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Acute cerebellar ataxia after influenza vaccination with recurrence and marked cerebellar atrophy
1Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, Sendai, Japan.
Insights
A child developed acute cerebellar ataxia after an influenza vaccine, experiencing recurrence and severe cerebellar atrophy. This case highlights a rare, persistent neurological outcome following vaccination.
Area of Science:
- Neurology
- Immunology
- Pediatrics
Background:
- Acute cerebellar ataxia (ACA) is a neurological disorder characterized by sudden onset of ataxia.
- Vaccinations, including influenza vaccines, are generally safe but can rarely be associated with neurological adverse events.
- Understanding the link between vaccinations and neurological conditions is crucial for public health and patient safety.
Observation:
- A previously healthy 5-year-old girl presented with ACA 8 days post-influenza vaccination.
- Cerebrospinal fluid (CSF) showed moderate pleocytosis, while initial brain CT was normal.
- Symptoms initially improved but recurred 33 months later, leading to persistent ataxia.
Findings:
- The patient developed marked cerebellar atrophy on CT and MRI 16 months after ataxia recurrence.
- This case represents the first documented instance of ACA with recurrence and severe cerebellar atrophy following vaccination.
- Etiology and pathogenesis of this rare neurological sequela remain undetermined.
Implications:
- This case underscores the importance of continued surveillance for rare neurological adverse events post-vaccination.
- Further research is needed to elucidate the mechanisms underlying vaccine-associated neurological complications.
- Long-term follow-up is essential for patients presenting with post-vaccination neurological syndromes.
Abstract:
A 5-year-old, previously healthy girl developed symptoms and signs of acute cerebellar ataxia (ACA) 8 days after having received an influenza vaccination. Brain CT was normal, but the CSF showed moderate pleocytosis. Symptoms almost disappeared within 4 months. Thirty-three months later, cerebellar symptoms recurred without apparent preceding episode, and persisted. Sixteen months after the recurrence of ataxia, CT and MRI revealed marked cerebellar atrophy. No further augmentation of ataxia or of cerebellar atrophy was observed during following 30 months. The patient appears to be the first documented case of ACA with recurrence of ataxia and severe atrophy of the cerebellum, though the etiology and pathogenesis are still to be determined. Clinical pictures and the course of the patient were compared with follow-up data on 8 cases of ACA.
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