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一例以非典型帕金森病为表现的路易体病和间变性星形细胞瘤。

A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism.

机构信息

Department of Neurology, Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.

Division of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, School of Biological Sciences, University of Manchester, Salford Royal Hospital, Salford, UK.

出版信息

Neuropathology. 2022 Dec;42(6):540-547. doi: 10.1111/neup.12848. Epub 2022 Jul 12.

Abstract

We report on a patient with atypical parkinsonism due to coexistent Lewy body disease (LBD) and diffuse anaplastic astrocytoma. The patient presented with a mixed cerebellar and parkinsonian syndrome, incomplete levodopa response, and autonomic failure. The clinical diagnosis was multiple system atrophy (MSA). Supportive features of MSA according to the consensus diagnostic criteria included postural instability and early falls, early dysphagia, pyramidal signs, and orofacial dystonia. Multiple exclusion criteria for a diagnosis of idiopathic Parkinson's disease (iPD) were present. Neuropathological examination of the left hemisphere and the whole midbrain and brainstem revealed LBD, neocortical-type consistent with iPD, hippocampal sclerosis, and widespread neoplastic infiltration by an anaplastic astrocytoma without evidence of a space occupying lesion. There were no pathological features of MSA. The classification of atypical parkinsonism was difficult in this patient. The clinical features and disease course were confounded by the coexistent tumor, leading to atypical presentation and a diagnosis of MSA. We suggest that the initial features were due to Lewy body pathology, while progression and ataxia, pyramidal signs, and falls were accelerated by the occurrence of the astrocytoma. Our case reflects the challenges of an accurate diagnosis of atypical parkinsonism, the potential for confounding co-pathology and the need for autopsy examination to reach a definitive diagnosis.

摘要

我们报告了一例同时患有路易体病(LBD)和弥漫性间变星形细胞瘤的非典型帕金森病患者。该患者表现为混合性小脑和帕金森综合征,左旋多巴反应不完全,自主神经衰竭。临床诊断为多系统萎缩(MSA)。根据共识诊断标准,MSA 的支持特征包括姿势不稳和早期跌倒、早期吞咽困难、锥体束征和口面肌张力障碍。存在许多排除特发性帕金森病(iPD)诊断的标准。左侧大脑半球和整个中脑及脑干的神经病理学检查显示 LBD、符合 iPD 的新皮质型、海马硬化和广泛的间变星形细胞瘤浸润,无占位病变的证据。没有 MSA 的病理特征。该患者的非典型帕金森病分类较为困难。共存的肿瘤使临床特征和病程复杂化,导致非典型表现和 MSA 的诊断。我们推测初始特征归因于路易体病理学,而进展和共济失调、锥体束征和跌倒则加速了星形细胞瘤的发生。我们的病例反映了准确诊断非典型帕金森病的挑战、共存的共病病理学的潜在影响,以及需要尸检检查以做出明确诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/10084019/32247c6a5f7d/NEUP-42-540-g001.jpg

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