Neuromyelitis Optica Spectrum Disorder Associated with Cervical Spondylosis.

نویسندگان

  • Yuan Zhou
  • Lin Zhu
  • Hui-Lin Cheng
  • Yi-Xing Lin
چکیده

A 44‐year‐old woman was admitted to our hospital with a 10‐day history of ache of double upper limbs and numbness on the trunk below the chest and bilateral thighs. Ten days before, she had an onset of ache of double upper limbs without apparent inducement. At the same time, she developed trembling on hands when writing and numbness between the chest and bilateral knees, which were unable to be alleviated. At admission, she presented with hypoesthesia of superficial sensibility from bilateral costal margins to knees, positive bilateral Hoffman sign, and Babinski sign. Magnetic resonance imaging (MRI) [Figure 1a] of cervical vertebrae showed: (1) Cervical intervertebral disc herniation (C3–C7); (2) Intramedullary lesions with edema (C2–T2); (3) Cervical spondylolisthesis (C3–C5). She was admitted to our hospital with a presumptive diagnosis of cervical spondylosis and intramedullary lesions with edema (C2–T2). After admission, she was given dehydration, anti‐inflammatory, nerve nutrition, and symptomatic treatment immediately. Subsequent lumbar puncture showed results of cerebrospinal fluid routine were normal with normal protein, glucose, and chloride levels. Serum aquaporin‐4 (AQP‐4) antibody was tested by enzyme‐linked immunosorbent assay and showed positive. Also, visual evoked potential, brainstem auditory evoked potential, and somatosensory evoked potential were normal. All told that she was diagnosed as NMOSD as well as cervical spondylosis. Then, she received methylprednisolone (500 mg) impact therapy and sequential reduction of hormone therapy. Fifteen days later, MRI [Figure 1b] showed cervical and thoracic spinal cord lesions were significantly reduced. Her symptoms of upper limbs pain, numbness of chest, and abdomen had improved markedly and was discharged.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Tumefactive Brain Lesions in Patients with Neuromyelitis Optica Spectrum Disorder

Background: Neuromyelitis Optica Spectrum Disorder (NMOSD) is an autoimmune neurological disorder that is characterized by optic neuritis and longitudinally-extended transverse myelitis lesions in spinal segments. Magnetic Resonance Imaging (MRI) findings are part of the diagnostic process in NMOSD patients, and abnormal lesion patterns may cause deviation from a correct diagnosis.  Clinical P...

متن کامل

Association Between Helicobacter Pylori Infection and Seronegative Neuromyelitis Optica Spectrum Disorder

Background: Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disease in the central nervous system. Association between NMOSD and Helicobacter pylori (H. pylori) infection has been investigated, but few studies have assessed the relationship between H. pylori and seronegative AQP4-Ab NMOSD. Objectives: This study aimed to survey the association between H. pylori...

متن کامل

O 14: Differentiating Demyelinating Disorders of the Central Nervous System – a Focus on Multiple Sclerosis and Neuromyelitis-Optica Spectrum Disorders

Significant advances have been made in diagnosis and therapy of demyelinating disorders of the central nervous system. The most common entities of this disorders in adults – multiple sclerosis and neuromyelitis optica were initially thought to be different phenotypes of more or less the same disease. During the last ten years, this view was subsequently changed and the term neuromyelitis ...

متن کامل

Relapse of Neuromyelitis Optica Spectrum Disorder Associated with Intravenous Lidocaine

Lidocaine unmasks silent symptoms and eases neuropathic pain in multiple sclerosis patients; however, the effects of lidocaine in neuromyelitis optica have never been reported. We describe the case of a 59-year-old Japanese woman with neuromyelitis optica spectrum disorder who developed optic neuritis 1 day after intravenous lidocaine injection for treating allodynia. Her symptom seemed to resu...

متن کامل

Paroxysmal Chorea as a Relapse of Myelopathy in a Patient with Neuromyelitis Optica

Movement disorders secondary to intrinsic spinal cord disease are rare. Paroxysmal chorea has not yet been reported in the neuromyelitis optica (NMO). We report a 43-year-old woman with relapsing-remitting cervical myelopathy who developed paroxysmal chorea during clinical exacerbation of NMO. MRI scan of the cervical spine revealed a long segmental enhancing lesion, but brain MRI did not show ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Chinese medical journal

دوره 128 22  شماره 

صفحات  -

تاریخ انتشار 2015