Pediatric Neuromyelitis Optica Spectrum Disorders: Three Case Reports and Review of Literature

سال انتشار: 1399
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 53

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شناسه ملی سند علمی:

JR_JPRE-8-2_006

تاریخ نمایه سازی: 9 آذر 1402

چکیده مقاله:

Introduction: Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare autoimmune inflammatory and astrocytopathic demyelinating disease of the Central Nervous System (CNS). In most patients, an autoantibody to the water channel protein aquaporin-۴ (AQP۴) would cause humoral inflammatory demyelination and axonal damage. The disease is characterized by clinical syndromes of the optic nerve, area postrema, spinal cord, diencephalon, or cerebrum; or MRI finding related to these regions. According to recent consensus diagnostic criteria, NMOSD is categorized as NMOSD with AQP۴-Ab and NMOSD without AQP۴-Ab. Early onset is defined as the disease presentation before ۱۷ years. According to the pediatric NMOSD working group, most clinical, laboratory characteristics, and neuroimaging findings of this disease are the same as adult onset one, and the same criteria could be used for pediatric NMOSD. Differentiation of Neuromyelitis Optica (NMO) from MS and Acute Disseminated Encephalomyelitis (ADEM) is vital in choosing the appropriate therapy. It has also been reported that some MS therapies could aggravate NMO and lead to permanent disability. Case Presentation: Three patients under the age of ۱۷ years presented in the neurology clinic, because of their recurrent optic neuritis and cervical myelopathy. AQP۴-Ab was positive in two patients, and the other patient was seronegative for AQP۴-Ab. According to the recent international consensus definition, all of the patients went under treatment with corticosteroid pulse therapy in acute relapses. Then two of them received azathioprine as a disease-modifying therapy, and the other patient went under rituximab because of a new relapse in spite of azathioprine therapy. Azathioprine and rituximab were safe, and all patients tolerated them well without any significant side effects. Conclusions: Pediatric NMOSD is a rare but life-threatening disease, which pediatricians and pediatric neurologists must be aware of its presentations and treatment.

کلیدواژه ها:

Pediatric ، Neuromyelitis optica spectrum disorders ، Neuromyelitis optica (NMO)

نویسندگان

Seyed Mohammad Baghbanian

Department of Neurology, Bu-Ali Sina Hospital, Mazandaran University of Medical Sciences, Sari, Iran.

Abdorreza Naser Moghadasi

MS Research Centre, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.

Mohammad Mehdi Nasehi

Pediatric Neurology Research Center, Research Institute for Children Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

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