mushroom poisoning syndromes
There are many different types of mycotoxins. Of 14 distinctive types of mushroom poisoning found worldwide, so far about 10 distinctive patterns of reactions to mycotoxins have been observed in North America. However, since most mushroom species are rarely eaten, many toxins are poorly documented and syndromes not yet observed in North America may turn up as more and more peole experiment with eating wild mushrooms. NAMA maintains a case registry where you may report instances of mushroom poisoning.
The following list is not exhaustive. It is presented here for informational purposes, and should not be considered an aid to diagnosis. The images are shown as examples only and should not be used for identification. For emergency identification, please consult our list of volunteers. If you suspect that you have consumed a poisonous mushroom, contact a physician, or your local poison control center.
- Gastrointestinal Irritants
- Isoxazole Derivatives (Muscimol, Ibotenic Acid, and relatives)
- Amanitin (Amatoxins)
- Psilocybin, Psilocin, and other Indole Derivatives
- Corpine and other Alcohol Induced syndromes
- Allenic Norleucine and Delayed Kidney Damage
- Miscellaneous and Unknown Toxins
The most frequent form of mushroom poisoning is caused by a wide variety of gastrointestinal irritants. The symptoms usually appear within 20 minutes to 4 hours of ingesting the mushrooms, and include nausea, vomiting, cramps, and diarrhea, which normally pass after the irritant had been expelled. Severe cases may require hospitalization. Treatment is largely supportive - helping the patient's body to eliminate what it's not equipped to handle. Recovery is complete, though a bout with severe gastro-intestinal distress may put one off ever eating mushrooms again! IMPORTANT: If the gastrointestinal distress begins 6 to 24 hours after ingestion of the mushrooms, there is a possibility of a very serious toxicity from Amatoxins (see Amanitin). GI onset of 4-11 hours with impaired kidney function could be due to Allenic Norleucine (2-amino-4,5-hexadienoic acid). GI onset greater that 24 hours and up to 21 days could be due to Orellanine.
Mushrooms: Inocybe species, Clitocybe dealbata, and several relatives, Omphalatus species, and certain red-pored Boletus.
|Inocybe lanuginosa||Clitocybe dealbata||Omphalotus illudens||Boletus eastwoodiae|
The symptoms usually occur within 15-30 minutes of ingestion, and are focused on the involuntary nervous system. They include excessive salivation, sweating, tears, lactation (in pregnant women), plus severe vomiting and diarrhea. These symptoms may be accompanied by visual disturbances, irregular pulse, decreased blood pressure, and difficulty breathing. Victims normally recover within 24 hours, but severe cases may result in death due to respiratory failure. Atropine is a specific antidote, but must be administered by a physician. Dogs are particularly susceptible to the toxin muscarine.
Isoxazole Derivatives (Muscimol, Ibotenic Acid, and relatives)
Mushrooms: Amanita muscaria, A. pantherina, A. gemmata, Amanita multisquamosa (syn. A. cothurnata), A. frostiana, A. crenulata, A. strobiliformus, Tricholoma muscarium.
|Amanita muscaria||Amanita pantherina||Amanita gemmata||Amanita multisquamosa|
There is a great deal of confusion concerning these toxins, and much misinformation about their treatment. Atropine is NOT indicated in cases of poisoning by ibotenic acid or muscimol but is frequently cited as a treatment for A. muscaria poisonings in the medical literature, where the toxin is erroneously listed as muscarine! Atropine's effects are close to those of ibotenic acid, and may even exacerbate the symptoms.
Symptoms appear within 30 minute to 2 hours after ingestion, and last for several hours. Nausea and vomiting are quite common, but the principle effects are on the central nervous system: confusion, visual distortion, a feeling of greater strength, delusions and convulsions. Drowsiness is a common symptom, and many who ingest these mushrooms fall asleep and can not be roused. In rare cases the coma-like state can last for more than 24 hours. This facet of the syndrome can be particularly frightening for the attending physician, as most cases involve patients who arrive in this apparently comatose state. The resulting panicked reaction and overtreatment, generally produces no benefit to the patient. In humans, there are no reliably documented cases of death from toxins in these mushrooms in the past 100 years, though there is one case where a camper froze to death while in the comatose state. Dogs and especially cats can die from these isoxazole toxins, though it is important for the vet not to euthanize an animal even though the chances for recovery appear remote — once the animal awakens from the comatose state recovery is normally complete over the course of a week or so.
Treatment of humans and animals is largely supportive — reassuring the patient that the effects are only temporary. Recovery is normally spontaneous. To reiterate: Muscarine plays no documented clinical role in poisonings by Amanita muscaria or A. pantherina. Atropine is not indicated.
