Neuromyelitis optica spectrum disorder

Neuromyelis optica (NMO) and neuromyelitis optica spectrum disorder (NMOSD) are closely related severe demyelinating diseases caused by an autoantibody to the aquaporin-4 water channel. The classic presentation of NMO is with the triad of optic neuritislongitudinally extensive myelitis, and positive anti-AQP4 antibody, although a far wider range of manifestations are now recognized as part of NMOSD 8-13.

Neuromyelitis optica (NMO) was previously referred to as Devic disease, and traditionally NMO was thought to have limited if any intracranial manifestations. Over the past decade, however, a far wider range of manifestations have been recognized as belonging together and thus the term NMOSD has been proposed to encompass them all. 

Neuromyelitis optica is typically found in patients somewhat older than those with multiple sclerosis (MS), with an average of presentation of 41 years, and there is an even stronger female predilection (F:M  6.5:1) 6,8. It is found more frequently in patients of Asian, Indian, and African descent 8

NMO is characterized by bilateral optic neuritis and myelitis resulting in blindness and paraplegia. Although the two usually present concurrently, it is not uncommon for one to precede the other by up to several weeks 3. Additionally, it is now recognized that some patients present with unilateral optic nerve involvement. 

Although NMO was initially thought of as a monophasic illness, it is now evident that, as with MS, it is usually a relapsing-remitting disease with symptomatic events separated by many years 5

Furthermore, NMOSD also encompasses non-neurological manifestations in anti-AQP4 antibody seropositive patients including systemic lupus erythematosus (SLE) and Sjögren syndrome 13.

The current diagnostic criteria are defined by the International Panel for NMO Diagnosis.

In approximately 70% (sensitivity of 70-90%; specificity of 90%) of patients with established NMO, a specific immunoglobulin can be isolated (AQP4-IgG which targets a transmembrane water channel (aquaporin 4) present on astrocyte foot processes abutting the limiting membrane 5,8. This accounts for some of the predilection for the circumventricular organs (e.g. periaqueductal grey matter) which are particularly rich in aquaporin 4 8

Early in the disease, demyelinating regions will demonstrate similar findings to MS, such as macrophage/microglia activation and axonal damage. Additionally, however, and relatively specific for NMO, these regions will also demonstrate extensive eosinophilic infiltration, perivascular deposition of immunoglobulins (especially IgM) and local activation of the complement cascade 3. Another differentiating feature is that axonal damage precedes demyelination in NMO 5

Generally, the condition is sporadic, although some overlap in immunogenic features between certain viruses and aquaporin-4 water channel have been identified 8

A significant proportion of individuals presenting with NMO but without AQP4 antibodies will be found to have anti-MOG IgG antibodies 16. These individuals appear to have somewhat different demographics and less severe clinical course 16

MRI is the modality of choice for NMOSD and the orbits, brain and spinal cord should be imaged in suspected cases. 

Targeted imaging of the orbits (including fat saturated T1 C+ and T2 weighted sequences (see MRI protocol: orbit) may demonstrate typical features of optic neuritis

  • optic nerves appearing hyperintense and swollen on T2 weighted sequences and enhancing on T1 C+
  • bilateral optic nerve involvement and extension of the abnormal signal posteriorly as far as the chiasm is particularly suggestive of NMO 5
  • atrophy of the optic nerves with associated hyperintensities on T2 weighted sequences may be seen in chronic stages of the disease 11

Although traditionally NMO was thought to have normal intracranial appearance it is increasingly evident that asymptomatic abnormalities are present in the majority of seropositive NMOSD patients. These can be divided into four categories 5,8,13:

  1. lesions which mirror the distribution of aquaporin 4 in the brain, which is particularly found in the periependymal regions abutting the ventricles:
    • periventricular (hemispheric) confluent smooth sessile white matter involvement (unlike MS, there are usually no Dawson's fingers)
    • periaqueductal grey matter
    • hypothalamus/medial thalamus
    • dorsal pons/medulla 
    • corpus callosum
      • multiple callosal lesions with heterogeneous signal leading to a marbled pattern 7 
      • the splenium may be diffusely involved and expanded
  2. deep (or less frequently subcortical) punctate white matter lesions (which may appear similar to those seen in MS)
  3. corticospinal tract involvement by extensive longitudinal lesions; has been reported more frequently in Korean patients 5
  4. larger >3 cm diameter hemispheric white matter lesions
    • radially oriented (spilled-ink appearances) or spindle-shaped
    • limited if any mass effect although tumefactive lesions do occur 13
    • may involve overlying cortex 14
    • facilitated diffusion
    • may be more common in children and in patients from the Far East and Africa
    • often vanish but cystic change is seen in a minority of cases 13

Spinal cord involvement is extensive, with high T2 signal spanning at least three vertebral segments, often many more (known as a longitudinally extensive spinal cord lesion4,5,8,11. Cord swelling is usually present in the acute phase. Although less common, short transverse myelitis is seen in 14.5% of cases 11.

