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下颌骨坏死患者的甲氨蝶呤相关淋巴增殖性疾病:3例报告及文献综述

Methotrexate-Related Lymphoproliferative Disorder in Patients With Osteonecrosis of the Jaw: A 3-Case Report and Literature Review.

作者信息

Furudate Ken, Satake Anna, Narita Norihiko, Kobayashi Wataru

机构信息

Chief, Department of Oral and Maxillofacial Surgery, Tsugaru General Hospital, Goshogawara; Visiting Fellow, Department of Oral and Maxillofacial Surgery, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Graduate Student, Department of Oral and Maxillofacial Surgery, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

出版信息

J Oral Maxillofac Surg. 2018 Jan;76(1):97-111. doi: 10.1016/j.joms.2017.05.027. Epub 2017 Jun 1.

Abstract

Patients with immunodeficiency or immunosuppression are at risk of developing a lymphoproliferative disorder (LPD). Methotrexate (MTX) is an iatrogenic cause of LPD, which in up to 50% cases occurs in extranodal sites. The occurrence of MTX-related LPD with osteonecrosis of the jaw (ONJ) has rarely been reported. Moreover, there are no clear diagnostic criteria and treatment strategies for management of these lesions. In the present cases, discontinuing MTX and debridement of the necrotic bone were effective. This report describes 3 cases of MTX-related LPD in patients with longstanding rheumatoid arthritis (RA) who presented with ONJ. The first patient was a 74-year-old man with RA who had received treatment with MTX for 7 years before presenting with ONJ and submental lymphadenopathy. The second patient was a 79-year-old woman who had been treated for 21 years with MTX and who presented with ONJ. The third patient was a 67-year-old man who had been treated with MTX for more than 15 years. In all 3 cases, biopsy, histology, and immunohistochemistry using a panel of lymphoid markers (Epstein-Barr virus [EBV], CD79a, CD20, PAX-5, CD3, and CD30) resulted in the diagnosis of EBV-driven T-cell, B-cell, and Hodgkin-like LPD. All 3 patients recovered after cessation of MTX and surgical debridement. Biopsy examination, diagnostic immunohistochemistry using lymphoid immune markers, and imaging studies using computed tomography, magnetic resonance imaging, and positron-emission tomographic computed tomography were useful for the correct diagnosis of this condition.

摘要

免疫缺陷或免疫抑制患者有发生淋巴增殖性疾病(LPD)的风险。甲氨蝶呤(MTX)是LPD的医源性病因,高达50%的病例发生在结外部位。MTX相关LPD合并颌骨骨坏死(ONJ)的情况鲜有报道。此外,对于这些病变的管理,尚无明确的诊断标准和治疗策略。在本病例中,停用MTX和坏死骨清创术有效。本报告描述了3例长期类风湿关节炎(RA)患者发生MTX相关LPD并伴有ONJ的病例。首例患者为一名74岁男性RA患者,在出现ONJ和颏下淋巴结病之前接受MTX治疗7年。第二例患者为一名79岁女性,接受MTX治疗21年,出现ONJ。第三例患者为一名67岁男性,接受MTX治疗超过15年。在所有3例病例中,通过活检、组织学检查以及使用一组淋巴标志物(爱泼斯坦-巴尔病毒[EBV]、CD79a、CD20、PAX-5、CD3和CD30)进行免疫组织化学检查,确诊为EBV驱动的T细胞、B细胞和霍奇金样LPD。所有3例患者在停用MTX和手术清创后均康复。活检检查、使用淋巴免疫标志物的诊断性免疫组织化学检查以及使用计算机断层扫描、磁共振成像和正电子发射断层扫描计算机断层扫描的影像学检查,有助于对这种疾病进行正确诊断。

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