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Coma and confirmed epileptiform activity induced by Amanita pantherina poisoning.

Marco Cirronis, A. Giampreti, G. Eleftheriou, Mariapina Gallo, Gioia Contessa, L. Faraoni, R. Butera, G. Bacis

Toxicon December 1, 2024 DOI: 10.1016/j.toxicon.2024.108208 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Case study Case report Peer reviewed
Sample size 1
Population A 56-year-old woman who ingested Amanita pantherina mushrooms
Interventions Gastrointestinal decontamination Levetiracetam
Dose Levetiracetam 3.000 mg/day
Duration Levetiracetam stopped after two months; clonic movements and agitation up to the 7th day of hospitalization
Measures Electroencephalogram, unenhanced brain CT, cerebral CT angiography, toxicological screening
Key findings The authors report that a 56-year-old woman developed severe coma and seizures after eating Amanita pantherina picked in her garden, with epileptiform activity on EEG and clonic movements persisting to day 7 of hospitalization. She recovered without sequelae after gastrointestinal decontamination and levetiracetam (3,000 mg/day, stopped after two months). The authors argue that mushroom ingestion should be considered in the diagnostic workup of unexplained coma and convulsions.

Abstract

Amanita pantherina poisoning is a rare event poorly described. The clinical picture is usually associated with the one of A. muscaria, but A. pantherina contains more muscimol causing more often coma. We describe a case of severe coma and seizures after A. pantherina ingestion. A woman of 56 years old was found at home unresponsive with miosis, clonic movements of four limbs, normal respiratory and cardiovascular functions and without cerebral ischemic symptoms. Her husband reported mushrooms ingestion 4 hours earlier that were picked up in the home garden and believed to be Macrolepiota procera. Unenhanced brain CT and cerebral CT angiography were normal. Blood tests were within normal range, including troponin I, creatine phosphokinase and lactate. Toxicological screening was negative for methadone, ecstasy, amphetamines, barbiturate, cannabinoids, cocaine, opioids and benzodiazepines. Suspecting ingestion of A. pantherina, gastrointestinal decontamination was done. Mycological examination of residual stems of the ingested mushrooms identified A. pantherina, and evaluation of photos of the same mushrooms growing in their garden confirmed the species. Electroencephalogram confirmed epileptiform activity and levetiracetam 3.000 mg/day was started. The patient was always hemodynamically stable but daily neurologic wake-up test highlighted the presence of agitation and clonic movements of the limbs up to the 7th day of hospitalization. Levetiracetam was tapered and stopped after two months based on neurological improvement. The patient recovered without sequelae. Amanita pantherina poisoning is a rare event and clinical picture of convulsions and coma often guides the diagnosis towards organic pathologies. The latter should be excluded first but an accurate anamnesis should also consider mushrooms consumption. Gastrointestinal decontamination may be the only therapy for reducing toxins absorption and clinical severity. Our patient had acute severe neurological effects lasted many days, but she completely recovered with intensive treatment and levetiracetam administration.

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