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A Complex Presentation: Psychosis in a Patient Diagnosed With Lennox-Gastaut Syndrome
Gurraj Singh1, Gurtej Gill2, Satwant Singh3
1Psychiatry, Bergen New Bridge Medical Center, Paramus, USA.
Insights
Lennox-Gastaut syndrome (LGS) is a severe epilepsy. This case study details a 19-year-old male with LGS experiencing challenging seizures, cognitive decline, and rare psychotic symptoms.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Clinical Case Study
Background:
- Lennox-Gastaut syndrome (LGS) is a severe, treatment-resistant epilepsy in children.
- It often presents with multiple seizure types and leads to cognitive impairment and intellectual disability.
- Management is complex due to comorbidities and refractory seizures.
Abstract:
Lennox-Gastaut syndrome (LGS) is a form of severe childhood epilepsy, with most children experiencing seizures before reaching the age of eight. Typically, patients have multiple types of seizures, making an accurate diagnosis challenging. While it can be secondary to other causes, often, it is idiopathic. Over time, children develop cognitive impairment, leading to intellectual disability. The mainstay of treatment and management is seizure control. However, management remains challenging due to the complexity of the syndrome, as it is associated with multiple seizure types, intellectual deterioration, and other psychiatric comorbidities. We present the case of a 19-year-old male diagnosed with LGS and treated with various available therapies, who demonstrated multiple breakthrough seizures, significant neurocognitive disabilities, and behavior challenges. Additionally, the patient displayed psychotic features of auditory hallucinations, aggression, and attempts at self-mutilation, a rare clinical presentation in LGS.
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