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Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma

We report the case of a 72-year-old patient presenting in our ICU with persistent postoperative coma in a context of recent unexplored neurological dysfunction. Detailed medical history taking from the patient’s family revealed he recently suffered from gait instability, urinary incontinence, and sl...

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Detalles Bibliográficos
Autores principales: Saleh, Mohamed, Bouex, Marine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116640/
https://www.ncbi.nlm.nih.gov/pubmed/27917383
http://dx.doi.org/10.3389/fmed.2016.00059
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author Saleh, Mohamed
Bouex, Marine
author_facet Saleh, Mohamed
Bouex, Marine
author_sort Saleh, Mohamed
collection PubMed
description We report the case of a 72-year-old patient presenting in our ICU with persistent postoperative coma in a context of recent unexplored neurological dysfunction. Detailed medical history taking from the patient’s family revealed he recently suffered from gait instability, urinary incontinence, and slight cognitive impairment. These constituted the clinical triad of normal pressure hydrocephalus syndrome. The presence of normal cerebrospinal fluid (CSF) pressure and distinctive radiological findings confirmed the diagnosis of normal pressure hydrocephalus or Hakims–Adams syndrome. After CSF volume subtraction (soustraction), the patient recovered a normal level of consciousness and was successfully weaned from mechanical ventilation. Normal pressure hydrocephalus should be included in the differential diagnosis of delayed postoperative arousal, especially in the elderly.
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spelling pubmed-51166402016-12-02 Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma Saleh, Mohamed Bouex, Marine Front Med (Lausanne) Medicine We report the case of a 72-year-old patient presenting in our ICU with persistent postoperative coma in a context of recent unexplored neurological dysfunction. Detailed medical history taking from the patient’s family revealed he recently suffered from gait instability, urinary incontinence, and slight cognitive impairment. These constituted the clinical triad of normal pressure hydrocephalus syndrome. The presence of normal cerebrospinal fluid (CSF) pressure and distinctive radiological findings confirmed the diagnosis of normal pressure hydrocephalus or Hakims–Adams syndrome. After CSF volume subtraction (soustraction), the patient recovered a normal level of consciousness and was successfully weaned from mechanical ventilation. Normal pressure hydrocephalus should be included in the differential diagnosis of delayed postoperative arousal, especially in the elderly. Frontiers Media S.A. 2016-11-21 /pmc/articles/PMC5116640/ /pubmed/27917383 http://dx.doi.org/10.3389/fmed.2016.00059 Text en Copyright © 2016 Saleh and Bouex. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Saleh, Mohamed
Bouex, Marine
Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title_full Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title_fullStr Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title_full_unstemmed Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title_short Hakim–Adams Syndrome: An Unusual Cause of Reversible Postoperative Coma
title_sort hakim–adams syndrome: an unusual cause of reversible postoperative coma
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116640/
https://www.ncbi.nlm.nih.gov/pubmed/27917383
http://dx.doi.org/10.3389/fmed.2016.00059
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