Case Report
A Rare Case of Paediatric Myelin Oligodendrocyte Glycoprotein Antibody- Associated Demyelinating Disease Mimicking Typical Multiple Sclerosis
Das A*, Gautam AK, Agarwal S, Kharkwal R, Issar P, Pal R, Gupta DK
Department of Radio diagnosis, JLN Hospital and Research Centre, Sector 9, Bhilai - 490009, Chattisgarh, India
*Corresponding author: Das A, Department of Radio diagnosis, JLN Hospital and Research Centre, Sector 9, Bhilai -
490009, Chattisgarh , India; Mobile: +91 7489740972; E-mail: mukut016@gmail.com
Copyright: © 2022 Das A, et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Article Information: Submission: 27/12/2021; Accepted: 02/02/2022; Published: 05/02/2022
Abstract
Acquired demyelinating disorders of CNS are rare among the pediatric age group, the common ones among them being ADEM, MOGAD, MS and
NMOSD. Clinical history and MRI of the CNS may reveal some soft indicators that help differentiate the demyelinating disorders, which are extremely
important from the perspective of treatment and prognosis. However, a few overlapping clinical and imaging features may be seen among these disorders.
We present a case of pediatric MOGAD, which had initially mimicked pediatric MS clinically and imaging-wise. We also present his clinico-radiological followup
over a period of 6 years.