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Inflammatory disorder involving both halves of spinal cord, resulting in bilateral motor, sensory, and autonomic dysfunction
Central cord expansile lesion > 2 vertebral segments in length ± variable eccentric enhancement
Multiple sclerosis
Neuromyelitis optica
Spinal cord neoplasm
Spinal cord infarction
Autoimmune phenomenon with formation of antigen-antibody complexes
Small vessel vasculopathy → cord ischemia
Associated demyelinating process
Inclusion criteria
Sensory, motor, or autonomic dysfunction (including bowel/bladder involvement) attributable to spinal cord
Bilateral signs/symptoms with well-defined sensory level
Compressive etiology excluded by neuroimaging
Cord inflammation confirmed by cerebrospinal fluid pleocytosis, elevated IgG index, or gadolinium enhancement
Exclusion criteria
History of spinal radiation within past 10 years
Cord ischemia/infarction, arteriovenous malformation
Connective tissue diseases
CNS infections, sarcoidosis, SLE, or Sjögren syndrome
Central cord lesion > 2 vertebra in length, eccentric enhancement → consider acute transverse myelitis
More focal cord T2 hyperintensity, enhancement → more characteristic of multiple sclerosis
Idiopathic acute transverse myelitis (IATM)
Idiopathic transverse myelopathy
Inflammatory disorder involving both halves of spinal cord, resulting in bilateral motor, sensory, and autonomic dysfunction
Pathogenetically heterogeneous inflammatory disorder of spinal cord
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