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Neuroimaging characteristics of neuromyelitis optica spectrum disorders

Neuroimaging characteristics of neuromyelitis optica spectrum disorders
Spinal cord MRI, acute
LETM lesion associated with acute TM
Increased signal on sagittal T2-weighted (standard T2-weighted, proton density, or STIR sequences) extending over three or more complete vertebral segments
Central cord predominance (more than 70% of the lesion residing within the central gray matter)
Gadolinium enhancement of the lesion on T1-weighted sequences (no specific distribution or pattern of enhancement is required)
Other characteristic features that may be detected
Rostral extension of the lesion into the brainstem
Cord expansion/swelling
Decreased signal on T1-weighted sequences corresponding to region of increased T2-weighted signal
Spinal cord MRI, chronic
Longitudinally extensive cord atrophy (sharply demarcated atrophy extending over ≥3 complete, contiguous vertebral segments and caudal to a particular segment of the spinal cord), with or without focal or diffuse T2 signal change involving the atrophic segment
Optic nerve MRI
Unilateral or bilateral increased T2 signal or T1 gadolinium enhancement within optic nerve or optic chiasm; relatively long lesions (eg, those extending more than half the distance from orbit to chiasm) and those involving the posterior aspects of the optic nerves or the chiasm are associated with NMO
Cerebral MRI: NMOSD-typical brain lesion patterns (increased signal on T2-weighted MRI sequences unless otherwise noted)
Lesions involving the dorsal medulla (especially the area postrema), either small and localized, often bilateral, or contiguous with an upper cervical spinal cord lesion
Periependymal surfaces of the fourth ventricle in the brainstem/cerebellum
Lesions involving the hypothalamus, thalamus, or periependymal surfaces of the third ventricle
Large, confluent, unilateral, or bilateral subcortical or deep white matter lesions
Long (one-half of the length of the corpus callosum or greater), diffuse, heterogeneous, or edematous corpus callosum lesions
Long corticospinal tract lesions, unilateral or bilateral, contiguously involving internal capsule and cerebral peduncle
Extensive periependymal brain lesions, often with gadolinium enhancement
LETM: longitudinally extensive transverse myelitis lesions; TM: transverse myelitis; NMOSD: neuromyelitis optica spectrum disorders; NMO: neuromyelitis optica; STIR: short tau inversion recovery.
From: Wingerchuk DM, Banwell B, Bennett JL, et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology 2015; 85:177. DOI: 10.1212/WNL.0000000000001729. Copyright © 2015 American Academy of Neurology. Reproduced with permission from Wolters Kluwer Health. Unauthorized reproduction of this material is prohibited.
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