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Case Reports
. 2025 Jun 1;17(6):e85172.
doi: 10.7759/cureus.85172. eCollection 2025 Jun.

Hyperreflexia and Preserved Reflexes in Pediatric Guillain-Barré Syndrome: A Case Report and Literature Review

Affiliations
Case Reports

Hyperreflexia and Preserved Reflexes in Pediatric Guillain-Barré Syndrome: A Case Report and Literature Review

Shahd Abuhalima et al. Cureus. .

Abstract

Guillain-Barré syndrome (GBS) is the most prevalent cause of acute flaccid paralysis, often following an antecedent illness such as upper respiratory infections. Acute motor axonal neuropathy (AMAN), a subtype of GBS, predominantly affects motor axons, resulting in significant motor impairment, and is frequently associated with Campylobacter jejuni infection. We present a case of a three-year-old female patient who developed AMAN, a subtype of Guillain-Barré Syndrome (GBS). Approximately 10 days prior to admission, she had a history of fever, sore throat, and cough, which slightly improved for one day following a five-day course of antibiotics. However, her condition then worsened, and she began experiencing vomiting of gastric contents and occasional sputum production. Despite initial improvement, her condition deteriorated, leading to decreased muscle strength, exaggerated reflexes, and progressive respiratory failure. Neurophysiological studies, including nerve conduction studies (NCSs) and imaging, were consistent with AMAN. The patient was treated with intravenous immunoglobulin (IVIG) therapy and required endotracheal intubation for respiratory support. Over the course of her hospitalization, her neurological status improved significantly, and by day 9, she was able to walk with assistance, marking a successful recovery. This case highlights the importance of early diagnosis and intervention in managing GBS in pediatric patients, particularly in the context of atypical presentations, including hyperreflexia.

Keywords: acute motor axonal neuropathy; aman; atypical presentation; guillain-barré syndrome; hyperreflexia.

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Conflict of interest statement

Human subjects: Consent for treatment and open access publication was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Figures

Figure 1
Figure 1. Brain MRI of the patient on admission
Axial FLAIR brain MRI showing multiple nonspecific periventricular white matter hyperintense foci (red arrows). No diffusion restriction or abnormal enhancement is seen. The absence of central nervous system lesions helps exclude differential diagnoses such as ADEM, supporting a peripheral etiology consistent with the AMAN subtype of GBS. FLAIR: fluid-attenuated inversion recovery, MRI: magnetic resonance imaging, ADEM: acute disseminated encephalomyelitis, AMAN: acute motor axonal neuropathy, GBS: Guillain-Barré syndrome
Figure 2
Figure 2. Spinal MRI of the patient on admission
T1-weighted MRI of the lumbar spine demonstrating smooth thickening and enhancement of spinal nerve roots within the cauda equina and conus medullaris region (red arrows) in sagittal view, findings consistent with Guillain-Barré syndrome. MRI: magnetic resonance imaging

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