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类风湿关节炎免疫抑制治疗后发生的爱泼斯坦-巴尔病毒阳性多发性骨髓瘤:一例报告并文献复习

Epstein-Barr virus-positive multiple myeloma developing after immunosuppressant therapy for rheumatoid arthritis: a case report and review of literature.

作者信息

Sekiguchi Yasunobu, Shimada Asami, Ichikawa Kunimoto, Wakabayashi Mutsumi, Sugimoto Keiji, Ikeda Keigo, Sekikawa Iwao, Tomita Shigeki, Izumi Hiroshi, Nakamura Noriko, Sawada Tomohiro, Ohta Yasunori, Komatsu Norio, Noguchi Masaaki

机构信息

Department of Hematology, Juntendo University Urayasu Hospital Japan.

Department of Hematology, Juntendo University Urayasu Hospital Japan ; Division of Pathology, Research Hospital, Institute of Medical Science, University of Tokyo Japan.

出版信息

Int J Clin Exp Pathol. 2015 Feb 1;8(2):2090-102. eCollection 2015.

Abstract

A 61-year-old woman was diagnosed as having rheumatoid arthritis (RA) and began treatment with salazosulfapyridine (SASP) and methotrexate (MTX) in 2008; the administration of concomitant tacrolimus (TAC) was initiated in 2010. She subsequently developed concurrent multiple myeloma (MM), immunoglobulin G (IgG)-κ type, in 2012. A portion of the tumor cells tested positive for Epstein-Barr virus-encoded small RNA (EBER). MTX treatment was discontinued in 2014, and the exacerbation of MM ensued. The patient received two cycles of bortezomib plus dexamethasone (BD) therapy and attained a complete response (CR). She then underwent an autologous peripheral blood stem cell transplantation. The Epstein-Barr (EB) virus infection arising from the increased RA disease activity and immunosuppressant medication might have influenced the development of MM in this case. Most reported patients with EB virus-positive plasmacytoma are in a state of immunosuppression, and this condition may fall within the category of other iatrogenic immunodeficiency-associated lymphoproliferative disorders. No other reports of plasmacytoma occurring in a background of RA or after TAC or MTX therapy have been made, and the present case is the first such report.

摘要

一名61岁女性于2008年被诊断为类风湿关节炎(RA),并开始使用柳氮磺胺吡啶(SASP)和甲氨蝶呤(MTX)进行治疗;2010年开始同时使用他克莫司(TAC)。她随后于2012年并发多发性骨髓瘤(MM),免疫球蛋白G(IgG)-κ型。部分肿瘤细胞检测到爱泼斯坦-巴尔病毒编码的小RNA(EBER)呈阳性。2014年停用MTX治疗,随后MM病情加重。患者接受了两个周期的硼替佐米联合地塞米松(BD)治疗并获得完全缓解(CR)。然后她接受了自体外周血干细胞移植。在该病例中,由RA疾病活动增加和免疫抑制药物引起的爱泼斯坦-巴尔(EB)病毒感染可能影响了MM的发生。大多数报告的EB病毒阳性浆细胞瘤患者处于免疫抑制状态,这种情况可能属于其他医源性免疫缺陷相关的淋巴增殖性疾病范畴。此前尚无关于在RA背景下或TAC或MTX治疗后发生浆细胞瘤的其他报告,本病例为首例此类报告。

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