Zhou Chenguang, He Yuanhong, Chao Zhiwen, Zhu Yinghui, Wang Peng, Wang Xingping, Liu Shanshan, Han Wei, Wang Jianping
Department of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Front Neurol. 2017 Aug 3;8:376. doi: 10.3389/fneur.2017.00376. eCollection 2017.
Wernekink commissure syndrome secondary to caudal paramedian midbrain infarction (CPMI) is a rare midbrain syndrome involving the decussation of the superior cerebellar peduncle in the caudal paramedian midbrain tegmentum. The central characteristics are constant bilateral cerebellar dysfunction, variable eye movement disorders, and rare delayed palatal myoclonus. Following is a description of the case of a 60-year-old man who presented with dizziness, slurred speech, and difficulty walking. Neurological examination revealed bilateral cerebellar dysfunction and bilateral internuclear ophthalmoplegia (bilateral INO). Serial magnetic resonance imaging (MRI) revealed a lesion in the caudal paramedian midbrain with a "heart-shaped" sign on fluid-attenuation inversion recovery images and a "V-shaped" appearance on diffusion-weighted imaging (DWI). An acute CPMI with a "heart or V" appearance sign was diagnosed. Upon follow-up evaluation 3 months later, a palatal tremor accompanied by involuntary head tremor was discovered. Hypertrophy and increased signal of the bilateral inferior olivary nucleus, compatible with hypertropic olivary degeneration (HOD) were revealed during a subsequent MRI study.
尾侧中脑梗死(CPMI)继发的Wernekink交叉综合征是一种罕见的中脑综合征,累及尾侧中脑被盖部的小脑上脚交叉。其主要特征为持续性双侧小脑功能障碍、多变的眼球运动障碍以及罕见的迟发性腭肌阵挛。以下是一名60岁男性患者的病例描述,该患者出现头晕、言语不清和行走困难。神经系统检查发现双侧小脑功能障碍和双侧核间性眼肌麻痹(双侧INO)。系列磁共振成像(MRI)显示尾侧中脑有一病灶,在液体衰减反转恢复图像上呈“心形”征,在弥散加权成像(DWI)上呈“V形”外观。诊断为具有“心或V”外观征的急性CPMI。3个月后的随访评估发现伴有不自主头部震颤的腭震颤。随后的MRI研究显示双侧下橄榄核肥大且信号增强,符合肥大性橄榄核变性(HOD)。