Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.
Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.
J Stroke Cerebrovasc Dis. 2020 Aug;29(8):104806. doi: 10.1016/j.jstrokecerebrovasdis.2020.104806. Epub 2020 May 17.
A 65-year-old man with a history of Wallenberg syndrome caused by vertebral artery dissection at 62 years old was admitted to our hospital with nausea, vertigo, right facial dysesthesia, right hemiplegia, crossed sensory disturbance (sensory loss and numbness in the right face and left body below the neck), and right limb ataxia. Magnetic resonance imaging (MRI) performed 80 minutes after onset revealed no acute ischemic stroke lesions, but magnetic resonance angiography (MRA) demonstrated complete occlusion of the right vertebral artery. Based on these neurological and MRA findings, atypical lateral medullary infarction was suggested, and intravenous tissue plasminogen activator (IV-tPA) was started 178 minutes after onset. Right hemiplegia improved immediately after IV-tPA administration. MRI performed on hospital day 2 showed an acute ischemic lesion on the right side of the medulla oblongata, resulting in a diagnosis of Opalski syndrome. Opalski syndrome is a rare subtype of Wallenberg syndrome accompanied by hemiplegia of the side ipsilateral to the lesion, and expansion of the stroke lesion to the corticospinal tract below the pyramidal decussation is considered to cause ipsilateral hemiplegia. Based on this case and previous reports, Opalski syndrome should be considered when limb ataxia and crossed sensory deficit are observed among patients with hyperacute-onset hemiplegia, and IV t-PA therapy should be considered even in the absence of neurological findings such as dysphagia, dysarthria, and Horner's signs and radiological evidence of acute ischemic stroke.
一位 65 岁男性,62 岁时因椎动脉夹层导致 Wallenberg 综合征,此次因恶心、眩晕、右侧面部感觉异常、右侧偏瘫、交叉感觉障碍(右侧面部和颈部以下左侧身体感觉丧失和麻木)和右侧肢体共济失调入院。发病后 80 分钟进行的磁共振成像(MRI)未显示急性缺血性脑卒中病灶,但磁共振血管造影(MRA)显示右侧椎动脉完全闭塞。根据这些神经学和 MRA 发现,提示为非典型延髓外侧梗死,发病后 178 分钟开始给予静脉组织型纤溶酶原激活剂(IV-tPA)。IV-tPA 给药后右侧偏瘫立即改善。发病后第 2 天的 MRI 显示右侧延髓急性缺血性病灶,诊断为 Opalski 综合征。Opalski 综合征是 Wallenberg 综合征的一种罕见亚型,伴有病变侧偏瘫,扩展到锥体交叉下方的皮质脊髓束被认为导致同侧偏瘫。基于该病例和以往报告,当超急性发作偏瘫患者出现肢体共济失调和交叉感觉缺失时,应考虑 Opalski 综合征,即使没有吞咽困难、构音障碍、Horner 征和急性缺血性脑卒中的影像学证据,也应考虑 IV-tPA 治疗。