A case of bilateral limbic and recurrent unilateral cortical encephalitis with anti-myelin oligodendrocyte glycoprotein antibody positivity

Author(s):  
Takahiro Horita ◽  
Takeshi Inoue ◽  
Ichiro Kuki ◽  
Shizuka Nagase ◽  
Naohiro Yamamoto ◽  
...  
2021 ◽  
Vol 14 (5) ◽  
pp. e240055
Author(s):  
Amlan Kusum Datta ◽  
Adreesh Mukherjee ◽  
Biman Kanti Ray ◽  
Atanu Biswas

A patient having clinical features reminiscent of anterior cord syndrome (ACS) was found to have long segment myelitis on MRI. Investigations revealed serum anti-myelin oligodendrocyte glycoprotein (MOG) antibody positivity. He was treated with pulse methylprednisolone followed by immunosuppressant therapy with mycophenolate mofetil, which led to clinical recovery. Anterior cord syndrome has so far not been reported in the context of anti-MOG antibody associated disease.


Author(s):  
Deirdre O'Sullivan ◽  
Michael Moore ◽  
Susan Byrne ◽  
Andreas O. Reiff ◽  
Susanna Felsenstein

AbstractAcute disseminated encephalomyelitis in association with extensive longitudinal transverse myelitis is reported in a young child with positive anti-myelin oligodendrocyte glycoprotein (MOG) antibody with heterozygous NLRP3 missense mutations; p.(Arg488Lys) and p.(Ser159Ile). This case may well present an exceptional coincidence, but may describe a yet unrecognized feature of the spectrum of childhood onset cryopyrinopathies that contribute to the understanding of the genetic basis for anti-MOG antibody positive encephalomyelitis. Based on this observation, a larger scale study investigating the role of NLRP3 and other inflammasomes in this entity would provide important pathophysiological insights and potentially novel avenues for treatment.


2018 ◽  
Vol 14 (2) ◽  
Author(s):  
Maria-Eleni Androutsou ◽  
Anthi Tapeinou ◽  
Alexios Vlamis-Gardikas ◽  
Theodore Tselios

2021 ◽  
Vol 12 (1) ◽  
pp. 22-41 ◽  
Author(s):  
Sarah Healy ◽  
Kariem Tarik Elhadd ◽  
Emily Gibbons ◽  
Dan Whittam ◽  
Michael Griffiths ◽  
...  

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