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

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 atr...

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Autores principales: Leahy, Christopher B, Robinson, Andrew C, Jabbari, Edwin, Morris, Huw R, Lally, Imogen, Djoukhadar, Ibrahim, Roncaroli, Federico, Kobylecki, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084019/
https://www.ncbi.nlm.nih.gov/pubmed/35822248
http://dx.doi.org/10.1111/neup.12848
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author Leahy, Christopher B
Robinson, Andrew C
Jabbari, Edwin
Morris, Huw R
Lally, Imogen
Djoukhadar, Ibrahim
Roncaroli, Federico
Kobylecki, Christopher
author_facet Leahy, Christopher B
Robinson, Andrew C
Jabbari, Edwin
Morris, Huw R
Lally, Imogen
Djoukhadar, Ibrahim
Roncaroli, Federico
Kobylecki, Christopher
author_sort Leahy, Christopher B
collection PubMed
description 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.
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spelling pubmed-100840192023-04-11 A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism Leahy, Christopher B Robinson, Andrew C Jabbari, Edwin Morris, Huw R Lally, Imogen Djoukhadar, Ibrahim Roncaroli, Federico Kobylecki, Christopher Neuropathology Case Reports 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. John Wiley & Sons Australia, Ltd 2022-07-12 2022-12 /pmc/articles/PMC10084019/ /pubmed/35822248 http://dx.doi.org/10.1111/neup.12848 Text en © 2022 The Authors. Neuropathology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Neuropathology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Leahy, Christopher B
Robinson, Andrew C
Jabbari, Edwin
Morris, Huw R
Lally, Imogen
Djoukhadar, Ibrahim
Roncaroli, Federico
Kobylecki, Christopher
A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title_full A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title_fullStr A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title_full_unstemmed A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title_short A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
title_sort case of lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084019/
https://www.ncbi.nlm.nih.gov/pubmed/35822248
http://dx.doi.org/10.1111/neup.12848
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