最初被误诊为自身免疫性脑炎的新型致病性 Presenilin 1 变体导致的早发性阿尔茨海默氏症痴呆症

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Nathalia Rossoni Ronchi, Matheus A Castro, Artur M Coutinho, Leandro T Lucato, Guilherme Diogo Silva, Sonia M Brucki, Fernando Kok, Eduardo Sturzeneker Trés, Paulo Ribeiro Nóbrega, Fernando Freua, Ricardo Nitrini, Mateus Mistieri Simabukuro
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引用次数: 0

摘要

目的:预激蛋白 1(PSEN1)的致病变异与早发性阿尔茨海默病(AD)有关,并可能作为新变异出现。与散发性阿尔茨海默病相比,它可能伴有精神症状、癫痫发作、肌阵挛和局灶性表现。由于 PSEN1 可发生于无神经系统疾病家族史的年轻患者,而且这些症状在自身免疫性脑炎(AE)中也很常见,因此诊断可能会被忽视。我们的目的是证明诊断患有模拟 AE 的神经退行性疾病的年轻患者所面临的挑战:我们描述了一例年轻患者的病例,她患有隐匿性进行性痴呆、肌阵挛、癫痫发作和失语,无痴呆家族史,脑部核磁共振成像和脑脊液检查提示神经炎症:她最初被误诊为 AE。经过进一步检查,发现了PSEN1中的一个新的致病变体:本病例表明,对于临床和神经影像学特征不典型的隐匿性进行性痴呆的年轻患者,即使没有神经系统疾病家族史,也必须考虑PSEN1。不遵守已公布的可能和疑似 AE 的标准,以及过度解读 CSF 和 MRI 中细微的炎症发现,都会导致误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Young-Onset Alzheimer Dementia Due to a Novel Pathogenic Presenilin 1 Variant Initially Misdiagnosed as Autoimmune Encephalitis.

Objectives: Pathogenic variants in presenilin 1 (PSEN1) are related to early-onset Alzheimer disease (AD) and may occur as de novo variants. In comparison with sporadic forms, it can present with psychiatric manifestations, seizures, myoclonus, and focal presentation. Because PSEN1 can occur in young patients who lack a family history of neurologic disorders and because these symptoms are also frequent in autoimmune encephalitis (AE), diagnosis may be overlooked. Our aim was to demonstrate the challenge in diagnosing young patients with neurodegenerative diseases that simulate AE.

Methods: We describe a case of a young patient with insidious progressive dementia, myoclonus, seizures, and aphasia, with no family history of dementia, along with signs suggestive of neuroinflammation on brain MRI and CSF examination.

Results: She was initially misdiagnosed as having AE. Further investigation was performed, leading to the discovery of a novel and de novo pathogenic variant in PSEN1.

Discussion: This case demonstrates the importance of considering PSEN1 in young patients with insidious progressive dementia with atypical clinical and neuroimaging features, even in patients without a family history of neurologic disorders. Not adhering to published criteria of possible and probable AE and overinterpretation of subtle inflammatory findings in CSF and MRI contribute to misdiagnosis.

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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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