Imaging Aspects of Neuromyelitis Optica: A Case Study and Literature Review

Understanding Neuromyelitis Optica: Case Summary A recent case report highlights a 19-year-old male diagnosed with NMOSD. The patient presented with tetraparesis and bilateral blindness, which progressed over five months. Brain and spinal cord MRI findings revealed:

  • Bilateral optic neuropathy
  • Signal hyperintensities at the medulla oblongata, cervical, and thoracic spinal cord (T2-weighted sequence)
  • Longitudinally extensive spinal cord lesions spanning three vertebral segments
  • No gadolinium enhancement on imaging

Despite negative NMO IgG results in cerebrospinal fluid analysis, the patient was diagnosed with NMOSD and responded favorably to methylprednisolone treatment, with symptoms resolving over time.

Radiological Features of NMOSD MRI plays a crucial role in distinguishing NMOSD from multiple sclerosis (MS) and other inflammatory CNS conditions. Key imaging findings include:

  • Optic Nerve and Chiasm: Bilateral optic nerve involvement with hyperintensities on T2-weighted sequences and enhancement on T1-weighted imaging in acute cases.
  • Spinal Cord: Longitudinally extensive transverse myelitis (LETM) spanning three or more vertebral segments, predominantly affecting the central gray matter.
  • Brain Involvement: Although NMOSD was traditionally considered to spare the brain, recent studies indicate asymmetrical hyperintensities in periependymal areas, corpus callosum, and brainstem.

Additional Resources and Related Studies For further reading on NMOSD and its imaging characteristics, explore our collection of case reports and articles on CNS disorders at https://www.clinmedcasereportsjournal.com/acr. A detailed analysis can also be found in our main journal article here.

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