进行性多灶性白质脑病并发那他珠单抗和干扰素β-1a治疗多发性硬化症。
Progressive multifocal leukoencephalopathy complicating treatment with natalizumab and interferon beta-1a for multiple sclerosis.
作者信息
Kleinschmidt-DeMasters B K, Tyler Kenneth L
机构信息
Department of Pathology, University of Colorado Health Sciences Center, Denver 80262, USA.
出版信息
N Engl J Med. 2005 Jul 28;353(4):369-74. doi: 10.1056/NEJMoa051782. Epub 2005 Jun 9.
A 46-year-old woman with relapsing-remitting multiple sclerosis died from progressive multifocal leukoencephalopathy (PML) after having received 37 doses of natalizumab (300 mg every four weeks) as part of a clinical trial of natalizumab and interferon beta-1a. PML was diagnosed on the basis of the finding of JC viral DNA in cerebrospinal fluid on polymerase-chain-reaction assay and was confirmed at autopsy. Nearly every tissue section from bilateral cerebral hemispheres contained either macroscopic or microscopic PML lesions. There was extensive tissue destruction and cavitation in the left frontoparietal area, large numbers of bizarre astrocytes, and inclusion-bearing oligodendrocytes, which were positive for JC virus DNA on in situ hybridization.
一名46岁复发缓解型多发性硬化症女性患者,在接受了37剂那他珠单抗(每四周300毫克)作为那他珠单抗和干扰素β-1a临床试验的一部分后,死于进行性多灶性白质脑病(PML)。PML是根据聚合酶链反应检测在脑脊液中发现JC病毒DNA而诊断的,并在尸检时得到证实。双侧大脑半球的几乎每个组织切片都含有肉眼可见或显微镜下可见的PML病变。左额顶叶区域有广泛的组织破坏和空洞形成,有大量奇异星形胶质细胞和含包涵体的少突胶质细胞,原位杂交显示这些细胞的JC病毒DNA呈阳性。