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An unusual stroke-like clinical presentation of Creutzfeldt-Jakob disease: acute vestibular syndrome

机译:Creutzfeldt-Jakob病的异常中风样临床表现:急性前庭综合征

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INTRODUCTIONududVertigo and dizziness are common neurological symptoms in general practice. Most patients have benign peripheral vestibular disorders, but some have dangerous central causes. Recent research has shown that bedside oculomotor examinations accurately discriminate central from peripheral lesions in those with new, acute, continuous vertigo/dizziness with nausea/vomiting, gait unsteadiness, and nystagmus, known as the acute vestibular syndrome.ududCASE REPORTududA 56-year-old man presented to the emergency department with acute vestibular syndrome for 1 week. The patient had no focal neurological symptoms or signs. The presence of direction-fixed, horizontal nystagmus suppressed by visual fixation without vertical ocular misalignment (skew deviation) was consistent with an acute peripheral vestibulopathy, but bilaterally normal vestibuloocular reflexes, confirmed by quantitative horizontal head impulse testing, strongly indicated a central localization. Because of a long delay in care, the patient left the emergency department without treatment. He returned 1 week later with progressive gait disturbance, limb ataxia, myoclonus, and new cognitive deficits. His subsequent course included a rapid neurological decline culminating in home hospice placement and death within 1 month. Magnetic resonance imaging revealed restricted diffusion involving the basal ganglia and cerebral cortex. Spinal fluid 14-3-3 protein was elevated. The rapidly progressive clinical course with dementia, ataxia, and myoclonus plus corroborative neuroimaging and spinal fluid findings confirmed a clinicoradiographic diagnosis of Creutzfeldt-Jacob disease.ududCONCLUSIONSududTo our knowledge, this is the first report of an initial presentation of Creutzfeldt-Jacob disease closely mimicking vestibular neuritis, expanding the known clinical spectrum of prion disease presentations. Despite the initial absence of neurological signs, the central lesion location was differentiated from a benign peripheral vestibulopathy at the first visit using simple bedside vestibular tests. Familiarity with these tests could help providers prevent initial misdiagnosis of important central disorders in patients presenting vertigo or dizziness.
机译:引言 ud ud眩晕和头晕是一般实践中常见的神经系统症状。大多数患者患有良性外周前庭疾病,但有些患者具有危险的中枢病因。最近的研究表明,床旁动眼检查可以准确地区分新发的,急性的,持续性的眩晕/头晕,恶心/呕吐,步态不稳和眼球震颤的患者,称为急性前庭综合征。 ud ud病例报告 ud ud一名56岁的男子因急性前庭综合症出现在急诊室,为期1周。该患者无局灶性神经系统症状或体征。通过视觉固定抑制了方向固定的水平眼球震颤,没有垂直眼错位(偏斜),这与急性外周前庭病变一致,但是通过定量水平头部冲动测试证实的双侧正常前庭反射非常有力地表明了中央局限性。由于护理时间长,该患者未经治疗便离开急诊室。 1周后,他因进行性步态障碍,四肢共济失调,肌阵挛和新的认知缺陷而返回。他的后续课程包括迅速的神经功能衰退,最终导致家庭临终关怀安置并在1个月内死亡。磁共振成像显示受限扩散涉及基底神经节和大脑皮层。脊髓液14-3-3蛋白升高。快速进展的临床过程包括痴呆,共济失调和肌阵挛,加上确诊的神经影像学和脊髓液发现,证实了克罗伊茨费尔特-雅各布病的临床放射学诊断。 ud ud结论 ud ud据我们所知,这是首次报告Creutzfeldt-Jacob病紧密模仿前庭神经炎,扩大了已知的clinical病毒疾病临床表现范围。尽管最初没有神经系统症状,但在初次就诊时使用简单的床旁前庭试验将中心病变位置与良性周围性前庭病变区分开。熟悉这些测试可以帮助提供者防止出现眩晕或头晕的患者对重要中枢疾病的初步误诊。

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