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Spontaneous Intracranial Hypotension Presenting With Frontotemporal Dementia: A Case Report

机译:自发性颅内低血压合并额颞叶痴呆:一例报告

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摘要

Spontaneous intracranial hypotension (SIH) is a rare and often underdiagnosed condition, which commonly results from a cerebrospinal fluid leak. The classic clinical presentation of SIH is a postural headache and dizziness. Less frequent complications include nausea, neck stiffness, and even coma. This case report describes a 70-year-old woman with an initial complaint of postural headaches and sleep attacks, who developed a 22-month progressive history of personality and behavioral changes, cognitive decline, urinary incontinence, chorea, and dysarthria. Although no specific cerebrospinal fluid leak was identified, the patient was suspected of having SIH and her symptoms completely reversed after a 2-month course of steroids. This case highlights that SIH represents a rare and reversible cause of a wide spectrum of neurological symptoms, including dementia. Neurologists should be aware of this diagnosis when evaluating patients with neurological signs and symptoms that cannot otherwise be explained.
机译:自发性颅内低血压(SIH)是一种罕见且常常被诊断不足的疾病,通常是由于脑脊液漏出引起的。 SIH的经典临床表现是姿势性头痛和头晕。较少见的并发症包括恶心,颈部僵硬,甚至昏迷。该病例报告描述了一名70岁的女性,最初主诉姿势性头痛和睡眠发作,其发展了22个月的人格和行为改变,认知能力下降,尿失禁,舞蹈症和构音障碍的进展史。尽管未发现具体的脑脊液渗漏,但该患者被怀疑患有SIH,并且在接受2个月的类固醇治疗后症状完全消失。该病例表明,SIH代表了广泛的神经系统症状(包括痴呆)的罕见且可逆的原因。当评估具有其他无法解释的神经系统体征和症状的患者时,神经科医师应意识到这种诊断。

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