[A case of treatment-related leukoencephalopathy during combination therapy with daratumumab, lenalidomide, and low-dose dexamethasone for multiple myeloma].

Q4 Medicine
Keiko Maezono-Kandori, Hiroki Suo, Naoki Tokuda, Atsushi Yamamoto, Shiori Ogura, Yoshinari Nagakane
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引用次数: 0

Abstract

A 75-year-old woman with multiple myeloma was admitted due to an acute disturbance of consciousness and aphasia two months after administration of daratumumab, lenalidomide and dexamethasone combination therapy (DLd therapy). Brain MRI on admission showed no acute ischemic changes. She was treated with antiepileptic drugs, and DLd therapy was discontinued, but her consciousness deteriorated, and follow-up brain MRI showed progressive FLAIR high-signal intensity lesions in the cerebral deep white matter bilaterally. Though methylprednisolone pulse therapy and high-dose intravenous immunoglobulin were ineffective, plasma exchange improved her consciousness, and she began to speak. In addition, her MRI findings improved. Progressive multifocal leukoencephalopathy induced by drugs for multiple myeloma has been reported, but, in this case, leukoencephalopathy associated with daratumumab was suspected because JC virus DNA was not detected in her cerebrospinal fluid.

[达拉单抗、来那度胺和小剂量地塞米松联合治疗多发性骨髓瘤期间发生治疗相关性白质脑病1例]。
一名75岁多发性骨髓瘤女性患者在接受达拉单抗、来那度胺和地塞米松联合治疗(DLd治疗)两个月后,因急性意识障碍和失语入院。入院时脑MRI未见急性缺血性改变。患者接受抗癫痫药物治疗,停用DLd治疗,但意识恶化,随访脑MRI示双侧脑深部白质进行性FLAIR高信号强度病变。虽然甲基强的松龙脉冲治疗和大剂量静脉注射免疫球蛋白无效,但血浆置换改善了她的意识,她开始说话。此外,她的MRI检查结果也有所改善。已有多发性骨髓瘤药物诱导的进行性多灶性脑白质病的报道,但在该病例中,由于脑脊液中未检测到JC病毒DNA,因此怀疑与达拉单抗相关的脑白质病。
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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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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