A Case Report: Rare Presentation of Intracranial Hemorrhage post Guillain Barré Syndrome
DOI:
https://doi.org/10.38179/ijcr.v1i1.23Keywords:
Guillain Barre Syndrome, Intracranial Hemorrhage, IVIG, cerebral vasospasm, case reportAbstract
Background: Guillain Barre Syndrome (GBS) is an autoimmune disease where antibodies attack the myelin sheath of peripheral nerves. The hallmark of the disease includes symmetrical quadriparesis, respiratory distress, and failure with subsequent need for mechanical ventilation. Most cases occur after a viral or bacterial infection. Other causes, such as intracranial hemorrhage, also exist, and several case studies report an association between these two pathologies.
Case Report: In this report, we present the case of an elderly male patient with intracranial (IC) bleeding post-GBS. The patient was admitted to the hospital for dyspnea and diagnosed with pneumonia. When he started complaining of progressive bilateral ascending paralysis of his lower extremities, we performed a lumbar puncture, and he was diagnosed with GBS. We started him on intravenous immune globulins (IVIGs) immediately, but his weakness progressed to include his respiratory muscles, and he required mechanical ventilatory support with Intensive Care Unit (ICU) admission. We extubated him after two weeks, but he needed to be reintubated 24 hours later for a severely decreased level of consciousness. An urgent computed tomography scan of the brain showed IC bleeding. The patient developed a septic shock due to his pneumonia, which was refractory to antibiotics and vasopressors. He passed away a few weeks after that.
Conclusion: Our case represents a unique type of association between IC hemorrhages and GBS, where the bleeding occurred several days after, as opposed to before GBS. It also reinforces the correlation between GBS and Intracranial bleeding and stresses the importance of having a high index of suspicion when facing either pathology since both have similar symptoms that may overlap or mask each other.
References
Nguyen TP, Taylor RS. Guillain Barre Syndrome. 2020 Jul 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. PMID: 30335287.
Pritchard J. Guillain-Barré syndrome. Clin Med (Lond). 2010 Aug;10(4):399-401. doi: 10.7861/clinmedicine.10-4-399. PMID: 20849020; PMCID: PMC4952175. https://doi.org/10.7861/clinmedicine.10-4-399
Winer JB. An update in guillain-barré syndrome. Autoimmune Dis. 2014;2014:793024. doi: 10.1155/2014/793024. Epub 2014 Jan 6. PMID: 24511391; PMCID: PMC3910670. https://doi.org/10.1155/2014/793024
Sudulagunta SR, Sodalagunta MB, Sepehrar M, Khorram H, Bangalore Raja SK, Kothandapani S, Noroozpour Z, Aheta Sham M, Prasad N, Sunny SP, Mohammed MD, Gangadharappa R, Nidsale Sudarshan R. Guillain-Barré syndrome: clinical profile and management. Ger Med Sci. 2015 Sep 21;13:Doc16. doi: 10.3205/000220. PMID: 26421004; PMCID: PMC4576316. https://doi.org/10.1093/omcr/omv054
Zhao PP, Ji QK, Sui RB, Zhang R, Zhang LJ, Xu ZX, Li Q, Ji SB, Zhao JH. Increased intracranial pressure in Guillain-Barré syndrome: A case report. Medicine (Baltimore). 2018 Jul;97(30):e11584. doi: 10.1097/MD.0000000000011584. PMID: 30045288; PMCID: PMC6078745. https://doi.org/10.1097/MD.0000000000011584
Joshi S, Musuka TD. Guillain-Barré syndrome as a complication of hypertensive basal ganglia haemorrhage. J Clin Neurosci. 2019 Jun;64:54-56. doi: 10.1016/j.jocn.2019.02.018. Epub 2019 Mar 6. PMID: 30852075. https://doi.org/10.1016/j.jocn.2019.02.018
Wu Q, Liu N, Pan C, Bu B, Tang Z. Guillain-Barré Syndrome and Cerebral Hemorrhage: Two Cases and Literature Review. Eur Neurol. 2016;76(3-4):182-186. doi: 10.1159/000450603. Epub 2016 Sep 27. PMID: 27669485. https://doi.org/10.1159/000450603
Jia H, Tian Y, Wu YM, Li B. Two cases of Guillain-Barré syndrome after cerebral hemorrhage or head trauma. NeuroimmunolNeuroinflamm. 2017;4(61-4). https://doi.org/10.20517/2347-8659.2016.51
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