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Two cases of myelin oligodendrocyte glycoprotein antibody-associated disease presenting with Cauda Equina Syndrome without conus myelitis

Authors
Kang, MS[Kang, Min sung]Kim, MK[Kim, Min Kyoung]Kim, YE[Kim, Ye eun]Kim, JH[Kim, Ji Hyun]Kim, BJ[Kim, Byoung Joon]Lee, HL[Lee, Hye Lim]
Issue Date
Jul-2021
Publisher
ELSEVIER SCI LTD
Keywords
Cauda equina syndrome; Lumbosacral radiculomyelitis; Myelin oligodendrocyte glycoprotein antibody-associated disease; MOGAD; MOG antibody
Citation
MULTIPLE SCLEROSIS AND RELATED DISORDERS, v.52
Indexed
SCIE
SCOPUS
Journal Title
MULTIPLE SCLEROSIS AND RELATED DISORDERS
Volume
52
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/17211
DOI
10.1016/j.msard.2021.103017
ISSN
2211-0348
Abstract
Myelin oligodendrocyte glycoprotein antibody-associated disorder (MOGAD) is a central nervous system inflammatory disorder associated with MOG antibodies. Two patients with clinical symptoms of cauda equina syndrome had positive serum MOG antibody tests, and spinal magnetic resonance imaging showed cauda equina enhancement. They were diagnosed with incomplete cauda equina syndrome associated with MOGAD. A few cases of lumbosacral radiculomyelitis associated with MOGAD have been reported; however, this is the first report of isolated lumbosacral radiculitis associated with MOGAD without transverse myelitis. The MOG antibody test should be considered for cauda equina syndrome without compressive lesions.
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