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A Case of Adult Polyglucosan Body Disease

Adult polyglucosan body disease (APBD) is a rare neurological disease, characterized by adult onset (fifth to seventh decades), progressive sensorimotor or pure motor peripheral neuropathy, upper motor neuron symptoms, neurogenic bladder, and cognitive impairment. APBD is confirmed by a sural nerve...

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Detalles Bibliográficos
Autores principales: Lee, Seung-Yeob, Park, Jae-Hyeon, Kim, Se Hun, Kim, Tai-Seung, Kim, Won-Joo, Choi, Young-Chul
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628064/
https://www.ncbi.nlm.nih.gov/pubmed/17722245
http://dx.doi.org/10.3349/ymj.2007.48.4.701
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author Lee, Seung-Yeob
Park, Jae-Hyeon
Kim, Se Hun
Kim, Tai-Seung
Kim, Won-Joo
Choi, Young-Chul
author_facet Lee, Seung-Yeob
Park, Jae-Hyeon
Kim, Se Hun
Kim, Tai-Seung
Kim, Won-Joo
Choi, Young-Chul
author_sort Lee, Seung-Yeob
collection PubMed
description Adult polyglucosan body disease (APBD) is a rare neurological disease, characterized by adult onset (fifth to seventh decades), progressive sensorimotor or pure motor peripheral neuropathy, upper motor neuron symptoms, neurogenic bladder, and cognitive impairment. APBD is confirmed by a sural nerve biopsy that shows the widespread presence of polyglucosan bodies in the nerve. We report a 70 year old male patient who exhibited progressive weakness in all extremities and dementia. His electrodiagnostic studies showed sensorimotor polyneuropathy and muscle pathology that consisted of polyglucosan bodies located in small peripheral nerves. This is the first case of APBD reported in Korea.
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spelling pubmed-26280642009-02-02 A Case of Adult Polyglucosan Body Disease Lee, Seung-Yeob Park, Jae-Hyeon Kim, Se Hun Kim, Tai-Seung Kim, Won-Joo Choi, Young-Chul Yonsei Med J Case Report Adult polyglucosan body disease (APBD) is a rare neurological disease, characterized by adult onset (fifth to seventh decades), progressive sensorimotor or pure motor peripheral neuropathy, upper motor neuron symptoms, neurogenic bladder, and cognitive impairment. APBD is confirmed by a sural nerve biopsy that shows the widespread presence of polyglucosan bodies in the nerve. We report a 70 year old male patient who exhibited progressive weakness in all extremities and dementia. His electrodiagnostic studies showed sensorimotor polyneuropathy and muscle pathology that consisted of polyglucosan bodies located in small peripheral nerves. This is the first case of APBD reported in Korea. Yonsei University College of Medicine 2007-08-31 2007-08-20 /pmc/articles/PMC2628064/ /pubmed/17722245 http://dx.doi.org/10.3349/ymj.2007.48.4.701 Text en Copyright © 2007 The Yonsei University College of Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lee, Seung-Yeob
Park, Jae-Hyeon
Kim, Se Hun
Kim, Tai-Seung
Kim, Won-Joo
Choi, Young-Chul
A Case of Adult Polyglucosan Body Disease
title A Case of Adult Polyglucosan Body Disease
title_full A Case of Adult Polyglucosan Body Disease
title_fullStr A Case of Adult Polyglucosan Body Disease
title_full_unstemmed A Case of Adult Polyglucosan Body Disease
title_short A Case of Adult Polyglucosan Body Disease
title_sort case of adult polyglucosan body disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628064/
https://www.ncbi.nlm.nih.gov/pubmed/17722245
http://dx.doi.org/10.3349/ymj.2007.48.4.701
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