Ford B, Tampieri D, Francis G
Department of Neurology, McGill University Faculty of Medicine, Montreal, PQ, Canada.
Neurology. 1992 Jan;42(1):250-2. doi: 10.1212/wnl.42.1.250.
We carried out a prospective, long-term, combined clinical and MRI follow-up study on 15 patients hospitalized at the Montreal Neurological Institute between 1985 and 1988 with a diagnosis of acute partial transverse myelopathy of unknown etiology. Twelve of the 15 (80%) developed clinically definite or lab-supported definite multiple sclerosis (MS) by the end of a mean follow-up period of 38.5 months. The presence of CNS periventricular white matter lesions by cranial MRI at onset increased the likelihood of development of MS to 93%.
我们对1985年至1988年间在蒙特利尔神经病学研究所住院的15例诊断为病因不明的急性部分横贯性脊髓炎患者进行了一项前瞻性、长期的临床与磁共振成像(MRI)联合随访研究。在平均38.5个月的随访期结束时,15例患者中有12例(80%)发展为临床确诊或实验室支持确诊的多发性硬化症(MS)。发病时头颅MRI显示中枢神经系统脑室周围白质病变,使MS发生的可能性增加到93%。