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Frequency of Diencephalic Syndrome in Nmosd Publisher Pubmed



Etemadifar M1 ; Nouri H2 ; Khorvash R2 ; Salari M3 ; Ghafari K4 ; Aghababaee A2
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Authors Affiliations
  1. 1. Department of Neurosurgery, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Alzahra Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Neurological Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. Department of Biological Sciences and Technologies, Isfahan University, Isfahan, Iran

Source: Acta Neurologica Belgica Published:2022


Abstract

Background: Diencephalic region of the brain harbors sites with a considerable amount of aquaporin-4 expression. Neuromyelitis optica spectrum disorder (NMOSD) primarily involves autoimmune processes against this molecule. However, little is known about the frequency of symptoms of diencephalic involvement in NMOSD patients. Objective: To investigate the frequency of symptoms of diencephalic involvement in NMOSD patients and describe the associated characteristics in patients presenting such symptoms. Materials and methods: This retrospective cohort included 145 NMOSD patients (39 males and 106 females) who visited Isfahan Multiple Sclerosis Center from January 2013 to February 2020 for approximately 61 months. Demographic and clinical information of patients and findings from radiological and serological investigations were retrieved. Results: The frequency of diencephalic involvement in NMOSD patients was 3.4% (five cases). Diencephalic syndrome-associated symptoms observed in this cohort consisted of narcolepsy (n = 2; 40%), hypotension (n = 1; 20%), amenorrhea (n = 1; 20%), and syndrome of inappropriate antidiuretic hormone secretion (n = 1; 20%). These manifestations responded well to NMOSD-associated treatments, i.e., rituximab and azathioprine. Conclusion: Although rarely manifested through symptoms suggestive of diencephalic involvement, NMOSD should be considered when encountering patients with the diencephalic syndrome to identify the primary cause of these manifestations. © 2021, Belgian Neurological Society.
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