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以额颞叶痴呆为表现的自发性颅内低压:一例报告

Spontaneous Intracranial Hypotension Presenting With Frontotemporal Dementia: A Case Report.

作者信息

Ozyigit Ahmet, Michaelides Costas, Natsiopoulos Konstantinos

机构信息

University of Nicosia Medical School, Nicosia, Cyprus.

Department of Neurology, American Medical Center, Nicosia, Cyprus.

出版信息

Front Neurol. 2018 Aug 17;9:673. doi: 10.3389/fneur.2018.00673. eCollection 2018.

Abstract

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.

摘要

自发性颅内低压(SIH)是一种罕见且常被漏诊的疾病,通常由脑脊液漏引起。SIH的典型临床表现是体位性头痛和头晕。较少见的并发症包括恶心、颈部僵硬,甚至昏迷。本病例报告描述了一名70岁女性,最初主诉为体位性头痛和发作性睡眠,随后出现了长达22个月的人格和行为改变、认知功能减退、尿失禁、舞蹈症和构音障碍的进行性病史。尽管未发现具体的脑脊液漏,但该患者被怀疑患有SIH,在接受2个月的类固醇治疗后症状完全缓解。本病例强调,SIH是包括痴呆在内的多种神经系统症状的罕见且可逆的病因。神经科医生在评估有无法用其他原因解释的神经系统体征和症状的患者时应意识到这一诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32d3/6107704/0d2d6ae076a7/fneur-09-00673-g0001.jpg

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