Cargando…

A case of brucellosis-induced Guillain–Barre syndrome

BACKGROUND: Guillain–Barre syndrome (GBS) is a rare neurological complication of brucellosis, and neurobrucellosis is the most common, but they have many similarities in clinical manifestations. Many clinicians are accustomed to merely explaining the manifestations of nervous system involvement with...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Qian, Liu, Jianfeng, Jiang, Wenhui, Jiang, Lisheng, Lu, Mengzhi, Xiao, Linping, Li, Yukun, Lan, Yinghua, Li, Yongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781241/
https://www.ncbi.nlm.nih.gov/pubmed/35057735
http://dx.doi.org/10.1186/s12879-021-07025-3
_version_ 1784638041992724480
author Li, Qian
Liu, Jianfeng
Jiang, Wenhui
Jiang, Lisheng
Lu, Mengzhi
Xiao, Linping
Li, Yukun
Lan, Yinghua
Li, Yongguo
author_facet Li, Qian
Liu, Jianfeng
Jiang, Wenhui
Jiang, Lisheng
Lu, Mengzhi
Xiao, Linping
Li, Yukun
Lan, Yinghua
Li, Yongguo
author_sort Li, Qian
collection PubMed
description BACKGROUND: Guillain–Barre syndrome (GBS) is a rare neurological complication of brucellosis, and neurobrucellosis is the most common, but they have many similarities in clinical manifestations. Many clinicians are accustomed to merely explaining the manifestations of nervous system involvement with neurobrucellosis, but they ignore the possibility of GBS, and this leads to misdiagnosis, untimely treatment, and serious consequences. CASE PRESENTATION: A 55-year-old male patient was admitted to The First Affiliated Hospital of Harbin Medical University for intermittent fever, fatigue, and waist pain more than three months. Brucellosis was diagnosed from the blood test. Although anti-brucella treatment was given at the time of diagnosis, the disease continued to progress. At the time of the cerebrospinal fluid systematic physical examination and the neuroelectrophysiological test, acute motor sensory axonal neuropathy was diagnosed. The patient was given immediately administered immunoglobulin therapy. After three months of systemic treatment, the patient's muscle strength of the distal limbs gradually recovered. The numbness of the limbs eased slowly, and urination function and respiratory function returned to normal. He could sit by himself. CONCLUSIONS: The possibility of GBS should be closely monitored for when a brucellosis patient shows typical clinical manifestations of progressive muscle weakness, protein-cell separation of the cerebral spinal fluid, and typical demyelinating sensorimotor polyneuropathy.
format Online
Article
Text
id pubmed-8781241
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-87812412022-01-24 A case of brucellosis-induced Guillain–Barre syndrome Li, Qian Liu, Jianfeng Jiang, Wenhui Jiang, Lisheng Lu, Mengzhi Xiao, Linping Li, Yukun Lan, Yinghua Li, Yongguo BMC Infect Dis Case Report BACKGROUND: Guillain–Barre syndrome (GBS) is a rare neurological complication of brucellosis, and neurobrucellosis is the most common, but they have many similarities in clinical manifestations. Many clinicians are accustomed to merely explaining the manifestations of nervous system involvement with neurobrucellosis, but they ignore the possibility of GBS, and this leads to misdiagnosis, untimely treatment, and serious consequences. CASE PRESENTATION: A 55-year-old male patient was admitted to The First Affiliated Hospital of Harbin Medical University for intermittent fever, fatigue, and waist pain more than three months. Brucellosis was diagnosed from the blood test. Although anti-brucella treatment was given at the time of diagnosis, the disease continued to progress. At the time of the cerebrospinal fluid systematic physical examination and the neuroelectrophysiological test, acute motor sensory axonal neuropathy was diagnosed. The patient was given immediately administered immunoglobulin therapy. After three months of systemic treatment, the patient's muscle strength of the distal limbs gradually recovered. The numbness of the limbs eased slowly, and urination function and respiratory function returned to normal. He could sit by himself. CONCLUSIONS: The possibility of GBS should be closely monitored for when a brucellosis patient shows typical clinical manifestations of progressive muscle weakness, protein-cell separation of the cerebral spinal fluid, and typical demyelinating sensorimotor polyneuropathy. BioMed Central 2022-01-20 /pmc/articles/PMC8781241/ /pubmed/35057735 http://dx.doi.org/10.1186/s12879-021-07025-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Li, Qian
Liu, Jianfeng
Jiang, Wenhui
Jiang, Lisheng
Lu, Mengzhi
Xiao, Linping
Li, Yukun
Lan, Yinghua
Li, Yongguo
A case of brucellosis-induced Guillain–Barre syndrome
title A case of brucellosis-induced Guillain–Barre syndrome
title_full A case of brucellosis-induced Guillain–Barre syndrome
title_fullStr A case of brucellosis-induced Guillain–Barre syndrome
title_full_unstemmed A case of brucellosis-induced Guillain–Barre syndrome
title_short A case of brucellosis-induced Guillain–Barre syndrome
title_sort case of brucellosis-induced guillain–barre syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781241/
https://www.ncbi.nlm.nih.gov/pubmed/35057735
http://dx.doi.org/10.1186/s12879-021-07025-3
work_keys_str_mv AT liqian acaseofbrucellosisinducedguillainbarresyndrome
AT liujianfeng acaseofbrucellosisinducedguillainbarresyndrome
AT jiangwenhui acaseofbrucellosisinducedguillainbarresyndrome
AT jianglisheng acaseofbrucellosisinducedguillainbarresyndrome
AT lumengzhi acaseofbrucellosisinducedguillainbarresyndrome
AT xiaolinping acaseofbrucellosisinducedguillainbarresyndrome
AT liyukun acaseofbrucellosisinducedguillainbarresyndrome
AT lanyinghua acaseofbrucellosisinducedguillainbarresyndrome
AT liyongguo acaseofbrucellosisinducedguillainbarresyndrome
AT liqian caseofbrucellosisinducedguillainbarresyndrome
AT liujianfeng caseofbrucellosisinducedguillainbarresyndrome
AT jiangwenhui caseofbrucellosisinducedguillainbarresyndrome
AT jianglisheng caseofbrucellosisinducedguillainbarresyndrome
AT lumengzhi caseofbrucellosisinducedguillainbarresyndrome
AT xiaolinping caseofbrucellosisinducedguillainbarresyndrome
AT liyukun caseofbrucellosisinducedguillainbarresyndrome
AT lanyinghua caseofbrucellosisinducedguillainbarresyndrome
AT liyongguo caseofbrucellosisinducedguillainbarresyndrome