利妥昔单抗、甲氨蝶呤、丙卡嗪和长春新碱治疗颅内甲氨蝶呤相关淋巴增生性疾病无eb病毒感染1例

NMC Case Report Journal Pub Date : 2022-07-27 eCollection Date: 2022-01-01 DOI:10.2176/jns-nmc.2022-0091
Makoto Mizushima, Yukitomo Ishi, Hiroshi Ikeda, Ikuma Echizenya, Takuya Otsuka, Tomoko Mitsuhashi, Shigeru Yamaguchi, Miki Fujimura
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引用次数: 2

摘要

甲氨蝶呤相关淋巴细胞增生性疾病(MTX- lpd)发生在接受甲氨蝶呤(MTX)治疗的类风湿性关节炎(RA)患者中。MTX- lpd通常与eb病毒(EBV)感染相关,并随MTX停药而消退。另一方面,ebv阴性的MTX- lpd不太常见,更有可能在MTX停药后显示部分或没有恢复。对于难治性MTX-LPD没有标准的化疗选择。我们报告了一例ebv阴性中枢神经系统(CNS) MTX-LPD患者,该患者成功地使用利妥昔单抗、甲氨蝶呤、丙卡嗪和长春新碱(R-MPV)治疗,然后采用与原发性中枢神经系统淋巴瘤相同的治疗方案进行低剂量全脑放疗(rdWBRT)。一位59岁女性RA患者接受甲氨蝶呤治疗后,表现为逐渐发展为步履蹒跚、记忆缺陷和定向障碍。在脑磁共振成像中发现多发病变,并伴有不均匀增强。患者被怀疑患有MTX- lpd,但停用MTX并没有导致脑部病变的消退。她接受了左顶叶病变活检。病理诊断为弥漫性大b细胞淋巴瘤。此外,通过EBV编码核糖核酸原位杂交的病理检查显示没有EBV感染。她最终被诊断为ebv阴性中枢神经系统MTX-LPD。我们采用R-MPV和rdWBRT联合化疗。病人完全痊愈了。对于没有EBV感染的CNS MTX-LPD,可以考虑R-MPV化疗后再进行rdWBRT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Successful Treatment of Intracranial Methotrexate-associated Lymphoproliferative Disorder without Epstein-Barr Virus Infection Using Rituximab, Methotrexate, Procarbazine, and Vincristine: A Case Report.

Methotrexate-associated lymphoproliferative disorder (MTX-LPD) occurs in patients with rheumatoid arthritis (RA) treated with methotrexate (MTX). MTX-LPD is typically associated with Epstein-Barr virus (EBV) infection and regresses with MTX discontinuation. On the other hand, EBV-negative MTX-LPDs are less common and are more likely to show partial or no regression after MTX discontinuation. There were no standard chemotherapeutic options for refractory MTX-LPD. We present a case of EBV-negative MTX-LPD in the central nervous system (CNS) that was successfully treated with rituximab, methotrexate, procarbazine, and vincristine (R-MPV), followed by reduced-dose whole-brain radiotherapy (rdWBRT), following the same treatment protocol as primary CNS lymphoma. A 59-year-old woman with RA treated with MTX presented with gradually developing staggered gait, memory deficit, and disorientation. Multiple lesions with heterogeneous contrast enhancement were discovered using brain magnetic resonance imaging. The patient was suspected of having MTX-LPD, but discontinuing MTX did not result in regression of the brain lesions. She underwent a biopsy from the left parietal lesion. The tissue was pathologically diagnosed as diffuse large B-cell lymphoma. Furthermore, pathological examination through EBV-encoded ribonucleic acid in situ hybridization demonstrated a lack of EBV infection. She was ultimately diagnosed with EBV-negative CNS MTX-LPD. We applied chemotherapy with R-MPV and rdWBRT. The patient achieved a complete response. In the case of CNS MTX-LPD without EBV infection, chemotherapy with R-MPV followed by rdWBRT may be considered.

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