Anti-MDA5 antibody-positive dermatomyositis with mild encephalopathy with reversible splenial lesion: a possible rare association?

被引：2

作者：

Saghir, Khadija ^{[1
,2
,3
]}

Chraa, Mohammed ^{[1
,2
,3
]}

Kissani, Najib ^{[1
,2
,3
]}

Joulal, Hajar ^{[1
,2
,3
]}

Essaadouni, Lamiaa ^{[1
,2
,3
]}

Louhab, Nissrine ^{[1
,2
,3
]}

机构：

[1] Cadi Ayyad Univ, Marrakech Med Sch, Neurosci Res Lab, Marrakech, Morocco

[2] Univ Teaching Hosp Mohammed VI, Dept Neurol, Marrakech, Morocco

[3] Univ Teaching Hosp Mohammed VI, Fac Med, Cadi Ayyad Dept Internal Med, Marrakech, Morocco

来源：

WIENER MEDIZINISCHE WOCHENSCHRIFT | 2023年 / 173卷 / 11-12期

关键词：

Encephalitis; Magnetic resonance imaging; Myopathy; Corpus callosum; Interleukins; ENCEPHALITIS/ENCEPHALOPATHY;

D O I：

10.1007/s10354-022-00943-0

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Central nervous system (CNS) involvement in dermatomyositis (DM) is seldom observed. However, there are very rare case reports of CNS involvement with juvenile dermatomyositis. Encephalopathy in DM may occur for a number of reasons, such as cerebral vasculitis and hypoperfusion/hypertensive encephalopathy, but mostly as a consequence of immunosuppressant treatment. We report here for the first time the case of a patient with two rare diseases, namely anti-MDA5 antibody-positive dermatomyositis and mild encephalopathy with reversible splenial lesion (MERS).

引用

页码：263 / 266

页数：4

共 18 条

[1] Dermatomyositis as a presentation of neuromyelitis optica spectrum disorder [J].