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Published on: July 8, 2025
[Patient with encephalitis presenting with olanzapine-responsive malignant catatonia]
Hayato Suzuki1, Takao Fukushima, Kunihiko Makino
1Department of Neurology, Shibata Hospital-Niigata Preferctural Hospital.
Abstract:
We report the case of a 29-year-old man, who could not remember some words of Kanji and showed emotional instability. Magnetic resonance imaging (MRI) scan of his brain appeared normal. Cerebrospinal fluid (CSF) analysis showed lymphocytic pleocytosis. An electroencephalogram (EEG) showed slow activities in both frontal regions of the brain. He was diagnosed as acute encephalitis. On his fourth hospital day, he was found to be catatonic and showed mutism, akinetism, and catalepsy. On the ninth day, he showed hyperpyrexia, muscle rigidity, difficulty in swallowing, respiratory insufficiency, and rhabdomyolysis (creatine phosphokinase (CK), 3038 IU/l). He was diagnosed as malignant catatonia. Intravenous administration of acyclovir, high-dose methylprednisolone, antibiotics, diazepam, and dantrolene sodium was not effective. After initiating oral administration of olanzapine, his condition improved.
Insights
A young man with acute encephalitis developed malignant catatonia, a rare neurological condition. Oral olanzapine effectively treated his severe symptoms, including mutism and muscle rigidity.
Area of Science:
- Neurology
- Neuroscience
- Critical Care Medicine
Background:
- Acute encephalitis can present with diverse neurological symptoms.
- Malignant catatonia is a severe, life-threatening syndrome characterized by motor disturbances, autonomic instability, and altered consciousness.
Observation:
- A 29-year-old man initially presented with memory deficits and emotional instability, diagnosed as acute encephalitis.
- His condition progressed to malignant catatonia, exhibiting mutism, akinetism, catalepsy, hyperpyrexia, muscle rigidity, dysphagia, respiratory insufficiency, and rhabdomyolysis.
- Cerebrospinal fluid analysis revealed lymphocytic pleocytosis, and electroencephalogram showed frontal slow activities.
Findings:
- Standard treatments for encephalitis and catatonia, including acyclovir, methylprednisolone, antibiotics, diazepam, and dantrolene sodium, were ineffective.
- The patient showed significant clinical improvement after initiating oral olanzapine.
- Magnetic resonance imaging (MRI) of the brain was normal despite severe neurological symptoms.
Implications:
- This case highlights the potential efficacy of olanzapine in managing malignant catatonia, even in refractory cases.
- It underscores the importance of considering malignant catatonia in the differential diagnosis of severe neurological deterioration following encephalitis.
- Further research is warranted to elucidate the neurobiological mechanisms underlying olanzapine's therapeutic effect in malignant catatonia.
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