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Mushroom Poisoning

Mushroom poisoning results from ingestion of wild fungi that contain toxins, most often by foraging errors, and is seasonal (late summer and autumn in temperate regions). The key point is the time between eating and the first symptoms, which separates mostly benign early-onset syndromes (under 6 hours) from dangerous late-onset syndromes (over 6 hours).

Principal syndromes

  • Amatoxin (Amanita phalloides, Amanita virosa, Galerina and some Lepiota species): the cause of about 90% of fatal mushroom poisonings. Amatoxins inhibit RNA polymerase II and are concentrated by the liver through enterohepatic recirculation. A single cap (about 30 g) of death cap can be fatal. Without treatment, mortality is 10 to 30%.
  • Orellanine (Cortinarius orellanus and C. rubellus): delayed acute kidney injury 2 to 20 days after ingestion.
  • Gyromitrin (false morel, Gyromitra esculenta): metabolized to monomethylhydrazine, which depletes pyridoxal phosphate and causes seizures, hemolysis and hepatic injury.
  • Muscarine (Clitocybe and Inocybe species): cholinergic syndrome within 15 to 30 minutes.
  • Isoxazoles (Amanita muscaria, Amanita pantherina): ibotenic acid and muscimol cause confusion, ataxia and sedation.
  • Psilocybin (Psilocybe species): hallucinations.
  • Coprine (Coprinopsis atramentaria): a disulfiram-like reaction with alcohol.
  • Gastrointestinal irritants: many species cause self-limiting vomiting and diarrhea.

Amatoxin poisoning evolves in three phases: a latent phase of 6 to 24 hours, a gastrointestinal phase of profuse vomiting and cholera-like diarrhea (6 to 24 hours), a false recovery at 24 to 48 hours, and then hepatic and renal failure at 48 to 96 hours. Complications: fulminant liver failure, hepatic encephalopathy, coagulopathy, acute kidney injury, cerebral edema and death.

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