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. 2022 Mar 9;22:84. doi: 10.1186/s12883-022-02612-6

Table 1.

Summary of clinical characteristics, investigations, and ‘red flags’ of diagnosis in all three patients

Case 1 Case 2 Case 3 Red flags
Clinical characteristics
   Presenting phenotype Sensory-left arm, tongue Bilateral optic neuritis Optic neuritis

Initial presentation with bilateral optic neuritis and relapse with unilateral optic neuritis is highly suggestive of MOGAD

Relapse with optic neuritis and transverse myelitis also favours MOGAD rather than MS

ADEM phenotype is more common in childhood MOGAD

   Relapse phenotype Unilateral optic neuritis, myelitis, brainstem involvement Unilateral optic neuritis, transverse myelitis Bilateral optic neuritis, transverse myelitis
   Disease course Relapsing Relapsing Relapsing
   Optic neuritis Unilateral (relapse) Bilateral (onset), unilateral (relapse) Bilateral
    ADEM phenotype Yes- on relapse No No
    Myelitis Yes Yes Yes
   Brainstem involvement Yes No No
   Cerebellar involvement No No No
  Response to steroids Recovery from relapse Recovery from relapse Recovery from relapse
  Associated autoimmune diseases Yes No No
MRI brain
  Supratentorial lesions at onset Yes Yes Yes

Dawson’s fingers, U-fibre lesions, and periventricular lesions favour MS

ADEM-type lesions favour MOGAD. Optic nerve involvement is pre-chiasmatic and longitudinally extensive in MOGAD. Perineural and periorbital enhancement favours MOGAD. 15% of MOGAD fulfill McDonald criteria for MS

  ADEM-like lesions (bilateral, asymmetrical) Yes (during relapse) No No
   Brainstem lesions Yes No No
   Dawson’s fingers No Yes Yes
   Subcortical U-fibre lesions No No No
   ≥ 1 lesion adjacent to lateral ventricle Yes Yes Yes
MRI spine
   Length of lesions Short segment, multiple Short segment, multiple Longitudinally extensive, multiple Longitudinally extensive central lesions with grey matter involvement favour MOGAD
   Location of lesions Cervical, thoracic Cervical, thoracic Cervical, thoracic
   Contrast enhancement No No No
CSF
   Pleocytosis Nil Not available Lymphocytes 2X106/L In MOGAD, pleocytosis is variable & intrathecal OCB occur in 5–20% of patients. In MS, OCB present in 95%. Pleocytosis usually absent in MS
   Protein Normal Not available 0.66 g/L (normal 0.15–0.45 g/L)
   Oligoclonal bands (OCB) Negative Not available Positive