Bright spotty lesions are a specific feature of NMO. It consists of marked T2 hyperintense (higher than CSF) and T1 hypointense foci in the central grey matter.

Imaging features include 5,8

  • T1
    • hypointense
    • follow-up scans may demonstrate cord atrophy and low T1 signal 5
  • T2
    • hyperintense (often >3 vertebral body lengths) 
    • central grey matter involvement
    • bright spotty lesions (see above)
  • T1 C+ (Gd)
    • enhancement is common and variable in appearance
    • ring-enhancement
      • seen in a third of patients 17
      • both on sagittal and axial imaging
      • often ring extends over multiple vertebral levels 
    • patchy "cloud-like" enhancement of the aforementioned T2 bright lesions may be present
    • thin ependymal enhancement similar to ependymitis
    • lens-shaped enhancement on sagittal images 11

Treatment of NMO is evolving, with immunosuppression (e.g. anti-CD20 monoclonal antibody rituximab) appearing effective 5.

It is important to distinguish NMO from MS as the treatment not only is different but treating a patient with NMO with MS-specific therapies (e.g. beta-interferon or natalizumab) can actually lead to its exacerbation 5

Patients with a relapsing course have a poorer prognosis 4:

  • blind in one or both eyes: monophasic  22% vs. relapsing 60%
  • monoplegia or paraplegia: monophasic 31% vs. relapsing 52%

The disease was first described in 1870 by Sir Thomas Clifford Allbutt 12. The French term "neuromyélite optique aiguë" (literally acute optic neuromyelitis) was later coined by Dr Eugène Devic and Fernand Gault in 1894 in a case series of 16 patients 12. At the time, the disorder was thought to be acute and monophasic.

For many years, it was considered to be a subtype of multiple sclerosis, until the discovery of anti aquaporin-4 antibodies at which time it was moved into its own disease category. It is now evident that a significant proportion of patients with clinical NMO do not have the anti-AQP4-antibody (some have anti-MOG-antibodies for example) and that the presentation can be more heterogeneous. At present, therefore, the term neuromyelitis optica spectrum disorder (NMOSD) is now used. It is very likely that there will be significant further evolution of our understanding of this disease in the near future. 

The differential diagnosis depends on the presentation, and when classic, the diagnosis can be made with a fair degree of certainty. The most important clinical and imaging differential is MS as both can present with optic neuritis, cerebral and spinal demyelination including involvement of the corpus callosum (see Practical points).

For patients with cerebral involvement, the differential is broad and includes:

For patients with optic nerve involvement, the differential is that of optic neuritis.

For patients with spinal cord involvement, the differential is that of a longitudinally extensive spinal cord lesion. For the typical bright spotty lesion, an important differential is acute spinal cord ischemia.

There are many features that distinguish NMO from multiple sclerosis, although none are pathognomonic. It should also be noted that overlap of imaging findings of these two entities may be higher in Asian populations 15. Nonetheless, features that are helpful in favoring NMO over multiple sclerosis include 5,7,15

  • brain
    • smooth confluent periependymal distribution (see above)
    • fewer oval perivenular orientation of periventricular lesions (no Dawson's fingers)
    • fewer juxtacortic lesions (U-fiber)
    • more extensive involvement of the corpus callosum (especially its ependymal surface)
    • larger, more confluent lesions
    • lack of open ring enhancement
    • corticospinal tract and diencephalic involvement (see above)
  • spinal cord
    • more longitudinally extensive spinal cord lesion
      • preferential involvement of the central cord rather than the peripheral cord
  • optic nerves
    • more longitudinally extensive optic neuritis
      • with preferential involvement of the posterior optic pathway 
White matter disorders
Share article

Article information

rID: 1218
Synonyms or Alternate Spellings:
  • Neuromyelitis optica (NMO)
  • NMO
  • Devic neuromyelitis optica
  • Devic's neuromyelitis optica
  • Devic syndrome
  • NMO spectrum disorder
  • Devic disease
  • Devic's disease
  • NMOSD
  • NMOSD

Support Radiopaedia and see fewer ads

Cases and figures

  • Fig 1: NMO distribution
    Drag here to reorder.
  • Case 1
    Drag here to reorder.
  • Case 2
    Drag here to reorder.
  • Case 3: bright spotty lesion
    Drag here to reorder.
  • Axial Flair image...
    Case 4: periaqueductal hyperintensities
    Drag here to reorder.
  • Updating… Please wait.

     Unable to process the form. Check for errors and try again.

     Thank you for updating your details.