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

被引:11
作者
Breza, Marianthi [1 ]
Smyrni, Nikoletta [2 ]
Koutsis, Georgios [1 ]
Anagnostou, Evangelos [1 ]
Tzartos, John [1 ,3 ]
Velonakis, Georgios [4 ]
Kokkinis, Constantinos [5 ]
Kilindireas, Constantinos [1 ]
Papavasiliou, Antigone [2 ]
Kotsalis, Charalambos [2 ]
机构
[1] Univ Athens, Med Sch, Eginit Hosp, Dept Neurol 1, 72-74 Vasilissis Sofias, GR-11528 Athens, Greece
[2] Penteli Childrens Hosp, Neurol Dept, Attica, Greece
[3] Tzartos Neurodiagnost, Athens, Greece
[4] Univ Athens, Attikon Hosp, Med Sch, Dept Radiol 2, Athens, Greece
[5] Gen Hosp Attica, Dept Radiol, Attica, Greece
关键词
Ocular flutter; MOG antibodies; multiple sclerosis; oscillopsia; MOG antibody-associated demyelination; pediatric MS; CLINICAL-COURSE; RESPONSES; CHILDREN;
D O I
10.1177/1352458518771872
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:122 / 125
页数:4
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