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. Author manuscript; available in PMC: 2018 Oct 15.
Published in final edited form as: J Neurol Sci. 2017 Aug 10;381:83–87. doi: 10.1016/j.jns.2017.08.015

Table 1.

Non-malignant brain biopsy-confirmed inflammatory-demyelination: Study Cohort

Demographics (n=29)

  Age in years, mean (Range) 41.4 (16–69)

  Sex (%female) 51.7%

  Race/Ethnicity

    Caucasian 13 (44.8%)

    Asian 6 (20.7%)

    Black 2 (6.9%)

    Other/Unknown 8 (27.6%)

Clinical History

  Prior Demyelination Events 3 (10.3%)

  Prior Neurologic History* 8 (27.6%)

Radiographic Features

  Lesion Number

    Solitary 12 (41.4%)

    Multifocal 17 (58.6%)

  Edema 23 (79.3%)

  Enhancement 28 (96.6%)

    Incomplete Rim 22 (75.9%)

    Nodular 4 (13.8%)

    Patchy 2 (6.9%)

    Radiating/Linear 2 (6.9%)

    Complete Rim 1 (3.4%)

  Spinal Lesions (n=24) 6 (25%)
Laboratory Features
  Serum anti-AQP4 IgG (n=13) 0 (0%)

Treatment

  Glucocorticoids 20 (69.0%)

  Plasma Exchange 14 (48.1%)

  Immunosuppressive therapy (n=21) 15 (71.4%)

Prognosis

  Follow-up duration, months (median) 22

  Clinical Relapse

    All Subjects# 8 (40%)

    ≥12 months follow-up (n=16) 7 (43.8%)

  MRI Progression (n=22)

    All Subjects 9 (40.9%)

    ≥12 months follow-up (n=16) 6 (37.5%)

    Recurrent TDL 3 (13.6%)

  Last EDSS, mean (SD) 3.5 (2.4)
*

Prior Neurological History included suspected stroke (n=1), seizure disorder (n=3), autoimmune encephalitis (n=1), facial palsy (n=1), paraparesis (n=1), optic neuritis (n=1).

#

20 patients with available follow-up.