Departamento de Neurologia, Universidade Federal do Estado do Rio de Janeiro, Rua Mariz e Barros 775, Tijuca, Rio de Janeiro 20270-004, Brazil.
J Neurol. 2010 Jun;257(6):992-8. doi: 10.1007/s00415-009-5450-6. Epub 2010 Feb 3.
The aim of this study was to describe the demographic, clinical and laboratory features of idiopathic acute transverse myelitis (IATM). Patients with non-compressive ATM receiving care at Hospital da Lagoa, Rio de Janeiro (Brazil) between 2000 and 2008 were selected. Of the 70 cases of acute myelopathies, the idiopathic form was identified in 41 following exclusion of the cases associated with systemic lupus erythematosus (n = 1), Sjogren's syndrome (n = 1), herpes zoster (n = 1), cytomegalovirus in an HIV-positive patient (n = 1), Schistosoma mansoni (n = 1), actinic myelitis (n = 1), infectious myelitis of unknown etiology (n = 2) and those that, following the first attack of myelitis, converted to NMO (n = 19) or to clinically defined MS (n = 2). Of the 41 cases of IATM, the majority of patients were female (68.3%) and white (65.9%). Median age at first myelitis was 37.0 +/- 11.8 years. Over a median observation time of 36 months, 39.0% of patients remained monophasic, while recurrences occurred in 61.0% of cases. The number of ATM/patient ranged from one to seven. Among the recurrent cases the median time between the first and the second ATM was 12 months (range 1-150 months).The first myelitis was characterized mainly by partial myelitis with motor and sensorial dysfunction (63.4%). Complete and severe myelitis occurred more frequently among monophasic patients and partial myelitis with moderate dysfunction at onset in recurrent cases; however, over the long-term, dysfunction and disability were mild in both groups. Serial spine MRI confirmed spinal cord inflammation in 92.0% of cases and extensive spinal cord lesion was identified in 61.0%. Brain MRI was normal or not suggestive of MS in 94.4% of cases. CSF showed pleocytosis in 41.2%, increased IgG index in 24.0% and oligoclonal bands in 38.0% of 34 patients tested. Abnormal visual evoked potentials occurred in 11.5% of 26 patients. Positivity for anti-AQP4 was found in 23.5% of the 17 cases tested, suggesting limited forms of NMO. This study suggests some new aspects of the clinical course of IATM such as the high conversion rate to NMO, the predominance of women and a higher frequency of recurrent forms.
本研究旨在描述特发性急性横贯性脊髓炎(IATM)的人口统计学、临床和实验室特征。选择了 2000 年至 2008 年在里约热内卢拉戈阿医院(巴西)接受治疗的非压迫性 ATM 患者。在 70 例急性脊髓病中,排除与系统性红斑狼疮(n=1)、干燥综合征(n=1)、带状疱疹(n=1)、HIV 阳性患者的巨细胞病毒(n=1)、曼氏血吸虫(n=1)、光化性脊髓炎(n=1)、病因不明的传染性脊髓炎(n=2)以及在首次脊髓炎发作后转化为 NMO(n=19)或临床定义的 MS(n=2)的病例后,发现特发性病例为 41 例。在这 41 例 IATM 患者中,大多数患者为女性(68.3%)和白人(65.9%)。首次发生脊髓炎时的中位年龄为 37.0+/-11.8 岁。在中位观察时间 36 个月内,39.0%的患者为单相病程,而 61.0%的患者出现复发。每位患者的 ATM 发作次数为 1-7 次。在复发病例中,首次和第二次 ATM 之间的中位时间为 12 个月(1-150 个月)。首次脊髓炎的特征主要为部分性脊髓炎,伴有运动和感觉功能障碍(63.4%)。单相患者更常出现完全性和严重脊髓炎,而复发性病例首发时为部分性脊髓炎伴中度功能障碍;然而,在长期随访中,两组的功能和残疾均较轻。连续脊柱 MRI 证实 92.0%的病例存在脊髓炎症,61.0%的病例存在广泛的脊髓病变。94.4%的病例脑部 MRI 正常或不提示 MS。34 例接受检测的患者中,41.2%的脑脊液出现细胞增多,24.0%的 IgG 指数升高,38.0%的寡克隆带阳性。26 例接受检测的患者中有 11.5%的视觉诱发电位异常。17 例接受检测的患者中有 23.5%的抗 AQP4 阳性,提示存在局限性 NMO。本研究提示了 IATM 临床病程的一些新特征,如向 NMO 的高转化率、女性为主和复发性疾病的高频率。