• New Submission
  • Register
  • Login

International Clinical Neuroscience Journal

  • Home
  • About
    • About the Journal
    • Aim & Scope
    • Editorial Team
    • Peer Review Process
    • Journal Policies
    • Contact
  • For Authors
    • New Submission
    • Author Guidelines
    • ORCiD
    • Frequently Asked Questions (FAQ)
  • For Reviewers
    • Reviewers Guidelines
    • Responsibility of Reviewers
  • Issues
    • Current Issue
    • Archive
  • Indexing/Abstracting
  • Ethics
    • Ethical Requirements
    • Publication Ethics and Malpractice Statement
    • Article Withdrawal
    • Authorship Conflicts
    • Copyright Notice
    • Privacy Statement
    • Plagiarism Policy
    • CrossMark Policy
    • Advertising Policy
Advanced Search
  1. Home
  2. Archives
  3. Vol. 4 No. 2 (2017): Spring
  4. Case Report

Vol. 4 No. 2 (2017)

June 2017

A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis

  • Sadegh Izadi
  • Mehdi Karimian

International Clinical Neuroscience Journal, Vol. 4 No. 2 (2017), 12 June 2017 , Page 77-78
https://doi.org/10.22037/icnj.v4i2.16187 Published: 2017-06-12

  • View Article
  • Download
  • Cite
  • References
  • Statastics
  • Share

Abstract

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.

Keywords:
  • Guillain-Barre syndrome
  • lymphocytosis
  • cerebrospinal fluid
  • PDF

How to Cite

1.
Izadi S, Karimian M. A Case of Guillain-Barre Syndrome with Significant Lymphocytic Pleocytosis. Int Clin Neurosci J [Internet]. 2017 Jun. 12 [cited 2026 Jul. 5];4(2):77-8. Available from: https://journals.sbmu.ac.ir/neuroscience/article/view/16187
  • ACM
  • ACS
  • APA
  • ABNT
  • Chicago
  • Harvard
  • IEEE
  • MLA
  • Turabian
  • Vancouver
  • Endnote/Zotero/Mendeley (RIS)
  • BibTeX

References

Brettschneider J, Petzold A, Süssmuth S, Tumani H. Cerebrospinal fluid biomarkers in Guillain-Barrésyndrome-where do we stand? J Neurol. 2009 Jan; 256(1):3-12.

Gupta D, Nair M, Baheti NN, Sarma PS, Kuruvilla A. Electrodiagnostic and clinical aspects of Guillain-Barré syndrome: an analysis of 142 cases. J Clin Neuromuscul Dis. 2008 Dec; 10(2):42-51.

Uncini A, Yuki N. Electrophysiologic and immunopathologic correlates in Guillain-Barré syndrome subtypes. Expert Rev Neurother. 2009 Jun; 9(6):869-84.

Uncini A, Kuwabara S. Electrodiagnostic criteria for Guillain-Barrè syndrome: a critical revision and the need for an update. Clin Neurophysiol. 2012 Aug; 123(8):1487-95.

Akbayram S, Doğan M, Akgün C, Peker E, Sayιn R, Aktar F, and et al. Clinicalfeatures and prognosis with Guillain-Barré syndrome. Ann Indian Acad Neurol. 2011 Apr; 14(2):98-102.

Asbury AK. New concepts of Guillain-Barré syndrome. J Child Neurol. 2000 Mar; 15(3):183-91.

Rauschka H, Jellinger K, Lassmann H, Braier F, Schmidbauer M. Guillain-Barré syndrome with marked pleocytosis or a significant proportion of polymorphonuclear granulocytes in the cerebrospinal fluid: neuropathological investigation of five cases and review of differential diagnoses. Eur J Neurol. 2003 Sep; 10(5):479-86.

  • Abstract Viewed: 615 times
  • PDF Downloaded: 1350 times

Download Statastics

  • Linkedin
  • Twitter
  • Facebook
  • Google Plus
  • Telegram
  • Home
  • Archives
  • Submissions
  • About the Journal
  • Editorial Team
  • Contact

 

This journal is distributed under the terms of CC BY-NC 4.0. All credits and honors to PKP for their OJS. 

Support Contact: icnj.journal@gmail.com

 

Powered by OJSPlus