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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.
Afiliación
  • Leahy CB; Department of Neurology, Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
  • Robinson AC; Division of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, School of Biological Sciences, University of Manchester, Salford Royal Hospital, Salford, UK.
  • Jabbari E; Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Manchester, UK.
  • Morris HR; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Lally I; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Djoukhadar I; Department of Cellular Pathology, Northern Care Alliance NHS Foundation Trust, Manchester, UK.
  • Roncaroli F; Department of Neuroradiology, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
  • Kobylecki C; Division of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, School of Biological Sciences, University of Manchester, Salford Royal Hospital, Salford, UK.
Neuropathology ; 42(6): 540-547, 2022 Dec.
Article en En | MEDLINE | ID: mdl-35822248
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Atrofia de Múltiples Sistemas / Trastornos Parkinsonianos / Enfermedad por Cuerpos de Lewy Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Atrofia de Múltiples Sistemas / Trastornos Parkinsonianos / Enfermedad por Cuerpos de Lewy Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article