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临床无症状的 PML 和多发性硬化症患者接受那他珠单抗治疗后的免疫重建炎症综合征延长。

Clinically silent PML and prolonged immune reconstitution inflammatory syndrome in a patient with multiple sclerosis treated with natalizumab.

机构信息

Danish Multiple Sclerosis Center, Department of Neurology, Copenhagen University Hospital, Rigshospitalet, Denmark.

出版信息

Mult Scler. 2013 Aug;19(9):1226-9. doi: 10.1177/1352458513481010. Epub 2013 Mar 18.

Abstract

We report the case of a woman with natalizumab-treated multiple sclerosis (MS) and clinically silent progressive multifocal leukoencephalopathy (PML) with an unusually long preclinical phase, followed by acute symptoms due to development of immune reconstitution inflammatory syndrome (IRIS). Furthermore, the course of the IRIS was prolonged and continued to progress even five months after natalizumab treatment was ceased. This case shows that PML and IRIS can have a considerably variable course in natalizumab-treated MS patients and underlines the need for PML screening in JC virus antibody-positive patients in order to detect clinically silent cases.

摘要

我们报告了一例患有那他珠单抗治疗的多发性硬化症(MS)和临床无症状进行性多灶性白质脑病(PML)的女性病例,其具有异常长的临床前期,随后由于免疫重建炎症综合征(IRIS)的发展而出现急性症状。此外,IRIS 的病程延长,即使在停止那他珠单抗治疗五个月后仍继续进展。该病例表明,PML 和 IRIS 在接受那他珠单抗治疗的 MS 患者中可能具有相当多变的病程,并强调了在 JC 病毒抗体阳性患者中进行 PML 筛查的必要性,以便检测临床无症状病例。

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