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Fahr 病与路易体痴呆的临床病理共存。

Clinicopathological co-occurrence of Fahr's disease and dementia with Lewy bodies.

出版信息

Clin Neuropathol. 2020 Sep/Oct;39(5):227-231. doi: 10.5414/NP301267.

Abstract

We present the clinicopathological findings of a case of combined Fahr's disease (FD) and dementia with Lewy bodies (DLB), associated with a novel pathogenic mutation. The patient presented with visual hallucinations, fluctuating confusion and parkinsonism, leading to a presumptive diagnosis of DLB. CT scan showed extensive bilateral parenchymal calcifications, suggestive of FD. DNA sequencing identified a novel missense variant (c.92A>T p.(Asn31Ile)) in the SLC20A2 gene, a gene known to be associated with FD. This change has not been previously recorded in genetic repositories, and in silico analyses classified it as likely to be disease-causing. The patient died aged 77, four years after symptom onset. Neuropathological examination revealed, macroscopically and microscopically, extensive calcification in the striatum, globus and cerebellar white matter. There was also neuronal loss in the substantia nigra and residual neurones contained alpha-synuclein-positive Lewy bodies. The neuropathology was therefore consistent with DLB and FD. A literature review identified 3 other cases of co-existing Fahr's and Lewy body pathology, thus the frequency of dual pathology (44%) is higher than expected by random association. Further studies are needed to determine whether alpha-synucleinopathy is linked mechanistically to FD and/or represents a phenotypic subtype.

摘要

我们呈现了一例 Fahr 病(FD)和路易体痴呆(DLB)合并的临床病理发现,该病例与一种新的致病性突变相关。患者表现出幻视、波动的意识混乱和帕金森病,导致疑似 DLB 的诊断。CT 扫描显示广泛的双侧实质钙化,提示 FD。DNA 测序在 SLC20A2 基因中发现了一种新的错义变异(c.92A>T p.(Asn31Ile)),该基因与 FD 相关。该变化以前未在遗传库中记录,并且计算机分析将其归类为可能导致疾病的变异。患者在症状出现四年后,于 77 岁时死亡。神经病理学检查显示,纹状体、苍白球和小脑白质广泛钙化,黑质神经元丢失,残留神经元含有 alpha-synuclein 阳性路易体。因此,神经病理学与 DLB 和 FD 一致。文献回顾确定了另外 3 例 Fahr's 和 Lewy 体病共存的病例,因此双重病理学(44%)的频率高于随机关联的预期。需要进一步的研究来确定 alpha-synucleinopathy 是否与 FD 有机制上的联系,或者是否代表一种表型亚型。

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