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Central nervous system (CNS) inflammatory demyelinating diseases (IDDs) associated with COVID-19: A case series and review.
Feizi, Parissa; Sharma, Kanika; Pasham, Shreya R; Nirwan, Lalit; Joseph, Joe; Jaiswal, Shruti; Sriwastava, Shitiz.
Afiliación
  • Feizi P; Department of Neuroradiology, West Virginia University, Morgantown, WV, USA.
  • Sharma K; Department of Neurology, West Virginia University, Morgantown, WV, USA.
  • Pasham SR; Malla Reddy Institute of Medical Sciences (MRIMS), Hyderabad, India.
  • Nirwan L; Meditrina Institute of Medical Sciences, Nagpur, India.
  • Joseph J; Department of Neuroradiology, West Virginia University, Morgantown, WV, USA.
  • Jaiswal S; West Virginia Clinical Translational Science, Morgantown, WV, USA.
  • Sriwastava S; Department of Neurology, West Virginia University, Morgantown, WV, USA; West Virginia Clinical Translational Science, Morgantown, WV, USA. Electronic address: shitiz.sriwastava@hsc.wvu.edu.
J Neuroimmunol ; 371: 577939, 2022 10 15.
Article en En | MEDLINE | ID: mdl-35939945
ABSTRACT

BACKGROUND:

Over the past two years, SARS-CoV-2 has frequently been documented with various post and para-infectious complications, including cerebrovascular, neuromuscular, and some demyelinating conditions such as acute disseminated encephalomyelitis (ADEM). We report two rare neurological manifestations post-COVID-19 infection; multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Further, we reviewed other CNS inflammatory demyelinating diseases (IDDs) associated with SARS-CoV-2, including optic neuritis (ON) and neuromyelitis optica spectrum disorders (NMOSD).

METHODS:

A descriptive analysis and literature search of Google Scholar and PubMed was conducted by two independent reviewers from December 1st, 2019, to March 30th, 2022, and included all the case studies of MS, MOGAD, NMOSD, and ON associated with COVID-19 infection. CASE PRESENTATIONS Case 1 (MS) was a 24-year-old female with paresthesia and bilateral weakness one week after COVID-19 symptom onset who showed demyelinating plaques and 12 isolated oligoclonal bands (OCBs). Case 2 (MOGAD) was a 41-year-old male with encephalomyelitis 16 days after COVID-19, who later developed MOG-antibody-associated optic neuritis.

RESULTS:

Out of 18 cases, NMOSD was the most common post-COVID manifestation (7, 39%), followed by MOGAD (5, 28%), MS (4, 22%), and isolated ON (2, 11%). The median duration between the onset of COVID-19 symptom onset and neurological symptoms was 14 days. 61% of these were male, with a mean age of 35 years. IVMP was the treatment of choice, and nearly all patients made a full recovery, with zero fatalities.

CONCLUSIONS:

Although these neurological sequelae are few, physicians must be cognizant of their underlying pathophysiology and associated clinical and neuro-diagnostic findings when treating COVID-19 patients with atypical presentations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Central / Neuritis Óptica / Neuromielitis Óptica / COVID-19 / Esclerosis Múltiple Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Neuroimmunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Central / Neuritis Óptica / Neuromielitis Óptica / COVID-19 / Esclerosis Múltiple Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Neuroimmunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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