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When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients

OBJECTIVE: To determine ways to improve diagnostic accuracy of multiple system atrophy (MSA), we assessed the diagnostic process in patients who came to autopsy with antemortem diagnosis of MSA by comparing clinical and pathologic features between those who proved to have MSA and those who did not....

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Autores principales: Koga, Shunsuke, Aoki, Naoya, Uitti, Ryan J., van Gerpen, Jay A., Cheshire, William P., Josephs, Keith A., Wszolek, Zbigniew K., Langston, J. William, Dickson, Dennis W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534078/
https://www.ncbi.nlm.nih.gov/pubmed/26138942
http://dx.doi.org/10.1212/WNL.0000000000001807
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author Koga, Shunsuke
Aoki, Naoya
Uitti, Ryan J.
van Gerpen, Jay A.
Cheshire, William P.
Josephs, Keith A.
Wszolek, Zbigniew K.
Langston, J. William
Dickson, Dennis W.
author_facet Koga, Shunsuke
Aoki, Naoya
Uitti, Ryan J.
van Gerpen, Jay A.
Cheshire, William P.
Josephs, Keith A.
Wszolek, Zbigniew K.
Langston, J. William
Dickson, Dennis W.
author_sort Koga, Shunsuke
collection PubMed
description OBJECTIVE: To determine ways to improve diagnostic accuracy of multiple system atrophy (MSA), we assessed the diagnostic process in patients who came to autopsy with antemortem diagnosis of MSA by comparing clinical and pathologic features between those who proved to have MSA and those who did not. We focus on likely explanations for misdiagnosis. METHODS: This is a retrospective review of 134 consecutive patients with an antemortem clinical diagnosis of MSA who came to autopsy with neuropathologic evaluation of the brain. Of the 134 patients, 125 had adequate medical records for review. Clinical and pathologic features were compared between patients with autopsy-confirmed MSA and those with other pathologic diagnoses, including dementia with Lewy bodies (DLB), Parkinson disease (PD), and progressive supranuclear palsy (PSP). RESULTS: Of the 134 patients with clinically diagnosed MSA, 83 (62%) had the correct diagnosis at autopsy. Pathologically confirmed DLB was the most common misdiagnosis, followed by PSP and PD. Despite meeting pathologic criteria for intermediate to high likelihood of DLB, several patients with DLB did not have dementia and none had significant Alzheimer-type pathology. Autonomic failure was the leading cause of misdiagnosis in DLB and PD, and cerebellar ataxia was the leading cause of misdiagnosis in PSP. CONCLUSIONS: The diagnostic accuracy for MSA was suboptimal in this autopsy study. Pathologically confirmed DLB, PD, and PSP were the most common diseases to masquerade as MSA. This has significant implications not only for patient care, but also for research studies in MSA cases that do not have pathologic confirmation.
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spelling pubmed-45340782015-08-21 When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients Koga, Shunsuke Aoki, Naoya Uitti, Ryan J. van Gerpen, Jay A. Cheshire, William P. Josephs, Keith A. Wszolek, Zbigniew K. Langston, J. William Dickson, Dennis W. Neurology Article OBJECTIVE: To determine ways to improve diagnostic accuracy of multiple system atrophy (MSA), we assessed the diagnostic process in patients who came to autopsy with antemortem diagnosis of MSA by comparing clinical and pathologic features between those who proved to have MSA and those who did not. We focus on likely explanations for misdiagnosis. METHODS: This is a retrospective review of 134 consecutive patients with an antemortem clinical diagnosis of MSA who came to autopsy with neuropathologic evaluation of the brain. Of the 134 patients, 125 had adequate medical records for review. Clinical and pathologic features were compared between patients with autopsy-confirmed MSA and those with other pathologic diagnoses, including dementia with Lewy bodies (DLB), Parkinson disease (PD), and progressive supranuclear palsy (PSP). RESULTS: Of the 134 patients with clinically diagnosed MSA, 83 (62%) had the correct diagnosis at autopsy. Pathologically confirmed DLB was the most common misdiagnosis, followed by PSP and PD. Despite meeting pathologic criteria for intermediate to high likelihood of DLB, several patients with DLB did not have dementia and none had significant Alzheimer-type pathology. Autonomic failure was the leading cause of misdiagnosis in DLB and PD, and cerebellar ataxia was the leading cause of misdiagnosis in PSP. CONCLUSIONS: The diagnostic accuracy for MSA was suboptimal in this autopsy study. Pathologically confirmed DLB, PD, and PSP were the most common diseases to masquerade as MSA. This has significant implications not only for patient care, but also for research studies in MSA cases that do not have pathologic confirmation. Lippincott Williams & Wilkins 2015-08-04 /pmc/articles/PMC4534078/ /pubmed/26138942 http://dx.doi.org/10.1212/WNL.0000000000001807 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Article
Koga, Shunsuke
Aoki, Naoya
Uitti, Ryan J.
van Gerpen, Jay A.
Cheshire, William P.
Josephs, Keith A.
Wszolek, Zbigniew K.
Langston, J. William
Dickson, Dennis W.
When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title_full When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title_fullStr When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title_full_unstemmed When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title_short When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients
title_sort when dlb, pd, and psp masquerade as msa: an autopsy study of 134 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534078/
https://www.ncbi.nlm.nih.gov/pubmed/26138942
http://dx.doi.org/10.1212/WNL.0000000000001807
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