 21;19(1):244. doi: 10.1186/s13256-025-05307-x.
Post-transplant lymphoproliferative disorder and methotrexate-related lymphoproliferative disorder are rare complications normally with unfavorable prognosis. Post-transplant lymphoproliferative disorder of the central nervous system is a rare disorder and predominantly presents as diffuse large B-cell lymphomas of non-germinal center cell origin. However, the treatment for these patients with this diagnosis has not reached a consensus. CASE 1 AND 2 PRESENTATIONS: In this case report, one patient with post-transplant lymphoproliferative disorder and another patient with methotrexate-related lymphoproliferative disorder were both diagnosed with Epstein-Barr virus-diffuse large B-cell lymphomas of primary central nervous system. The former case was a 37-year-old Han Chinese female diagnosed with post-transplant lymphoproliferative disorder of the central nervous system after a kidney transplant, and the latter case was a 61-year-old Han Chinese male diagnosed with methotrexate-related lymphoproliferative disorder after receiving methotrexate treatment for psoriasis. The initial treatment for both of them was rituximab plus lenalidomide followed by lenalidomide as maintenance for disease progression or intolerance. After the treatment, magnetic resonance imaging showed partial response or complete remission of their brain lesions. In addition, the renal function of the patient with post-transplant lymphoproliferative disorder of the central nervous system was normal, and psoriasis did not recur in the patient with methotrexate-related lymphoproliferative disorder during lenalidomide maintenance treatment.
The treatment has proved to be a promising therapeutic method for post-transplant lymphoproliferative disorder of the central nervous system and methotrexate-related lymphoproliferative disorder, when the decreasing or withdrawal of immunosuppressive therapy could not achieve a satisfying outcome. Owing to the relatively small sample size, the effect of this treatment should be further investigated under a larger sample size.
移植后淋巴组织增生性疾病和甲氨蝶呤相关淋巴组织增生性疾病是罕见的并发症,通常预后不佳。中枢神经系统移植后淋巴组织增生性疾病是一种罕见疾病,主要表现为非生发中心细胞起源的弥漫性大B细胞淋巴瘤。然而,对于这些诊断为该病的患者的治疗尚未达成共识。
病例1和病例2介绍:在本病例报告中,一名移植后淋巴组织增生性疾病患者和另一名甲氨蝶呤相关淋巴组织增生性疾病患者均被诊断为原发性中枢神经系统爱泼斯坦-巴尔病毒弥漫性大B细胞淋巴瘤。前一例是一名37岁的汉族女性,肾移植后被诊断为中枢神经系统移植后淋巴组织增生性疾病,后一例是一名61岁的汉族男性,因银屑病接受甲氨蝶呤治疗后被诊断为甲氨蝶呤相关淋巴组织增生性疾病。他们两人的初始治疗均为利妥昔单抗加利奈利德,随后在疾病进展或不耐受时以来那度胺维持治疗。治疗后,磁共振成像显示他们脑部病变部分缓解或完全缓解。此外,中枢神经系统移植后淋巴组织增生性疾病患者的肾功能正常,在来那度胺维持治疗期间,甲氨蝶呤相关淋巴组织增生性疾病患者的银屑病未复发。
当免疫抑制治疗的减量或停用不能取得满意疗效时,该治疗方法已被证明是治疗中枢神经系统移植后淋巴组织增生性疾病和甲氨蝶呤相关淋巴组织增生性疾病的一种有前景的治疗方法。由于样本量相对较小,该治疗方法的效果应在更大样本量下进一步研究。