Ocular flutter as presenting manifestation of pediatric MOG antibody–associated demyelination: A case report

Author:

Breza Marianthi1,Smyrni Nikoletta2,Koutsis Georgios1,Anagnostou Evangelos1,Tzartos John3,Velonakis Georgios4,Kokkinis Constantinos5,Kilindireas Constantinos1,Papavasiliou Antigone2,Kotsalis Charalambos2

Affiliation:

1. 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

2. Neurology Department, Penteli Children’s Hospital, Attica, Greece

3. 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece/Tzartos Neurodiagnostics, Athens, Greece

4. 2nd Department of Radiology, Attikon Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

5. Department of Radiology, General Hospital of Attica, Attica, Greece

Abstract

A 13-year-old girl presented with a 5-day history of oscillopsia. On examination, ocular flutter and mild cerebellar signs were found. Brain magnetic resonance imaging (MRI) revealed four periventricular and subcortical non-enhancing lesions. Cerebrospinal fluid (CSF) oligoclonal bands were negative. Neuroblastoma or other malignancies were not found. She responded well to a corticosteroid–intravenous immunoglobulin (IVIG) combination and remained symptom-free for 3 years until presenting again with isolated ocular flutter. Brain MRI at this time remained atypical for classic multiple sclerosis (MS) with a predominance of juxtacortical demyelinating lesions. CSF was positive for oligoclonal bands. Serum myelin oligodendrocyte glycoprotein (MOG) antibodies were present. Ocular flutter can be the presenting feature of MOG antibody–associated pediatric demyelination.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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