Department of Biomedicine and Neurology, University Hospital Basel, Basel, Switzerland.
Neurology. 2011 Dec 6;77(23):2010-6. doi: 10.1212/WNL.0b013e31823b9b27. Epub 2011 Nov 9.
To describe the diagnosis and management of a 49-year-old woman with multiple sclerosis (MS) developing a progressive hemiparesis and expanding MRI lesion suspicious of progressive multifocal leukoencephalopathy (PML) 19 months after starting natalizumab.
Polyomavirus JC (JCV)-specific qPCR in CSF was repeatedly negative, but JCV-specific antibodies indicated intrathecal production. Brain biopsy tissue taken 17 weeks after natalizumab discontinuation and plasmapheresis was positive for JCV DNA with characteristic rearrangements of the noncoding control region, but histology and immunohistochemistry were not informative except for pathologic features compatible with immune reconstitution inflammatory syndrome. A total of 22 months later, the clinical status had returned close to baseline level paralleled by marked improvement of neuroradiologic abnormalities.
This case illustrates diagnostic challenges in the context of incomplete suppression of immune surveillance and the potential of recovery of PML associated with efficient immune function restitution.
描述一位 49 岁女性多发性硬化症(MS)患者的诊断和治疗情况,该患者在开始使用那他珠单抗 19 个月后出现进行性偏瘫和扩大的 MRI 病变,疑似进展性多灶性白质脑病(PML)。
CSF 中多瘤病毒 JC(JCV)特异性 qPCR 反复为阴性,但 JCV 特异性抗体表明存在鞘内产生。在停止那他珠单抗和血浆置换后 17 周时进行的脑活检组织中,JCV DNA 呈阳性,具有非编码控制区特征性重排,但组织学和免疫组织化学除了与免疫重建炎症综合征相符的病理特征外,没有提供信息。22 个月后,临床状况已接近基线水平,神经影像学异常明显改善。
本例说明了在免疫监测不完全抑制的情况下进行诊断的挑战,以及与有效免疫功能恢复相关的 PML 恢复的可能性。