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Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage

The patient was a woman without hypertension who had previously experienced intracranial hemorrhage twice at 48 and 56 years of age. At 59 years of age, she was diagnosed with neuromyelitis optica spectrum disorder (NMOSD) based on the presence of a brain stem lesion and the detection of anti-aquapo...

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Autores principales: Yaguchi, Hiroaki, Mito, Yasunori, Ohashi, Ikkei, Nomura, Taichi, Yabe, Ichiro, Tajima, Yasutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519480/
https://www.ncbi.nlm.nih.gov/pubmed/28674367
http://dx.doi.org/10.2169/internalmedicine.56.7889
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author Yaguchi, Hiroaki
Mito, Yasunori
Ohashi, Ikkei
Nomura, Taichi
Yabe, Ichiro
Tajima, Yasutaka
author_facet Yaguchi, Hiroaki
Mito, Yasunori
Ohashi, Ikkei
Nomura, Taichi
Yabe, Ichiro
Tajima, Yasutaka
author_sort Yaguchi, Hiroaki
collection PubMed
description The patient was a woman without hypertension who had previously experienced intracranial hemorrhage twice at 48 and 56 years of age. At 59 years of age, she was diagnosed with neuromyelitis optica spectrum disorder (NMOSD) based on the presence of a brain stem lesion and the detection of anti-aquaporin 4 (AQP4) antibodies. After 5 months of continuous treatment with prednisolone (15 mg/day), she presented with optic neuritis and intracranial bleeding. A recurrent attack of NMOSD and intracranial hemorrhage were concurrently diagnosed. We herein report a case of NMOSD with recurrent intracranial hemorrhage, which indicates an association between NMOSD and cerebellar vascular dysfunction.
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spelling pubmed-55194802017-07-27 Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage Yaguchi, Hiroaki Mito, Yasunori Ohashi, Ikkei Nomura, Taichi Yabe, Ichiro Tajima, Yasutaka Intern Med Case Report The patient was a woman without hypertension who had previously experienced intracranial hemorrhage twice at 48 and 56 years of age. At 59 years of age, she was diagnosed with neuromyelitis optica spectrum disorder (NMOSD) based on the presence of a brain stem lesion and the detection of anti-aquaporin 4 (AQP4) antibodies. After 5 months of continuous treatment with prednisolone (15 mg/day), she presented with optic neuritis and intracranial bleeding. A recurrent attack of NMOSD and intracranial hemorrhage were concurrently diagnosed. We herein report a case of NMOSD with recurrent intracranial hemorrhage, which indicates an association between NMOSD and cerebellar vascular dysfunction. The Japanese Society of Internal Medicine 2017-07-01 /pmc/articles/PMC5519480/ /pubmed/28674367 http://dx.doi.org/10.2169/internalmedicine.56.7889 Text en Copyright © 2017 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yaguchi, Hiroaki
Mito, Yasunori
Ohashi, Ikkei
Nomura, Taichi
Yabe, Ichiro
Tajima, Yasutaka
Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title_full Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title_fullStr Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title_full_unstemmed Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title_short Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage
title_sort neuromyelitis optica spectrum disorder with recurrent intracranial hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519480/
https://www.ncbi.nlm.nih.gov/pubmed/28674367
http://dx.doi.org/10.2169/internalmedicine.56.7889
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