Abstract

Introduction: Botulinum neurotoxin A (BoNT-A) is widely used in various conditions that cause involuntary muscle contractions, such as management of spasticity in cerebral palsy (CP). However, iatrogenic botulism resulting from systemic effects from BoNT-A is uncommon but may have serious life-threatening consequences. Case Report: We report a case of pediatric patient who developed iatrogenic botulism after therapeutic intramuscular injections of BoNT-A. Conclusion: This case highlights the importance of clinicians having adequate information of the risk of systemic botulism following local injections of BoNT-A and caution is needed in using this therapy.

Highlights

  • Botulinum neurotoxin A (BoNT-A) is widely used in various conditions that cause involuntary muscle contractions, such as management of spasticity in cerebral palsy (CP)

  • Botulinum neurotoxins when injected locally into the muscle act at the neuromuscular junction resulting in dose-dependent muscle paralysis [3]

  • We describe a case of a child with CP who developed iatrogenic botulism after injections of therapeutic doses of botulinum toxin for lower limb spasticity

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Summary

INTRODUCTION

Paralytic illness produced by neurotoxin of Clostridium botulinum, an anaerobic, spore-forming bacterium [1]. Botulinum neurotoxins when injected locally into the muscle act at the neuromuscular junction resulting in dose-dependent muscle paralysis [3]. It causes reversible muscle weakness and inhibits acetylcholine release for about three months [5]. Details of the adverse effects and deaths following treatment with BoNT-A in children with CP are limited. We describe a case of a child with CP who developed iatrogenic botulism after injections of therapeutic doses of botulinum toxin for lower limb spasticity. A 5-year-old male child with CP presented with botulism-like manifestations 10 days after receiving multilevel injections, total dose of 500 units of BoNT-A (Dysport®) in his lower limbs to relieve muscle spasticity. The symptoms were gradually resolved on subsequent follow-up visits and completely recovered in two months

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