Pseudotumoural optic neuritis in myelin oligodendrocyte glycoprotein antibody-associated disease in children Pseudotumoural optic neuritis in MOG antibody-associated disease

被引：0

作者：

Roux, Julia ^{[1
]}

Bommier-Laur, Domitille ^{[4
]}

Calota, Mariana ^{[3
]}

Auvin, Stephane ^{[4
]}

Deiva, Kumaran ^{[1
,2
]}

机构：

[1] Bicetre Hosp, AP HP, Dept Pediat Neurol, 78 Rue Gen ?Leclerc, Le Kremlin Bicetre, France

[2] Paris Sud Saclay Univ, Le Kremlin Bicetre, France

[3] Bicetre Hosp, AP HP, Dept Paediat Radiol, Le Kremlin Bicetre, France

[4] Robert Debre Hosp, AP HP, Dept Pediat Neurol, Paris, France

来源：

ARCHIVES DE PEDIATRIE | 2025年 / 32卷 / 02期

关键词：

Children; MOGAD; Pseudotumoural; Optic neuritis; NMOSD;

D O I：

10.1016/j.arcped.2024.11.005

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is a neuro-inflammatory condition affecting adults and children. The presentations vary and include acute disseminated encephalomyelitis, optic neuritis or transverse myelitis. Optic neuritis associated with anti-MOG antibodies is typically bilateral, anterior and initially severe but usually resolves quickly and completely. Here, we describe 3 children with pseudotumoural optic neuritis associated with anti-MOG antibodies and their outcome. Recognizing these unusual presentations may reduce unnecessary work-ups and improve functional prognosis by implementing rapid and adequate treatment.

引用

页码：143 / 146

页数：4

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