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酷似路易体痴呆的额颞叶痴呆

Frontotemporal dementia mimicking dementia with Lewy bodies.

作者信息

Claassen Daniel O, Parisi Joseph E, Giannini Caterina, Boeve Bradley F, Dickson Dennis W, Josephs Keith A

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA

出版信息

Cogn Behav Neurol. 2008 Sep;21(3):157-63. doi: 10.1097/WNN.0b013e3181864a09.

Abstract

BACKGROUND

Some patients with frontotemporal dementia (FTD) have concomitant extrapyramidal symptoms and psychosis and may simultaneously meet consensus criteria for FTD and for dementia with Lewy bodies (DLB). Clinicopathologic studies are helpful in understanding the underlying neurodegenerative process in such cases.

OBJECTIVE

To describe clinical and pathologic features of 6 patients with signs and symptoms suggestive of both a diagnosis of FTD and DLB at first clinical presentation, of which 2 patients have now undergone autopsy, and to compare them with autopsy-confirmed FTD and Lewy body disease patients.

RESULTS

All 6 patients met published consensus criteria for a diagnosis of both FTD and DLB (5 probable and 1 possible). Clinical symptoms of FTD included personality and behavioral changes, whereas those suggestive of DLB included Parkinsonism, fluctuating cognition, parasomnia, and hallucinations. Five patients underwent single photon emission computed tomography ((99m)Tc) imaging, which showed varying degrees of frontal lobe hypoperfusion. Magnetic resonance imaging, electroencephalogram, and electromyogram were not helpful in differentiating FTD from DLB. Histologic examination of the 2 autopsy cases was consistent with a pathologic diagnosis of TDP-43 proteinopathy; specifically frontotemporal lobar degeneration with ubiquitin-only immunoreactive changes, type 1. There were significant differences between these 6 patients and the 2 groups of autopsy confirmed FTD and Lewy body disease patients.

CONCLUSIONS

We have identified a novel group of FTD patients with clinical features that overlap with DLB, yet seem to be different from both typical FTD and typical Lewy body disease.

摘要

背景

一些额颞叶痴呆(FTD)患者伴有锥体外系症状和精神病,可能同时符合FTD和路易体痴呆(DLB)的共识标准。临床病理研究有助于理解此类病例潜在的神经退行性变过程。

目的

描述6例初诊时具有提示FTD和DLB诊断的体征和症状的患者的临床和病理特征,其中2例患者现已接受尸检,并将他们与尸检确诊的FTD和路易体病患者进行比较。

结果

所有6例患者均符合已发表的FTD和DLB诊断的共识标准(5例可能,1例疑似)。FTD的临床症状包括人格和行为改变,而提示DLB的症状包括帕金森症、认知波动、异态睡眠和幻觉。5例患者接受了单光子发射计算机断层扫描((99m)Tc)成像,显示额叶不同程度的灌注不足。磁共振成像、脑电图和肌电图对区分FTD和DLB无帮助。2例尸检病例的组织学检查与TDP-43蛋白病的病理诊断一致;具体为仅伴有泛素免疫反应性改变的额颞叶变性,1型。这6例患者与2组尸检确诊的FTD和路易体病患者之间存在显著差异。

结论

我们发现了一组具有与DLB重叠的临床特征但似乎不同于典型FTD和典型路易体病的新型FTD患者。

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