Division of Neuro-Immunology Departments of Neurology and Medicine Center for Virology and Vaccine Research Beth Israel Deaconess Medical Center Harvard Medical School Boston Massachusetts.
Division of General Medicine and Primary Care Section for Research Department of Medicine Beth Israel Deaconess Medical Center Harvard Medical School Boston Massachusetts.
Ann Clin Transl Neurol. 2016 Apr 6;3(5):386-91. doi: 10.1002/acn3.301. eCollection 2016 May.
We investigated delay in diagnosing progressive multifocal leukoencephalopathy (PML). The median time from initial symptom to diagnosis was 74 days (range 1-1643) in 111 PML patients seen at our institution from 1993 to 2015. Another diagnosis was considered before PML in nearly two-thirds, and more than three-quarters of patients suffered from diagnostic delay greater than 1 month, irrespective of their underlying immunosuppressive condition. Extended diagnostic delay occurred more frequently in patients with possible PML, and among HIV (+) patients with higher CD4(+) T-cell counts at symptom onset. Prompt diagnosis may improve survival of PML in so far as immune reconstitution can be effected, and prevent unnecessary interventions.
我们研究了进行性多灶性白质脑病(PML)的诊断延迟情况。在我们医院,1993 年至 2015 年间,共收治了 111 名 PML 患者,从首发症状到确诊的中位时间为 74 天(范围 1-1643 天)。在这些患者中,将近三分之二的患者在确诊 PML 之前曾被误诊,超过四分之三的患者的诊断延迟超过 1 个月,而与他们潜在的免疫抑制状况无关。在可能的 PML 患者和在症状发作时 CD4(+)T 细胞计数较高的 HIV(+)患者中,更常出现较长的诊断延迟。只要能够进行免疫重建,及时诊断可能会改善 PML 的生存状况,并防止不必要的干预。