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MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein.

Authors :
Baumann M
Grams A
Djurdjevic T
Wendel EM
Lechner C
Behring B
Blaschek A
Diepold K
Eisenkölbl A
Fluss J
Karenfort M
Koch J
Konuşkan B
Leiz S
Merkenschlager A
Pohl D
Schimmel M
Thiels C
Kornek B
Schanda K
Reindl M
Rostásy K
Source :
Journal of neurology [J Neurol] 2018 Apr; Vol. 265 (4), pp. 845-855. Date of Electronic Publication: 2018 Feb 08.
Publication Year :
2018

Abstract

Antibodies against the myelin oligodendrocyte glycoprotein (MOG-Ab) can be detected in various pediatric acquired demyelinating syndromes (ADS). Here, we analyze the spectrum of neuroradiologic findings in children with MOG-Ab and a first demyelinating event. The cerebral and spinal MRI of 69 children with different ADS was assessed in regard to the distribution and characteristics of lesions. Children with acute disseminated encephalomyelitis (n = 36) or neuromyelitis optica spectrum disorder (n = 5) presented an imaging pattern characterized predominantly by poorly demarcated lesions with a wide supra- and infratentorial distribution. Younger children also tended to have poorly defined and widespread lesions. The majority of patients with an isolated optic neuritis (n = 16) only presented small non-specific brain lesions or none at all. A longitudinally extensive transverse myelitis mainly affecting the cervical, and less often so the thoracic, lumbar, and conus regions, was detected in 31 children. The three children of our cohort who were then finally diagnosed with multiple sclerosis had at onset already demarcated white matter lesions as well as transverse myelitis. In conclusion, children with MOG seropositive ADS present disparate, yet characteristic imaging patterns. These patterns have been seen to correlate to the disease entity as well as to age of symptom onset.

Details

Language :
English
ISSN :
1432-1459
Volume :
265
Issue :
4
Database :
MEDLINE
Journal :
Journal of neurology
Publication Type :
Academic Journal
Accession number :
29423614
Full Text :
https://doi.org/10.1007/s00415-018-8781-3