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Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension

Spontaneous intracranial hypotension (SIH) is a syndrome characterized by low cerebrospinal fluid (CSF) pressure and postural headaches. It is a rare condition which may sometimes present with severe symptoms such as stupor or coma. The standard treatment protocol includes conservative measures such...

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Autores principales: Goto, Shunsaku, Ohshima, Tomotaka, Yamamoto, Taiki, Shimato, Shinji, Nishizawa, Toshihisa, Kato, Kyozo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885822/
https://www.ncbi.nlm.nih.gov/pubmed/27303109
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author Goto, Shunsaku
Ohshima, Tomotaka
Yamamoto, Taiki
Shimato, Shinji
Nishizawa, Toshihisa
Kato, Kyozo
author_facet Goto, Shunsaku
Ohshima, Tomotaka
Yamamoto, Taiki
Shimato, Shinji
Nishizawa, Toshihisa
Kato, Kyozo
author_sort Goto, Shunsaku
collection PubMed
description Spontaneous intracranial hypotension (SIH) is a syndrome characterized by low cerebrospinal fluid (CSF) pressure and postural headaches. It is a rare condition which may sometimes present with severe symptoms such as stupor or coma. The standard treatment protocol includes conservative measures such as bed rest, hydration, and steroids. However, severe cases may require invasive measures such as epidural blood patch (EBP), continuous epidural saline infusion, epidural fibrin glue, or surgical repair of the dural defect. In this report, we describe a case of severe SIH resulting in coma that exhibited dramatic improvement on intravenous administration of steroids. This is the first report of severe SIH causing coma that was treated non-invasively by steroids only.
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spelling pubmed-48858222016-06-14 Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension Goto, Shunsaku Ohshima, Tomotaka Yamamoto, Taiki Shimato, Shinji Nishizawa, Toshihisa Kato, Kyozo Nagoya J Med Sci Case Report Spontaneous intracranial hypotension (SIH) is a syndrome characterized by low cerebrospinal fluid (CSF) pressure and postural headaches. It is a rare condition which may sometimes present with severe symptoms such as stupor or coma. The standard treatment protocol includes conservative measures such as bed rest, hydration, and steroids. However, severe cases may require invasive measures such as epidural blood patch (EBP), continuous epidural saline infusion, epidural fibrin glue, or surgical repair of the dural defect. In this report, we describe a case of severe SIH resulting in coma that exhibited dramatic improvement on intravenous administration of steroids. This is the first report of severe SIH causing coma that was treated non-invasively by steroids only. Nagoya University 2016-05 /pmc/articles/PMC4885822/ /pubmed/27303109 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Goto, Shunsaku
Ohshima, Tomotaka
Yamamoto, Taiki
Shimato, Shinji
Nishizawa, Toshihisa
Kato, Kyozo
Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title_full Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title_fullStr Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title_full_unstemmed Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title_short Successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
title_sort successful steroid treatment of coma induced by severe spontaneous intracranial hypotension
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885822/
https://www.ncbi.nlm.nih.gov/pubmed/27303109
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