Wang Huiyuan, Shi Tianming, Shang Yafei, Chen Xinyi, Xu Jie, Geng Yu
Department of Clinical Medicine, Bengbu Medical College, Bengbu, China.
Center for Rehabilitation Medicine, Department of Neurology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital, Hangzhou Medical College), Hangzhou, China.
Front Neurol. 2023 Jan 9;13:1072220. doi: 10.3389/fneur.2022.1072220. eCollection 2022.
Spiller syndrome is a rare subtype of medial medullary infarction (MMI). Herein, we report on a patient with progressing stroke who presented with the initial features of acute peripheral vestibulopathy and MMI (Spiller syndrome), as confirmed by magnetic resonance imaging (MRI). A 42-year-old man experienced acute persistent vertigo with nausea, vomiting, and severe gait instability for 6 h before presenting to the emergency department. He exhibited spontaneous right-beating horizontal-torsional nystagmus that intensified on rightward gaze. The patient fell to the left side during the Romberg test. Cranial computed tomography (CT) performed immediately upon admission did not provide evidence for ischemia or hemorrhage of the brainstem and cerebellum; however, the symptoms underwent exacerbation 4 h after admission, manifesting as left-sided limb weakness and dysarthria, without dysphagia. Furthermore, bedside examination revealed difficulty in extending the tongue to the right, positive left Babinski's sign, and abnormal vibration and position sense in the paralyzed limb. Head impulse test recording revealed a normal gain in the vestibulo-ocular reflex, and numerous consistent covert corrective saccades were captured upon turning the head to the left side. Cranial MRI depicted an acute infarct confined to the right side of the medial medulla, which met the diagnostic criteria for Spiller syndrome. Our study underscores the importance of considering the possibility of a nucleus prepositus hypoglossi lesion even if the signs and symptoms support the diagnosis of peripheral lesions in patients with acute vestibular syndrome exhibiting vascular risk factors.
斯皮勒综合征是延髓内侧梗死(MMI)的一种罕见亚型。在此,我们报告一例进展性卒中患者,其最初表现为急性周围性前庭病和MMI(斯皮勒综合征)的特征,磁共振成像(MRI)证实了这一点。一名42岁男性在前往急诊科就诊前6小时出现急性持续性眩晕,并伴有恶心、呕吐和严重步态不稳。他表现出自发性向右跳动的水平扭转性眼球震颤,向右注视时加剧。在罗姆伯格试验中,患者向左倾倒。入院时立即进行的头颅计算机断层扫描(CT)未发现脑干和小脑缺血或出血的证据;然而,入院4小时后症状加重,表现为左侧肢体无力和构音障碍,无吞咽困难。此外,床边检查发现患者伸舌至右侧困难,左侧巴宾斯基征阳性,瘫痪肢体的振动觉和位置觉异常。头部脉冲试验记录显示前庭眼反射增益正常,向左转头时捕捉到许多一致的隐蔽性矫正扫视。头颅MRI显示急性梗死局限于延髓内侧右侧,符合斯皮勒综合征的诊断标准。我们的研究强调,对于有血管危险因素的急性前庭综合征患者,即使体征和症状支持周围性病变的诊断,也应考虑舌下前置核病变的可能性。