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直面难题:一例由皮质基底节变性导致的原发性进行性言语失用症?

Coming to Terms with a Conundrum: A Case of Primary Progressive Apraxia of Speech due to Corticobasal Degeneration?

作者信息

Karantzoulis Aristotelis, Susani Emanuela, Ferrarese Carlo, Appollonio Ildebrando, Tremolizzo Lucio

机构信息

Neurology Unit "San Gerardo" Hospital and University of Milano-Bicocca, Monza, Italy.

Neurology Unit, "Niguarda" hospital, Milano, Italy.

出版信息

Case Rep Neurol. 2021 Jul 20;13(2):483-489. doi: 10.1159/000517367. eCollection 2021 May-Aug.

Abstract

Primary progressive apraxia of speech (PPAOS) is a progressive disorder impairing the motor speech act leaving linguistic function unattained. Although apraxia of speech frequently co-occurs with other neurodegenerative conditions, PPAOS defines a clinical syndrome where apraxia of speech is the sole or prominent symptom for much of the disease's natural history. Mounting evidence is beginning to fully define this disease as the epiphenomenon of 4-repeat (4R) tau pathology although other pathologic signatures have been reported. Indeed, PPAOS patients generally present a parkinsonian syndrome late into their natural history mostly qualifying for either corticobasal syndrome (CBS) or progressive supranuclear palsy (PSP). This is starting to be reflected in diagnostic criteria for PSP, namely, in the PSP speech and language (SL) subcategory; however, this inclusion is not reflected for CBS. Here, we present a single case of a patient with PPAOS and her clinical follow-up lasting 6 years, from the time she sought our attention to her death which occurred 8 years into the disease. PPAOS was the only and prominent symptom for most of the illness with extrapyramidal signs overtly presenting in the last months of its course. Clinical evaluation, imaging, genetic, and cerebrospinal fluid biomarkers all pointed toward an underlying CBD pathology, albeit the eventual anatomopathological confirmation was not performed. Had her clinical course been more suggestive of PSP, she would have qualified for criteria as PSP-SL. Our case therefore suggests the hypothetic need to discuss the broadening of the existing CBS criteria to encompass isolated PPAOS.

摘要

原发性进行性言语失用症(PPAOS)是一种进行性疾病,会损害言语运动行为,而语言功能不受影响。尽管言语失用症经常与其他神经退行性疾病同时出现,但PPAOS定义了一种临床综合征,在该疾病的自然病程中,言语失用症是唯一或突出的症状。越来越多的证据开始将这种疾病完全定义为4重复(4R)tau蛋白病变的附带现象,尽管也有其他病理特征的报道。事实上,PPAOS患者在其自然病程后期通常会出现帕金森综合征,大多符合皮质基底节综合征(CBS)或进行性核上性麻痹(PSP)的诊断标准。这一点开始反映在PSP的诊断标准中,即在PSP言语和语言(SL)亚类中;然而,CBS的诊断标准中并未体现这一点。在此,我们报告一例PPAOS患者及其6年的临床随访情况,从她引起我们的注意到疾病发生8年后去世。在病程的大部分时间里,PPAOS是唯一且突出的症状,锥体外系症状在病程的最后几个月才明显出现。临床评估、影像学、基因和脑脊液生物标志物均指向潜在的皮质基底节变性(CBD)病理改变,尽管最终未进行解剖病理学确诊。如果她的临床病程更符合PSP的表现,她就符合PSP-SL的诊断标准。因此,我们的病例表明,可能需要讨论扩大现有的CBS诊断标准,以涵盖孤立性PPAOS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/392c/8339446/1844360e2a75/crn-0013-0483-g01.jpg

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