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3D-DIR for early differential diagnostic and prognostic evaluation of NMO
Neuromyelitis optica (NMO) is an acute or subacute lesion of demyelinating disease involving the optic nerve and spinal cord, and imaging techniques and their effects have been the focus of investigations. The aim of the present study was to examine the value of three-dimensional double inversion re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998000/ https://www.ncbi.nlm.nih.gov/pubmed/27588068 http://dx.doi.org/10.3892/etm.2016.3474 |
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author | Wang, Yanbing Yan, Hong Ding, Qixing Mao, Cunhua Shen, Yelong Wang, Guangbin |
author_facet | Wang, Yanbing Yan, Hong Ding, Qixing Mao, Cunhua Shen, Yelong Wang, Guangbin |
author_sort | Wang, Yanbing |
collection | PubMed |
description | Neuromyelitis optica (NMO) is an acute or subacute lesion of demyelinating disease involving the optic nerve and spinal cord, and imaging techniques and their effects have been the focus of investigations. The aim of the present study was to examine the value of three-dimensional double inversion recovery (3D-DIR) in the early differential diagnostic and prognostic evaluation of NMO. Forty-eight patients with suspicious NMO were included into the study and underwent a combination of serum NMO-IgG quantitative detection and 3D-DIR examination. Forty cases (83.3%) of the suspicious cases were confirmed with NMO. The average time from onset to definite diagnosis was 3.5±0.6 days. The brain showed high T2W and fluid-attenuated inversion recovery (FLAIR) signals, involving 5.8±1.2 sites on average, distributed in the peripheral lateral ventricle, medulla, cerebral white matter, the third ventricle, peripheral aqueduct of sylvius, pons and diencephalon. The average T2W signal strength was 2.73±0.12. The signal intensity of DIR was significantly higher than that of T2W and FLAIR, and the difference was statistically significant. The optic nerve and chiasma showed a high FLAIR signal, with an average signal intensity of 2.13±0.14. The spinal cord showed swelling, necrosis and cavity lesion, involving the gray and white matter of the central site, transversely, with an average lesion length of 4.7±0.6 centrum. The relative signal intensity of DIR was significantly higher than that of T2W and FLAIR. Following treatment, the signal intensity of the brain, optic nerve, optic chiasma and spinal cord decreased significantly (P<0.05). In conclusion, 3D-DIR has great application value in the early differential diagnostic and prognostic evaluation of NMO. |
format | Online Article Text |
id | pubmed-4998000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-49980002016-09-01 3D-DIR for early differential diagnostic and prognostic evaluation of NMO Wang, Yanbing Yan, Hong Ding, Qixing Mao, Cunhua Shen, Yelong Wang, Guangbin Exp Ther Med Articles Neuromyelitis optica (NMO) is an acute or subacute lesion of demyelinating disease involving the optic nerve and spinal cord, and imaging techniques and their effects have been the focus of investigations. The aim of the present study was to examine the value of three-dimensional double inversion recovery (3D-DIR) in the early differential diagnostic and prognostic evaluation of NMO. Forty-eight patients with suspicious NMO were included into the study and underwent a combination of serum NMO-IgG quantitative detection and 3D-DIR examination. Forty cases (83.3%) of the suspicious cases were confirmed with NMO. The average time from onset to definite diagnosis was 3.5±0.6 days. The brain showed high T2W and fluid-attenuated inversion recovery (FLAIR) signals, involving 5.8±1.2 sites on average, distributed in the peripheral lateral ventricle, medulla, cerebral white matter, the third ventricle, peripheral aqueduct of sylvius, pons and diencephalon. The average T2W signal strength was 2.73±0.12. The signal intensity of DIR was significantly higher than that of T2W and FLAIR, and the difference was statistically significant. The optic nerve and chiasma showed a high FLAIR signal, with an average signal intensity of 2.13±0.14. The spinal cord showed swelling, necrosis and cavity lesion, involving the gray and white matter of the central site, transversely, with an average lesion length of 4.7±0.6 centrum. The relative signal intensity of DIR was significantly higher than that of T2W and FLAIR. Following treatment, the signal intensity of the brain, optic nerve, optic chiasma and spinal cord decreased significantly (P<0.05). In conclusion, 3D-DIR has great application value in the early differential diagnostic and prognostic evaluation of NMO. D.A. Spandidos 2016-09 2016-06-23 /pmc/articles/PMC4998000/ /pubmed/27588068 http://dx.doi.org/10.3892/etm.2016.3474 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Yanbing Yan, Hong Ding, Qixing Mao, Cunhua Shen, Yelong Wang, Guangbin 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title | 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title_full | 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title_fullStr | 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title_full_unstemmed | 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title_short | 3D-DIR for early differential diagnostic and prognostic evaluation of NMO |
title_sort | 3d-dir for early differential diagnostic and prognostic evaluation of nmo |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998000/ https://www.ncbi.nlm.nih.gov/pubmed/27588068 http://dx.doi.org/10.3892/etm.2016.3474 |
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