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Concurrent aquaporin-4-positive NMOSD and neurosyphilis: A case report.
Chen, Hua-Qiu; Zhang, Ying; Wang, Si-Bo; Song, Yan-Na; Bai, Miao-Shui; Liu, Kang-Ding; Zhu, Ming-Qin.
Affiliation
  • Chen HQ; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China.
  • Zhang Y; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China.
  • Wang SB; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China.
  • Song YN; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China.
  • Bai MS; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China.
  • Liu KD; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China. Electronic address: kangdingliu@163.com.
  • Zhu MQ; Department of Neurology and Neuroscience Center, First Hospital of Jilin University, Xinmin Street No71, Changchun 130000, China. Electronic address: Mingqin.Zhu@hotmail.com.
Mult Scler Relat Disord ; 34: 137-140, 2019 Sep.
Article in En | MEDLINE | ID: mdl-31272070
ABSTRACT
Neuromyelitis optica spectrum disorder (NMOSD) is a common neuroinflammatory demyelinating disease associated with aquaporin-4 (AQP4) antibody in the central nervous system. Neurosyphilis is a neurological disease caused by Treponema pallidum infection. NMOSD commonly occurs concurrently with autoimmune diseases. However, they have rarely been associated with infectious diseases. In this report we describe a rare case of concurrent AQP4-positive NMOSD and neurosyphilis. A 60-year-old man was admitted to our hospital with a complaint of progressive weakness in his legs for one month. T2-weighted magnetic resonance images of the spinal cord showed longitudinal extensive lesions at C7-T7. The rapid plasma reagin test and T. pallidum particle agglutination assay performed using patient serum and cerebrospinal fluid (CSF) were positive. Additionally, the AQP4-immunoglobulin (Ig) G was detected in the serum and CSF. The patient's symptom gradually improved after penicillin and methylprednisolone treatment. This case report highlights the possibility of the presence of an infectious disease in patients with NMOSD.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neuromyelitis Optica / Aquaporin 4 / Neurosyphilis Type of study: Diagnostic_studies Limits: Humans / Male / Middle aged Language: En Journal: Mult Scler Relat Disord Year: 2019 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neuromyelitis Optica / Aquaporin 4 / Neurosyphilis Type of study: Diagnostic_studies Limits: Humans / Male / Middle aged Language: En Journal: Mult Scler Relat Disord Year: 2019 Document type: Article Affiliation country: China
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