Literature DB >> 26359279

Progressive cerebral atrophy in neuromyelitis optica.

Yoko Warabi1, Toshiyuki Takahashi2, Eiji Isozaki3.   

Abstract

We report two cases of neuromyelitis optica patients with progressive cerebral atrophy. The patients exhibited characteristic clinical features, including elderly onset, secondary progressive tetraparesis and cognitive impairment, abnormally elevated CSF protein and myelin basic protein levels, and extremely highly elevated serum anti-AQP-4 antibody titer. Because neuromyelitis optica pathology cannot switch from an inflammatory phase to the degenerative phase until the terminal phase, neuromyelitis optica rarely appears as a secondary progressive clinical course caused by axonal degeneration. However, severe intrathecal inflammation and massive destruction of neuroglia could cause a secondary progressive clinical course associated with cerebral atrophy in neuromyelitis optica patients.
© The Author(s), 2015.

Entities:  

Keywords:  Multiple sclerosis; anti-aquaporin-4 antibody; astrocyte; axonal degeneration; inflammation; neuromyelitis optica; progressive cerebral atrophy; secondary progressive

Mesh:

Year:  2015        PMID: 26359279     DOI: 10.1177/1352458515600246

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  1 in total

1.  Foveal thinning in neuromyelitis optica: A sign of retinal astrocytopathy?

Authors:  Takashi Yamamura; Ichiro Nakashima
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2017-04-11
  1 in total

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