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Neuroleptic malignant syndrome due to risperidone misdiagnosed as status epilepticus
Ali Ertug Arslankoylu1, Meryem Ozlem Kutuk, Cetin Okuyaz
1Mersin University Faculty of Medicine, Department of Pediatrics, Pediatric Intensive Care Unit, Mersin, Turkey.
Abstract:
Neuroleptic malignant syndrome (NMS) is a rare but potentially fatal disease characterized by fever, muscle rigidity, delirium and autonomic instability. Here we report a child, with NMS due to the risperidone misdiagnosed as status epilepticus. Nine year old boy, who had been under high dose risperidone treatment for 8 weeks, admitted to the emergency room because of the contractions (evaluated as status epilepticus) persisting for 7 hours. Since there was neuroleptic treatment in the past medical history and, unconsciousness, muscular rigidity, diaphoresis, hypertermi and, hypotension in physical examination, leucocytosis and elevated creatininphosphokinase levels in laboratory tests, the patient was evaluated as NMS and discharged without any complications. We reported this case to point out that; NMS may be misdiagnosed as status epilepticus in children when EEG monitoring is unavailable. When a child admitted to the emergency room because of suspicious convulsion neuroleptic drug use must surely be asked.
Insights
Neuroleptic malignant syndrome (NMS), a rare but serious condition, can be mistaken for status epilepticus in children. Early recognition of NMS in pediatric patients is crucial for timely and appropriate treatment.
Area of Science:
- Pediatric Neurology
- Pharmacology
Background:
- Neuroleptic malignant syndrome (NMS) is a rare, life-threatening condition associated with antipsychotic medications.
- Risperidone is an antipsychotic medication sometimes used in pediatric patients.
Observation:
- A 9-year-old boy on high-dose risperidone presented with prolonged seizures, initially diagnosed as status epilepticus.
- Physical examination revealed rigidity, diaphoresis, hyperthermia, and hypotension, with laboratory findings of leucocytosis and elevated creatine phosphokinase.
- The patient's symptoms were ultimately attributed to NMS, not status epilepticus.
Findings:
- NMS can mimic status epilepticus in children, particularly when electroencephalogram (EEG) monitoring is unavailable.
- Prompt identification of NMS is critical, especially in patients with a history of neuroleptic medication use.
Implications:
- This case highlights the importance of considering NMS in the differential diagnosis of pediatric seizures, especially in patients with risk factors.
- Clinicians should inquire about neuroleptic medication use in children presenting with unexplained seizures or altered consciousness.
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