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Acute combined central and peripheral demyelination showing anti-aquaporin 4 antibody positivity.

Abstract
Neuromyelitis optica spectrum disorder (NMOSD) is characterized by optic neuritis or transverse myelitis with anti-aquaporin 4 (AQP4) antibodies (1). We herein present the case of a patient with NMOSD who also was affected with peripheral neuropathy. A 58-year-old woman developed gait disturbance and sensory impairment in the lower limbs. She exhibited longitudinally extensive transverse myelitis with anti-AQP4 antibodies. Nerve conduction studies showed demyelinating changes. Laboratory findings showed hepatitis-C virus (HCV) infection. Her peripheral neuropathy improved after immunotherapy. There have been no previous reports of NMO or NMOSD associated with neuropathy. The HCV infection or undetermined humoral factors other than the anti-AQP4 antibodies may have caused her peripheral neuropathy.
AuthorsMari Kitada, Hidekazu Suzuki, Juri Ichihashi, Rino Inada, Katsuichi Miyamoto, Toshiyuki Takahashi, Yoshiyuki Mitsui, Kazuo Fujihara, Susumu Kusunoki
JournalInternal medicine (Tokyo, Japan) (Intern Med) Vol. 51 Issue 17 Pg. 2443-7 ( 2012) ISSN: 1349-7235 [Electronic] Japan
PMID22975565 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Anti-Idiotypic
  • Aquaporin 4
  • Carbamazepine
  • Prednisolone
  • Methylprednisolone
Topics
  • Acute Disease
  • Antibodies, Anti-Idiotypic (blood)
  • Aquaporin 4 (immunology)
  • Carbamazepine (therapeutic use)
  • Comorbidity
  • Female
  • Humans
  • Methylprednisolone (therapeutic use)
  • Middle Aged
  • Neuromyelitis Optica (drug therapy, epidemiology, immunology)
  • Peripheral Nervous System Diseases (drug therapy, epidemiology, immunology)
  • Prednisolone (therapeutic use)
  • Treatment Outcome

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