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一名弥漫性大B细胞淋巴瘤患者在接受利妥昔单抗和CHOP化疗期间发生进行性多灶性白质脑病。

Progressive multifocal leukoencephalopathy during treatment with rituximab and CHOP chemotherapy in a patient with a diffuse large B-cell lymphoma.

作者信息

Sikkema Tineke, Schuiling Wouter Jan, Hoogendoorn Mels

机构信息

Department of Neurology, Medical Centre Leeuwarden, Leeuwarden, Friesland, The Netherlands.

出版信息

BMJ Case Rep. 2013 Jan 25;2013:bcr2012008142. doi: 10.1136/bcr-2012-008142.

Abstract

A 74-year-old woman with a diffuse large B-cell lymphoma was treated with rituximab and CHOP chemotherapy. After three cycles of chemotherapy she developed progressive symptoms of motor imbalance, fatigue, weight loss and impaired cognitive function, which was interpreted as toxicity of the CHOP chemotherapy. The sixth cycle CHOP chemotherapy was withheld and three additional cycles of rituximab were given. Two weeks later, neurological symptoms appeared, including abducens nerve palsy of her left eye, ataxia and hemiparesis of her right body. MRI of the brain revealed two hyperintense lesions on T2-weighted and fluid-attenuated inversion recovery images without oedema or gadolinium enhancement. A PCR on John Cunningham (JC) virus DNA in cerebrospinal fluid was negative, but subsequent brain biopsy diagnosed progressive multifocal leukoencephalopathy (PML). She rapidly deteriorated and died. Awareness of PML during immunosuppressive therapy can be lifesaving, since only immune reconstitution can prevent mortality in these patients.

摘要

一名74岁的弥漫性大B细胞淋巴瘤女性患者接受了利妥昔单抗和CHOP化疗。化疗三个周期后,她出现了进行性运动失衡、疲劳、体重减轻和认知功能受损等症状,这些症状被认为是CHOP化疗的毒性反应。于是停止了第六周期的CHOP化疗,并额外进行了三个周期的利妥昔单抗治疗。两周后,出现了神经症状,包括左眼外展神经麻痹、共济失调和右侧身体偏瘫。脑部MRI显示,在T2加权像和液体衰减反转恢复图像上有两个高信号病变,无水肿或钆增强。脑脊液中约翰·坎宁安(JC)病毒DNA的聚合酶链反应(PCR)结果为阴性,但随后的脑活检诊断为进行性多灶性白质脑病(PML)。她病情迅速恶化并死亡。在免疫抑制治疗期间意识到PML可能会挽救生命,因为只有免疫重建才能防止这些患者死亡。

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