A Rare Case of Bickerstaff Encephalitis in Childhood: A Case Report

<b>Background:</b> Bickerstaff brainstem encephalitis (BBE) is a rare autoimmune disease and approximately 74 cases have been reported in the literature, mostly in childhood. <b>Methods:</b> We reported this case report according to the CARE guidelines. <b>Results:</b> A 13-year-old female presented with a 4-day history of persistent fever and hallucinations. She rapidly developed nystagmus associated with blurred vision with ataxic gait. She also developed altered mental status, blepharoptosis, diplopia and extrinsic ocular motility. An EEG showed asymmetric brain electrical activity with slow and spiky abnormalities in the left cerebral hemisphere. Lumbar puncture showed mild pleocytosis with lymphocytic predominance, elevated protein, with normal glucose. Anti-GM1 and anti-GM2 antibodies were positive. She was administered intravenous immunoglobulin therapy due to a suspicion of BBE, showing rapid improvement in mental status. <b>Conclusions:</b> BBE is a diagnosis of exclusion and should be considered especially in pediatric age.

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Journal
Neurology International
Published
2025-02-07
DOI
https://doi.org/10.3390/neurolint17020024
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
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article

A Rare Case of Bickerstaff Encephalitis in Childhood: A Case Report

Giuseppe Pulito, Pasquale Sansone, Luca Gregorio Giaccari, Luciana Mascia et al.
Neurology International
Peripheral Neuropathies and Disorders
article

A Rare Case of Bickerstaff Encephalitis in Childhood: A Case Report

Giuseppe Pulito, Pasquale Sansone, Luca Gregorio Giaccari, Luciana Mascia, Maria Caterina Pace, Rosella Barbieri, Gianfranco Paiano, Donatella Mastria, Rossella De Maglio, Francesca Madaro
article en

Abstract

<b>Background:</b> Bickerstaff brainstem encephalitis (BBE) is a rare autoimmune disease and approximately 74 cases have been reported in the literature, mostly in childhood. <b>Methods:</b> We reported this case report according to the CARE guidelines. <b>Results:</b> A 13-year-old female presented with a 4-day history of persistent fever and hallucinations. She rapidly developed nystagmus associated with blurred vision with ataxic gait. She also developed altered mental status, blepharoptosis, diplopia and extrinsic ocular motility. An EEG showed asymmetric brain electrical activity with slow and spiky abnormalities in the left cerebral hemisphere. Lumbar puncture showed mild pleocytosis with lymphocytic predominance, elevated protein, with normal glucose. Anti-GM1 and anti-GM2 antibodies were positive. She was administered intravenous immunoglobulin therapy due to a suspicion of BBE, showing rapid improvement in mental status. <b>Conclusions:</b> BBE is a diagnosis of exclusion and should be considered especially in pediatric age.

Neurology InternationalVol. 17(2)
University of Salento (IT), University of Campania "Luigi Vanvitelli" (IT), Ospedale Vito Fazzi (IT)
Reduced inequalities
Openalex Percentile: Top 96%
Peripheral Neuropathies and Disorders
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A Rare Case of Bickerstaff Encephalitis in Childhood: A Case Report — Giuseppe Pulito, Pasquale Sansone, et al. · Neurology International (2025) | TGRS Research Map | TGRS