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Acquired hepatocerebral degeneration

Acquired hepatocerebral degeneration is a rare, mostly irreversible neurological syndrome that occurs in patients with chronic liver disease, particularly in those with surgically or spontaneously induced portosystemic shunts. Typical magnetic resonance findings are T1 hyperintensity in the pallidum...

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Autores principales: Yalçın, Destînâ, Oğuz-Akarsu, Emel, Sökmen, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107273/
https://www.ncbi.nlm.nih.gov/pubmed/27094529
http://dx.doi.org/10.17712/nsj.2016.2.20150164
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author Yalçın, Destînâ
Oğuz-Akarsu, Emel
Sökmen, Mehmet
author_facet Yalçın, Destînâ
Oğuz-Akarsu, Emel
Sökmen, Mehmet
author_sort Yalçın, Destînâ
collection PubMed
description Acquired hepatocerebral degeneration is a rare, mostly irreversible neurological syndrome that occurs in patients with chronic liver disease, particularly in those with surgically or spontaneously induced portosystemic shunts. Typical magnetic resonance findings are T1 hyperintensity in the pallidum, substantia nigra, periaquaductal gray matter. In this paper, we report a case of a 51-year-old woman presented with hepatic encephalopathy episodes and typical magnetic resonance findings, who does not develop any neurological signs or symptoms, nor cognitive decline in the follow up period, lasting for 3 years.
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spelling pubmed-51072732016-11-17 Acquired hepatocerebral degeneration Yalçın, Destînâ Oğuz-Akarsu, Emel Sökmen, Mehmet Neurosciences (Riyadh) Case Report Acquired hepatocerebral degeneration is a rare, mostly irreversible neurological syndrome that occurs in patients with chronic liver disease, particularly in those with surgically or spontaneously induced portosystemic shunts. Typical magnetic resonance findings are T1 hyperintensity in the pallidum, substantia nigra, periaquaductal gray matter. In this paper, we report a case of a 51-year-old woman presented with hepatic encephalopathy episodes and typical magnetic resonance findings, who does not develop any neurological signs or symptoms, nor cognitive decline in the follow up period, lasting for 3 years. Riyadh : Armed Forces Hospital 2016-04 /pmc/articles/PMC5107273/ /pubmed/27094529 http://dx.doi.org/10.17712/nsj.2016.2.20150164 Text en Copyright: © Neurosciences https://creativecommons.org/licenses/by-nc-sa/3.0/Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.
spellingShingle Case Report
Yalçın, Destînâ
Oğuz-Akarsu, Emel
Sökmen, Mehmet
Acquired hepatocerebral degeneration
title Acquired hepatocerebral degeneration
title_full Acquired hepatocerebral degeneration
title_fullStr Acquired hepatocerebral degeneration
title_full_unstemmed Acquired hepatocerebral degeneration
title_short Acquired hepatocerebral degeneration
title_sort acquired hepatocerebral degeneration
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107273/
https://www.ncbi.nlm.nih.gov/pubmed/27094529
http://dx.doi.org/10.17712/nsj.2016.2.20150164
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AT oguzakarsuemel acquiredhepatocerebraldegeneration
AT sokmenmehmet acquiredhepatocerebraldegeneration