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Guillain-Barre syndrome with posterior reversible encephalopathy syndrome
Posterior reversible encephalopathy syndrome (PRES) is a clinicoradiologic entity commonly associated with eclampsia, septicemia, chemotherapeutic drugs etc. Concurrent occurrence of Guillain-Barre syndrome (GBS) with PRES is a rare entity. Dysautonomia is a proposed mechanism for such occurrence. H...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985363/ https://www.ncbi.nlm.nih.gov/pubmed/24741255 http://dx.doi.org/10.4103/0976-3147.127877 |
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author | Banakar, Basavaraj F. Pujar, Guruprasad S. Bhargava, Amita Khichar, Shubhkaran |
author_facet | Banakar, Basavaraj F. Pujar, Guruprasad S. Bhargava, Amita Khichar, Shubhkaran |
author_sort | Banakar, Basavaraj F. |
collection | PubMed |
description | Posterior reversible encephalopathy syndrome (PRES) is a clinicoradiologic entity commonly associated with eclampsia, septicemia, chemotherapeutic drugs etc. Concurrent occurrence of Guillain-Barre syndrome (GBS) with PRES is a rare entity. Dysautonomia is a proposed mechanism for such occurrence. Here we present a non-diabetic, non-hypertensive 63-year-old male patient, who came with acute onset flaccid quadriparesis, developing generalized seizures, altered sensorium and raised blood pressure on fifth day of illness. Magnetic resonance imaging (MRI) of brain showed altered signal intensities involving the parieto-occipital areas suggestive of posterior reversible encephalopathy. Cerebrospinal fluid analysis showed albuminocytological dissociation, nerve conduction studies revealed demyelinating type of polyneuropathy. The patient was treated with antihypertensives and antiepileptics. After resolution of the encephalopathy, intravenous immunoglobulin (IVIg) was given. The patient recovered gradually over few months. Our case concludes GBS as independent risk factor, for PRES may be secondary to dysautonomia and physicians should be aware of such rare coexistence so that early treatment can be done to reduce the mortality and morbidity. |
format | Online Article Text |
id | pubmed-3985363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39853632014-04-16 Guillain-Barre syndrome with posterior reversible encephalopathy syndrome Banakar, Basavaraj F. Pujar, Guruprasad S. Bhargava, Amita Khichar, Shubhkaran J Neurosci Rural Pract Case Report Posterior reversible encephalopathy syndrome (PRES) is a clinicoradiologic entity commonly associated with eclampsia, septicemia, chemotherapeutic drugs etc. Concurrent occurrence of Guillain-Barre syndrome (GBS) with PRES is a rare entity. Dysautonomia is a proposed mechanism for such occurrence. Here we present a non-diabetic, non-hypertensive 63-year-old male patient, who came with acute onset flaccid quadriparesis, developing generalized seizures, altered sensorium and raised blood pressure on fifth day of illness. Magnetic resonance imaging (MRI) of brain showed altered signal intensities involving the parieto-occipital areas suggestive of posterior reversible encephalopathy. Cerebrospinal fluid analysis showed albuminocytological dissociation, nerve conduction studies revealed demyelinating type of polyneuropathy. The patient was treated with antihypertensives and antiepileptics. After resolution of the encephalopathy, intravenous immunoglobulin (IVIg) was given. The patient recovered gradually over few months. Our case concludes GBS as independent risk factor, for PRES may be secondary to dysautonomia and physicians should be aware of such rare coexistence so that early treatment can be done to reduce the mortality and morbidity. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3985363/ /pubmed/24741255 http://dx.doi.org/10.4103/0976-3147.127877 Text en Copyright: © Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Banakar, Basavaraj F. Pujar, Guruprasad S. Bhargava, Amita Khichar, Shubhkaran Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title | Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title_full | Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title_fullStr | Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title_full_unstemmed | Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title_short | Guillain-Barre syndrome with posterior reversible encephalopathy syndrome |
title_sort | guillain-barre syndrome with posterior reversible encephalopathy syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985363/ https://www.ncbi.nlm.nih.gov/pubmed/24741255 http://dx.doi.org/10.4103/0976-3147.127877 |
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