Giroud M, Semama D, Pradeaux L, Gouyon J B, Dumas R, Nivelon J L
Service de Neurologie, Hôpital Général, Dijon, France.
Childs Nerv Syst. 1990 Jun;6(4):236-8. doi: 10.1007/BF01850982.
The authors report a case of a 15-month-old infant who presented a left hemiballismus associated with left Marcus-Gunn pupil, and retrobulbar optic neuritis, which disappeared spontaneously in 7 days. Six weeks later, the infant experienced a mild paraparesis with a palsy of the left sixth cranial nerve, which disappeared following steroid therapy. Evoked visual potentials elicited abnormal latencies; cerebrospinal fluid (CSF) showed a rise in white cells and oligoclonal bands. According to the usual classification, this case corresponds to definite multiple sclerosis. The fact that hemiballismus was the initial clinical feature in an infant makes this observation very interesting. In the literature, eight cases of hemiballismus in patients with multiple sclerosis are reported; however, only two cases of multiple sclerosis in infancy have been published, making our case report of particular interest.
作者报告了一例15个月大的婴儿,该婴儿出现了与左侧Marcus-Gunn瞳孔和球后视神经炎相关的左侧偏身颤搐症,症状在7天内自发消失。六周后,婴儿出现轻度双侧下肢轻瘫伴左侧第六颅神经麻痹,经类固醇治疗后消失。视觉诱发电位显示潜伏期异常;脑脊液(CSF)显示白细胞增多和寡克隆带。根据通常的分类,该病例符合明确的多发性硬化症。偏身颤搐症作为婴儿的初始临床特征这一事实使得该观察结果非常有趣。在文献中,报道了8例多发性硬化症患者出现偏身颤搐症的病例;然而,仅发表了2例婴儿期多发性硬化症病例,这使得我们的病例报告特别引人关注。