Recurrence of Guillain-Barre syndrome: a case report

Authors

DOI:

https://doi.org/10.26871/killcanasalud.v8i3.1607

Keywords:

Guillain-Barré syndrome, polyneuropathies, recurrence, muscle weakness, immunoglobulin

Abstract

Introduction: Guillain-Barré syndrome (GBS) is an acute immune-mediated polyneuropathy preceded by infections in up to 60% of cases. The incidence of GBS is 1-2 cases per 100,000 people per year, with a 20% increase with each decade of age. The recurrence rate is estimated at 5%, making it a rare event. Analysis: The patient presented with initial symptoms suggestive of a respiratory infection, but progression to paresthesias and severe limb weakness, along with areflexia, raised suspicion of recurrent GBS. The diagnosis was confirmed clinically using the Brighton criteria, supported by neurophysiological studies. The severity (GBS-DS 3) warranted urgent hospital admission. Case Outcome: The patient was treated with intravenous immunoglobulin (IVIG) at a dose of 0.4 g/kg/day for 3 days, along with analgesics for neuropathic pain and early physical therapy. The patient was subsequently discharged to an outpatient rehabilitation program. At 3 months of follow-up, the patient achieved complete remission, similar to his first episode. Discussion: This case highlights the rarity of GBS recurrence and its association with respiratory infections. Although the absence of a lumbar puncture limits complete diagnostic confirmation, neurophysiological studies and treatment response support the diagnosis. The choice of IVIG was appropriate according to current guidelines, and clinical improvement without the use of corticosteroids reinforces the evidence that these are not recommended for GBS.

Downloads

Download data is not yet available.

References

Yuki N, Hartung HP. Guillain-Barré syndrome. N Engl J Med. 2012;366(24): 2294-2304. Available in: https://www.nejm.org/doi/abs/10.1056/NEJMra1114525

Shahrizaila N, Lehmann HC, Kuwabara S. Guillain-Barré syndrome. Lancet. 2021; 397(10280):1214-1228. Available in: https://pubmed.ncbi.nlm.nih.gov/33647239/

Krishna D, Chakrabarty B. The Curious Story of Recurrent Guillain-Barré Syndrome; A Lot More to Know. Indian J Pediatr. 2024 May;91(5):428-429. DOI: https://doi.org/10.1007/s12098-024-05031-2

Imam K, Liu A. A case of Recurrent Guillain-Barre Syndrome observed by the same clinician 12 years apart. Clin Case Rep. 2020 Jun;8(8):1376-1378. Available in: https://pmc.ncbi.nlm.nih.gov/articles/PMC7455452/

Domínguez CLG, Alcocer MJL, Domínguez GLG, Arellano AJG. Síndrome de Guillain-Barré recurrente asociado con infección por SARS-CoV-2. Acta Med GA. 2021; 19 (4): 554-557. DOI: https://dx.doi.org/10.35366/102546

Kuitwaard K, van Koningsveld R, Ruts L, Jacobs BC, van Doorn PA. Recurrent Guillain-Barré syndrome. J Neurol Neurosurg Psychiatry. 2009 Jan;80(1):56-59. Available in: https://jnnp.bmj.com/content/jnnp/80/1/56.full.pdf

Expósito J, Carrera L, Natera D, Nolasco G, Nascimiento A, Ortez C. Síndrome de Guillain-Barré y otras neuropatías autoinmunes: tratamiento actual. Medicina. 2022; 82 Suppl 3: 82-88. Disponible en: https://www.medicinabuenosaires.com/revistas/vol82-22/s3/82s3.pdf

Walling AD, Dickson G. Guillain-Barré syndrome. Am Fam Physician. 2013 Feb 1;87(3):191-7. PMID: 23418763. Disponible en: https://pubmed.ncbi.nlm.nih.gov/23418763/

Van Doorn PA, Van Den Bergh PYK, Hadden RDM, Avau B, Vankrunkelsven P, Attarian S, et al. European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillan-Barré syndrome. Eur J Neurol. 2023 Dec;30(12):3646-3674. DOI: https://doi.org/10.1111/ene.16073

Newswanger DL, Warren CR. Guillain-Barré syndrome. Am Fam Physician. 2004 May 15;69(10):2405-10. PMID: 15168961. Disponible en: https://pubmed.ncbi.nlm.nih.gov/15168961/

McDonnell EP, Altomare NJ, Parekh YH, Gowda RC, Parikh PD, Lazar MH, Blaser MJ. COVID-19 as a Trigger of Recurrent Guillain-Barré Syndrome. Pathogens. 2020 Nov;9(11):965. DOI: https://doi.org/10.3390/pathogens9110965

Alva-Diaz C, Mori N, Pacheco-Barrios K, Velásquez-Rimachi V, Rivera-Torrejon O, Huerta-Rosario CA, et al. Guía de práctica clínica para el diagnóstico y tratamiento del paciente con síndrome de Guillain-Barré. Neurol Argent. 2020;12(1):36–48. DOI: https://doi.org/10.1016/j.neuarg.2019.09.006

Bellanti R, Rinaldi S. Guillain-Barré syndrome: a comprehensive review. Eur J Neurol. 2024 Aug;31(8):e16365. DOI: https://doi.org/10.1111/ene.16365

Dimachkie MM, Barohn RJ. Guillain-Barré syndrome and variants. Neurol Clin. 2013 May;31(2):491-510. DOI: https://doi.org/10.1016/j.ncl.2013.01.005

Malek E, Salameh J. Guillain-Barre Syndrome. Semin Neurol. 2019 Oct;39(5):589-595. DOI: https://doi.org/10.1055/s-0039-1693005

Mirian A, Nicolle MW, Budhram A. Guillain-Barré syndrome. CMAJ. 2021 Mar;193(11):E378. DOI: https://doi.org/10.1503/cmaj.202710

Gunatilake SSC, Gamlath R, Wimalaratna H. An unusual case of recurrent Guillain-Barré syndrome with normal cerebrospinal fluid protein levels: a case report. BMC Neurol [Internet]. 2016;16(1):161. Disponible en: http://dx.doi.org/10.1186/s12883-016-0687-z

Verboon C, van Doorn PA, Jacobs BC. Treatment dilemmas in Guillain-Barré syndrome. J Neurol Neurosurg Psychiatry. 2017 Apr; 88(4): 346-352. DOI: https://doi.org/10.1136/jnnp-2016-314862

Yao J, Zhou R, Liu Y, Lu Z. Progress in Guillain-Barré syndrome immunotherapy-A narrative review of new strategies in recent years. Hum Vaccin Immunother. 2023 Aug;19(2):2215153. DOI: https://doi.org/10.1080/21645515.2023.2215153

Liu S, Dong C, Ubogu EE. Immunotherapy of Guillain-Barré syndrome. Hum Vaccin Immunother. 2018;14(11):2568-2579. DOI: https://doi.org/10.1080/21645515.2018.1493415

Querol L, Lleixà C. Novel Immunological and Therapeutic Insights in Guillain-Barré Syndrome and CIDP. Neurotherapeutics. 2021 Oct;18(4):2222-2235. DOI: https://doi.org/10.1007/s13311-021-01117-3

Published

2024-12-05
ESTADISTICAS
  • Abstract 0
  • PDF (Español (España)) 0

How to Cite

Martínez Borrero, P., & Machado Tello, M. D. (2024). Recurrence of Guillain-Barre syndrome: a case report. Killkana Salud Y Bienestar, 8(3), 73–82. https://doi.org/10.26871/killcanasalud.v8i3.1607