دوره 5، شماره 2 - ( 2-1398 )                   جلد 5 شماره 2 صفحات 96-100 | برگشت به فهرست نسخه ها


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Manouchehri N, Nehzat N, Mirmosayeb O, Shaygannejad V, Barzegar M. Tumefactive Brain Lesions in Patients with Neuromyelitis Optica Spectrum Disorder. Caspian.J.Neurol.Sci. 2019; 5 (2) :96-100
URL: http://cjns.gums.ac.ir/article-1-257-fa.html
Tumefactive Brain Lesions in Patients with Neuromyelitis Optica Spectrum Disorder. مجله علوم اعصاب کاسپین. 1398; 5 (2) :96-100

URL: http://cjns.gums.ac.ir/article-1-257-fa.html


چکیده:   (360 مشاهده)
Background: Neuromyelitis Optica Spectrum Disorder (NMOSD) is an autoimmune neurological disorder that is characterized by optic neuritis and longitudinally-extended transverse myelitis lesions in spinal segments. Magnetic Resonance Imaging (MRI) findings are part of the diagnostic process in NMOSD patients, and abnormal lesion patterns may cause deviation from a correct diagnosis. 
Clinical Presentation and Intervention: A 43-year-old female patient with abrupt cognitive loss, motor dysfunction and tumefactive spread of the demyelinating lesions in her brain presented to the Neurology Clinic of Kashani Hospital. Anti Aquaporine 4(AQP-4) antibody was observed, and the patient responded well to the NMOSD treatment. 
Conclusion: NMOSD can be considered a differential diagnosis during an episode of Fulminant Demyelinating Disorder (FDD) with the tumefactive spread of the lesions.
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نوع مطالعه: گزارش مورد | موضوع مقاله: تخصصي
دریافت: ۱۳۹۷/۱۰/۲۹ | پذیرش: ۱۳۹۷/۱۲/۸ | انتشار: ۱۳۹۸/۱/۱۲

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