A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis
Guillain-Barre syndrome (GBS) is an immune-mediated polyneuropathy. In the cerebrospinal fluid (CSF) characteristic increased protein without pleocytosis i.e., albuminocytologic dissociation is seen. But cases of GBS with significant CSF lymphocytosis have rarely been reported. Here, we present a 38...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Shahid Beheshti University of Medical Sciences
2017-04-01
|
Series: | International Clinical Neuroscience Journal |
Online Access: | http://journals.sbmu.ac.ir/Neuroscience/article/download/16187/8 |
id |
doaj-fee19627c61e47abae47b8927f190441 |
---|---|
record_format |
Article |
spelling |
doaj-fee19627c61e47abae47b8927f1904412020-11-25T00:44:54ZengShahid Beheshti University of Medical SciencesInternational Clinical Neuroscience Journal2383-18712383-20962017-04-0142777810.22037/icnj.v4i2.16187icnj-3126A Case of Guillain-Barre Syndrome with Significant Lymphocytic PleocytosisSadegh Izadi0Mehdi Karimian1Clinical Neurology Research Center, Shiraz University of Medical Sciences, Shiraz IranResident of Neurology, Shiraz University of Medical Sciences, Shiraz IranGuillain-Barre syndrome (GBS) is an immune-mediated polyneuropathy. In the cerebrospinal fluid (CSF) characteristic increased protein without pleocytosis i.e., albuminocytologic dissociation is seen. But cases of GBS with significant CSF lymphocytosis have rarely been reported. Here, we present a 38-year-old man with dysarthria, dysphagia, bilateral facial palsy, and limb weakness with the diagnosis of GBS. Nerve Conduction Study confirmed the diagnosis but interestingly in the CSF study increased protein and lymphocytic predominant pleocytosis were found. Other possible differential diagnoses were ruled out by appropriate paraclinical studies. The patient underwent treatment with intravenous immunoglobulin and showed favorable response.http://journals.sbmu.ac.ir/Neuroscience/article/download/16187/8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sadegh Izadi Mehdi Karimian |
spellingShingle |
Sadegh Izadi Mehdi Karimian A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis International Clinical Neuroscience Journal |
author_facet |
Sadegh Izadi Mehdi Karimian |
author_sort |
Sadegh Izadi |
title |
A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis |
title_short |
A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis |
title_full |
A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis |
title_fullStr |
A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis |
title_full_unstemmed |
A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis |
title_sort |
case of guillain-barre syndrome with significant lymphocytic pleocytosis |
publisher |
Shahid Beheshti University of Medical Sciences |
series |
International Clinical Neuroscience Journal |
issn |
2383-1871 2383-2096 |
publishDate |
2017-04-01 |
description |
Guillain-Barre syndrome (GBS) is an immune-mediated polyneuropathy. In the cerebrospinal fluid (CSF) characteristic increased protein without pleocytosis i.e., albuminocytologic dissociation is seen. But cases of GBS with significant CSF lymphocytosis have rarely been reported. Here, we present a 38-year-old man with dysarthria, dysphagia, bilateral facial palsy, and limb weakness with the diagnosis of GBS. Nerve Conduction Study confirmed the diagnosis but interestingly in the CSF study increased protein and lymphocytic predominant pleocytosis were found. Other possible differential diagnoses were ruled out by appropriate paraclinical studies. The patient underwent treatment with intravenous immunoglobulin and showed favorable response. |
url |
http://journals.sbmu.ac.ir/Neuroscience/article/download/16187/8 |
work_keys_str_mv |
AT sadeghizadi acaseofguillainbarresyndromewithsignificantlymphocyticpleocytosis AT mehdikarimian acaseofguillainbarresyndromewithsignificantlymphocyticpleocytosis AT sadeghizadi caseofguillainbarresyndromewithsignificantlymphocyticpleocytosis AT mehdikarimian caseofguillainbarresyndromewithsignificantlymphocyticpleocytosis |
_version_ |
1725272527350005760 |