Cabrera-Gómez José A, Quevedo-Sotolongo L, González-Quevedo A, Lima S, Real-González Y, Cristófol-Corominas M, Romero-García K, Ugarte-Sánchez C, Jordán-González J, de la Nuez J E González, Lahera J García, Tellez R, Pedroso-Ibañez I, Roca R Rodríguez, Cabrera-Núñez A Y
International Center of Neurological Restoration, Reparto Cubanacán, Playa, Ciudad de La Habana, Cuba.
Mult Scler. 2007 Mar;13(2):186-92. doi: 10.1177/1352458506070725. Epub 2007 Jan 29.
Some studies showed abnormalities in brain magnetic resonance imaging (MRI) of relapsing neuromyelitis optica (R-NMO) from 12 to 46%. These abnormalities are described as compatible/non-compatible with multiple sclerosis (MS).
To describe the abnormal brain MRI lesions in R-NMO with imaging studies conducted with more sensitive white matter change techniques.
Thirty patients with R-NMO were selected. All MRI brain studies were performed with a 1.5-T Siemens MRI system according to the Standardized MR Imaging Protocol for Multiple Sclerosis from the Consortium of MS Centers Consensus Guidelines.
Brain MRI images were evaluated in 29 R-NMO cases because in one case the MRI images were not appropriate for the study. Of these 29 brain MRI studies, 19 cases (65.5%) had at least one or more lesions (1-57) and 10 were negative (34.4%). Brain MRI findings in 19 cases were characterized in T2/fluid-attenuated inversion-recovery (FLAIR) by the presence of subcortical/deep white matter lesions in 16 (84.2%) cases (1-50), most of them <3 mm and without juxtacortical localization. Periventricular lesions were observed in 13 (68.4%) cases, but morphologically they were not oval, ovoid or perpendicularly orientated. Infratentorial lesions, all >3 mm, were observed in 4 (21.05%) cases without cerebellar involvement. T1 studies demonstrated absence of hypointense regions. Optic nerve enhancement was observed in 6/19 patients (31.5%). None of the brain MRI abnormalities observed were compatible with Barkhof et al. criteria of MS.
This study, based on a Cuban patient population, with long duration of disease, good sample size and detailed characterization by MRI, demonstrated the brain MRI pattern of R-NMO patients, which is different from MS.
一些研究显示,复发型视神经脊髓炎(R-NMO)患者脑部磁共振成像(MRI)异常率为12%至46%。这些异常被描述为与多发性硬化症(MS)相符/不相符。
采用更敏感的白质变化技术进行影像学研究,描述R-NMO患者脑部MRI异常病变情况。
选取30例R-NMO患者。所有脑部MRI检查均使用1.5-T西门子MRI系统,按照多发性硬化症中心联盟共识指南的多发性硬化症标准化MR成像方案进行。
对29例R-NMO患者的脑部MRI图像进行了评估,因为有1例患者的MRI图像不适合该研究。在这29例脑部MRI检查中,19例(65.5%)有至少一个或多个病变(1至57个),10例为阴性(34.4%)。19例患者的脑部MRI表现为,在T2/液体衰减反转恢复序列(FLAIR)上,16例(84.2%)出现皮质下/深部白质病变(1至50个),其中大多数病变小于3毫米,且无皮质旁定位。13例(68.4%)出现脑室周围病变,但形态上并非椭圆形、卵圆形或垂直排列。4例(21.05%)出现幕下病变,均大于3毫米,且未累及小脑。T1加权像研究显示无低信号区。19例患者中有6例(31.5%)观察到视神经强化。所观察到的脑部MRI异常均不符合Barkhof等人提出的MS标准。
这项基于古巴患者群体的研究,疾病病程长,样本量充足,且通过MRI进行了详细特征描述,展示了R-NMO患者的脑部MRI模式,该模式与MS不同。