Department of Neurological, Behavioural and Neurosurgical Sciences, Section of Neurological Sciences, University of Siena, Viale Bracci 2, 53100, Siena, Italy.
Neurol Sci. 2009 Aug;30(4):329-32. doi: 10.1007/s10072-009-0092-0. Epub 2009 May 15.
Occurrence of multiple sclerosis (MS) in patients with ankylosing spondylitis (AS) has been reported in isolated cases. We describe a white 33-year-old male with a definite familial HLAB27 positive AS and MS-like syndrome. The patient developed acute onset of gait difficulty, postural unsteadiness, dysarthria and right side weakness that resolved within 1 month; after 6 months he presented right-sided face sensory loss, disappeared after 2 weeks. Brain and cervical MRI was performed twice and showed disseminated lesions in space (multiple foci of increased signal intensity in the periventricular white matter, in the corpus callosum, in the hypothalamus, in the brainstem and in the cervical spinal cord) and in time (a new enhancing lesion >3 months after the onset of the clinical event). Visual evoked potentials were markedly altered. Cerebrospinal fluid examination was negative for intrathecal production of oligoclonal bands. Differential diagnosis was considered and other pathologies were excluded.
多发性硬化症(MS)在强直性脊柱炎(AS)患者中的发生已有个案报道。我们描述了一位 33 岁的白人男性,他患有明确的家族性 HLA-B27 阳性 AS 和类似 MS 的综合征。该患者突发步态困难、姿势不稳、构音障碍和右侧无力,1 个月内缓解;6 个月后出现右侧面部感觉丧失,2 周后消失。两次进行了脑部和颈椎 MRI 检查,显示在空间(脑室周围白质、胼胝体、下丘脑、脑干和颈脊髓多个焦点信号强度增加)和时间(临床事件发生后>3 个月出现新的强化病灶)上存在弥散性病变。视觉诱发电位明显改变。脑脊液检查未见鞘内寡克隆带产生。考虑了鉴别诊断并排除了其他病理学。