Brain abnormalities in neuromyelitis optica

被引:44
作者
Kim, Jee-Eun [1 ]
Kim, Sung-Min [2 ]
Ahn, Suk-Won [3 ]
Lim, Bung Chan [4 ]
Chae, Jong Hee [4 ]
Hong, Yoon-Ho [5 ]
Park, Kyung-Seok [2 ]
Sung, Jung-Joon [1 ]
Lee, Kwang-Woo [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Dept Neurol, Seoul 110744, South Korea
[2] Seoul Natl Univ, Bundang Hosp, Dept Neurol, Kyeunggido, South Korea
[3] Chung Ang Univ, Coll Med, Chung Ang Univ Hosp, Dept Neurol, Seoul 156756, South Korea
[4] Seoul Natl Univ, Coll Med, Seoul Natl Univ Childrens Hosp, Dept Pediat, Seoul 110744, South Korea
[5] Seoul Boramae Hosp, Dept Neurol, Seoul, South Korea
关键词
Neuromyelitis optics; Devic disease; Multiple sclerosis; Brain magnetic resonance imaging; Aquaporin-4; antibody; Asians; Koreans; FRENCH-WEST-INDIES; MULTIPLE-SCLEROSIS; ANTI-AQUAPORIN-4; ANTIBODY; TRANSVERSE MYELITIS; MRI; DISORDERS; SPECTRUM; CRITERIA; ONSET; JAPAN;
D O I
10.1016/j.jns.2010.12.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Differentiating neuromyelitis optica (NMO) from multiple sclerosis (MS) is a real challenge in the clinical field. In the past, NMO (not MS), was inferred when abnormality was not detected in the brain magnetic resonance imaging (MRI). Recently, some studies have reported abnormalities in the brain MRIs of NMO, but only few among the Asian population. The aim of this study was to evaluate the frequency of brain MRI among Korean NMO patients and characterize findings that might be helpful to distinguish NMO from MS. Methods: Medical records, NMO-IgG, and brain MRI of 17 patients diagnosed with NMO by the revised diagnostic criteria of Wingerchuk et al. (2006) [6] from 2008 to 2010, were reviewed. Results: 11 out of 17 patients (64.7%) had abnormal MRI findings. More than two lesions were detected in most patients. The majority of patients with brain MRI abnormality showed nonspecific (5 patients) or atypical (6 patients) findings. Cerebral white matter was most frequently involved (58.8%). 3 patients (17.6%) involved corpus callosum, 4(23.5%) with intemal capsule, 2 (11.8%) with cerebellum, and 3 (17.6%) with brainstem. There were 5 (29.4%) patients who met the Paty et al. criteria (1988) [15] and 3 patients (35.3%) who met the multiple sclerosis (MS) spatial distribution diagnostic criteria of Barkhof et al. (1997) [14] in their brain MRI. Conclusions: Brain abnormalities have been frequently found among Korean NMO patients and the frequencies have been reported to be higher than that of Caucasians. Current MS spatial distribution criteria, such as Paty et al. (1988) [15] or Barkhof et al. (1997) [14], are not sufficient to discriminate NMO from MS in brain MRI findings. Our results will provide valuable information that would be useful in establishing future revising criteria for NMO. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 48
页数:6
相关论文
共 42 条
[1]  
AKMANDEMIR G, 2010, J NEUROL 1017
[2]   Long-term MRI observations of childhood-onset relapsing-remitting multiple sclerosis [J].
Balássy, C ;
Bernert, G ;
Wöber-Bingöl, C ;
Csapó, B ;
Kornek, B ;
Széles, J ;
Fleischmann, D ;
Prayer, D .
NEUROPEDIATRICS, 2001, 32 (01) :28-37
[3]   Neuromyelitis optica-IgG in childhood inflammatory demyelinating CNS disorders [J].
Banwell, B. ;
Tenembaum, S. ;
Lennon, V. A. ;
Ursell, E. ;
Kennedy, J. ;
Bar-Or, A. ;
Weinshenker, B. G. ;
Lucchinetti, C. F. ;
Pittock, S. J. .
NEUROLOGY, 2008, 70 (05) :344-352
[4]   Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis [J].
Barkhof, F ;
Filippi, M ;
Miller, DH ;
Scheltens, P ;
Campi, A ;
Polman, CH ;
Comi, G ;
Ader, HJ ;
Losseff, N ;
Valk, J .
BRAIN, 1997, 120 :2059-2069
[5]   Devic's neuromyelitis optica: clinical features and prognostic factors [J].
Bergamaschi, R ;
Ghezzi, A .
NEUROLOGICAL SCIENCES, 2004, 25 (Suppl 4) :S364-S367
[6]   Neuromyelitis optica in a mother and daughter [J].
Braley, Tiffany ;
Mikol, Daniel D. .
ARCHIVES OF NEUROLOGY, 2007, 64 (08) :1189-1192
[7]   MS and neuromyelitis optics in Martinique (French West Indies) [J].
Cabre, P ;
Heinzlef, O ;
Merle, H ;
Buisson, GG ;
Bera, O ;
Bellance, R ;
Vernant, JC ;
Smadja, D .
NEUROLOGY, 2001, 56 (04) :507-514
[8]   Neuromyelitis optica positive antibodies confer a worse course in relapsing-neuromyelitis optica in Cuba and French West Indies [J].
Cabrera-Gomez, J. A. ;
Bonnan, M. ;
Gonzalez-Quevedo, A. ;
Saiz-Hinarejos, A. ;
Marignier, R. ;
Olindo, S. ;
Graus, F. ;
Smadja, D. ;
Merle, H. ;
Thomas, L. ;
Gomez-Garcia, A. ;
Cabre, P. .
MULTIPLE SCLEROSIS JOURNAL, 2009, 15 (07) :828-833
[9]   Brain magnetic resonance imaging findings in relapsing neuromyelitis optica [J].
Cabrera-Gomez, Jose A. ;
Quevedo-Sotolongo, L. ;
Gonzalez-Quevedo, A. ;
Lima, S. ;
Real-Gonzalez, Y. ;
Cristofol-Corominas, M. ;
Romero-Garcia, K. ;
Ugarte-Sanchez, C. ;
Jordan-Gonzalez, J. ;
Gonzalez de la Nuez, J. E. ;
Garcia Lahera, J. ;
Tellez, R. ;
Pedroso-Ibanez, I. ;
Rodriguez Roca, R. ;
Cabrera-Nunez, A. Y. .
MULTIPLE SCLEROSIS, 2007, 13 (02) :186-192
[10]   Aquaporin-4 autoantibodies in neuromyelitis optica spectrum disorders: comparison between tissue-based and cell-based indirect immunofluorescence assays [J].
Chan, Koon H. ;
Kwan, Jason S. C. ;
Ho, Philip W. L. ;
Ho, Jessica W. M. ;
Chu, Andrew C. Y. ;
Ramsden, David B. .
JOURNAL OF NEUROINFLAMMATION, 2010, 7