Oestmann A, Achtnichts L, Kappos L, Gass A, Naegelin Y
Medizinische Klinik, Universitätsspital Basel.
Dtsch Med Wochenschr. 2008 Jan;133(3):76-8. doi: 10.1055/s-2008-1017477.
A 34-year-old previously healthy woman presented with a five-day history of subacute onset of a numb chin. Examination on admission revealed isolated hypesthesia on the left side of the chin and lower lip.
Brain magnetic resonance imaging (MRI) demonstrated a lesion involving the pontine trigeminal fibers and multiple periventricular T2-hyperintense white matter lesions suggestive of inflammatory /demyelinating disease. Cerebrospinal fluid analysis revealed oligoclonal IgG bands (only in cerebrospinal fluid) and an increased IgG index. A follow-up MRI after four months demonstrated new supratentorial brain lesions, confirming a syndrome, highly suggestive of multiple sclerosis as the likely underlying diagnosis. TREATMENT AND FOLLOW-UP: The facial sensory disturbance resolved spontaneously. Prophylactic treatment with interferon-beta was started.
The numb chin syndrome may be the initial presentation of a clinically isolated syndrome suggestive of multiple sclerosis. Prophylactic immunomodulatory treatment may be started after the suspicion of inflammatory/demyelinating activity is confirmed.
一名34岁既往健康的女性,出现亚急性发作的麻木下巴症状5天。入院检查发现下巴左侧和下唇孤立性感觉减退。
脑部磁共振成像(MRI)显示一个累及脑桥三叉神经纤维的病灶,以及多个脑室周围T2高信号白质病灶,提示炎症性/脱髓鞘疾病。脑脊液分析显示寡克隆IgG带(仅在脑脊液中)和IgG指数升高。4个月后的随访MRI显示幕上出现新的脑部病灶,证实为一种综合征,高度提示多发性硬化症为可能的潜在诊断。
面部感觉障碍自行缓解。开始使用β-干扰素进行预防性治疗。
麻木下巴综合征可能是提示多发性硬化症的临床孤立综合征的初始表现。在确认存在炎症性/脱髓鞘活动的怀疑后,可开始进行预防性免疫调节治疗。