Department of Radiology, The First Affiliated Hospital, Chongqing Medical University, Chongqing, 400016, China.
J Neurol. 2011 Feb;258(2):273-6. doi: 10.1007/s00415-010-5748-4. Epub 2010 Sep 18.
Paroxysmal dysarthria (PD) and paroxysmal dysarthria-ataxia (PDA) syndromes are uncommon symptoms of the neurological dysfunction in multiple sclerosis (MS). We describe two patients who had clinically definite MS presented with symptomatic PD and PDA syndromes, respectively, related to demyelinating lesions. In one patient, the PD symptom was the initial manifestation of an acute episode. In the other patient, the episode of dysarthria was accompanied by ataxia disorders. Both patients had midbrain lesions at or below the level of the right red nucleus on magnetic resonance imaging (MRI), confirming that this area is critically involved. Both responded well to carbamazepine (CBZ).
发作性构音障碍(PD)和发作性构音障碍-共济失调(PDA)综合征是多发性硬化症(MS)神经功能障碍的罕见症状。我们描述了两名分别患有临床确诊多发性硬化症且出现症状性 PD 和 PDA 综合征的患者,这些症状与脱髓鞘病变有关。在一名患者中,PD 症状是急性发作的初始表现。在另一名患者中,构音障碍发作伴有共济失调障碍。两名患者的磁共振成像(MRI)均显示中脑病变位于或低于右侧红核水平,证实该区域受到严重影响。两人均对卡马西平(CBZ)反应良好。