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Lewy and his inclusion bodies: Discovery and rejection

Fritz Jacob Heinrich Lewy described the pathology of Paralysis agitans [Parkinson disease] and was the first to identify eosinophilic inclusion bodies in neurons of certain brain nuclei, later known as Lewy bodies, the pathological signature of the Lewy body diseases. In 1912, he published his semin...

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Autores principales: Engelhardt, Eliasz, Gomes, Marleide da Mota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710688/
https://www.ncbi.nlm.nih.gov/pubmed/29213511
http://dx.doi.org/10.1590/1980-57642016dn11-020012
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author Engelhardt, Eliasz
Gomes, Marleide da Mota
author_facet Engelhardt, Eliasz
Gomes, Marleide da Mota
author_sort Engelhardt, Eliasz
collection PubMed
description Fritz Jacob Heinrich Lewy described the pathology of Paralysis agitans [Parkinson disease] and was the first to identify eosinophilic inclusion bodies in neurons of certain brain nuclei, later known as Lewy bodies, the pathological signature of the Lewy body diseases. In 1912, he published his seminal study, followed soon after by an update paper, and 10 years later, in 1923, by his voluminous book, where he exhaustively described the subject. The publication provided extensive information on the pathology of Paralysis agitans, and the entirely novel finding of eosinophilic inclusion bodies, which would become widely recognized and debated in the future. His discovery was acknowledged by important researchers who even named the structure after him. However, after his last publication on the issue, inexplicably, he never mentioned his histopathological discovery again. Despite several hypotheses, the reasons that led him to neglect (reject) the structure which he so preeminently described have remained elusive.
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spelling pubmed-57106882017-12-06 Lewy and his inclusion bodies: Discovery and rejection Engelhardt, Eliasz Gomes, Marleide da Mota Dement Neuropsychol History Note Fritz Jacob Heinrich Lewy described the pathology of Paralysis agitans [Parkinson disease] and was the first to identify eosinophilic inclusion bodies in neurons of certain brain nuclei, later known as Lewy bodies, the pathological signature of the Lewy body diseases. In 1912, he published his seminal study, followed soon after by an update paper, and 10 years later, in 1923, by his voluminous book, where he exhaustively described the subject. The publication provided extensive information on the pathology of Paralysis agitans, and the entirely novel finding of eosinophilic inclusion bodies, which would become widely recognized and debated in the future. His discovery was acknowledged by important researchers who even named the structure after him. However, after his last publication on the issue, inexplicably, he never mentioned his histopathological discovery again. Despite several hypotheses, the reasons that led him to neglect (reject) the structure which he so preeminently described have remained elusive. Associação de Neurologia Cognitiva e do Comportamento 2017 /pmc/articles/PMC5710688/ /pubmed/29213511 http://dx.doi.org/10.1590/1980-57642016dn11-020012 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle History Note
Engelhardt, Eliasz
Gomes, Marleide da Mota
Lewy and his inclusion bodies: Discovery and rejection
title Lewy and his inclusion bodies: Discovery and rejection
title_full Lewy and his inclusion bodies: Discovery and rejection
title_fullStr Lewy and his inclusion bodies: Discovery and rejection
title_full_unstemmed Lewy and his inclusion bodies: Discovery and rejection
title_short Lewy and his inclusion bodies: Discovery and rejection
title_sort lewy and his inclusion bodies: discovery and rejection
topic History Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710688/
https://www.ncbi.nlm.nih.gov/pubmed/29213511
http://dx.doi.org/10.1590/1980-57642016dn11-020012
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