Mushrooms: Amanita phallodies, A. ocreata, A. verna, A. bisporigera, Conocybe filaris, Galerina autumnalis, G. marginata, G. venenata, Lepiotia castanea, L. helveola, L. subincarnata (=L. josserandii?) and close relatives.
|Amanita phalloides||Amanita ocreata||Conocybe filaris||Galerina autumnalis|
Extremely Serious. The fatality rate for Amanitin poisoning is about 50% without prompt, knowledgeable medical treatment, but is about 10% in the U.S. and Canada where good medical care is readily available. Amatoxins are doubly dangerous due to the fact that the symptoms are delayed for 6 to 24 hours after ingestion, by which time the toxins have been completely absorbed by the body and after the initial state of gastric distress, the patient appears to recover and is sometimes sent home. Monitoring of liver enzyme function is critical in cases of delayed onset GI distress!
Amanitins are a group of complex cyclic polypeptides which damage tissues by inhibiting RNA synthesis within each individual cell. Onset of symptoms manifests itself in four stages:
- First stage is a latency period of 6 to 24 hours after ingestion, in which the toxins are actively destroying the victim's kidneys and liver, but the victim experiences no discomfort.
- Second stage is a period of about 24 hours characterized by violent vomiting, bloody diarrhea, and severe abdominal cramps.
- Third stage is a period of 24 hours during which the victim appears to recover (if hospitalized, the patient is sometimes released!)
- Fourth stage is a relapse, during which kidney and liver failure often occurs, leading to death. Patients may also “bleed out” and die due to the destruction of clotting factors in the blood. There may be more than one relapse.
If you have any reason to suspect that someone has ingested an amanitin-containing mushroom, DON’T WAIT for symptoms to appear! There is no antidote for amanitin poisoning, and the best hope is to rush the person to the hospital where the toxins can be removed before being fully absorbed into the body.
Treatment is largely supportive and symptomatic. Penicillin, kutkin, and silibinin/silymarin show promise as treatments, along with oral activated charcoal and electrolytes. Active measures to treat liver disease are typically followed.
Mushrooms: Gyromitra esculenta and possibly G. ambigua, G. infula. Note Several additional Gyromitra spp., notably G. montanum, G. gigas, G. fastigiata (=brunnea), G. californica, G. sphaerospora and also many related Ascomycetes, such as some species of Helvella, Verpa, and Cudonia spp., even Morels can cause upset if consumed raw or not thoroughly cooked, though the toxins are not clearly known in most cases.
|Gyromitra esculenta||Gyromitra infula||Gyromitra montanum||Helvella lacunosa|
Gyromitrin's product of hydrolisis is monomethylhydrazine (MMH), a colorless, volatile, highly toxic, carcinogenic compound, first discovered and used for it's hypergolic properties in combination with nitrogen tetroxide. MMH is used by NASA as rocket fuel, which should give some idea of what is meant by "volatile".
"Volatile" also means that gyromitrin has a low boiling point, and thus mushrooms containing it can have a puzzling non-effect on some, whereas others are severely poisoned. In Europe, it has sometimes only been the cooks who have died from Gyromitra esculenta. The dividing line between a "safe and "lethal dose" is very slim.
Symptoms appear within 2 to 24 hours and include headaches, abdominal distress, severe diarrhea, and vomiting. In severe cases, liver, kidney, and red blood cell damage may occur, possibly resulting in death. Treatment is largely supportive, and a physician should be consulted.
Gyromitrin is also a known carcinogen, so consuming a less than toxic dose may also cause trouble down the line.
Mushrooms: Cortinarius orellanusand C. rubellus (=C. orellanoides, C. speciosissimus, C. rainierensis). C. splendens, C. atrovirens, C. venenosus, C. gentilis may possibly cause orellanine like poisoning.
Extremely Serious. Onset of symptoms from orellanine poisoning can be very greatly delayed (as much as three weeks), the toxin isn't very well understood, and specific treatments are not available. No cases have been reported from North America as of 2008, but a number of deaths from both C. orellanus and C. rubellus (identified in the literature at the time as C. orellanoides and C. speciosissimus) have occurred in Europe. C. rubellus is found in North America.
Symptoms occur within 36 hours to 3 weeks of ingestion (average is about 8 days), and include nausea, vomiting, lethargy, anorexia, frequent urination, burning thirst, headache, sensations of coldness and shivering (fever generally absent), evidence or progressive kidney failure.
Beyond the standard management of kidney failure, there is little but supportive treatment of use in cases of orellanine poisoning. Patients with severe, but not irreversible damage may begin to recover kidney function between two and four weeks after the onset of symptoms. NOTE: The compounds involved in this syndrome show a very strong turquoise or blue fluorescence under uv light. Both the mushrooms and tissues of the poisoned individual will exhibit this fluorescence.
Psilocybin, Psilocin, and other Indole Derivatives
Mushrooms: About 20 Psilocybe species including P. cyanescens, P. stuntzii, P. cubensis, and P. semilanceata, several Panaeolous species including P. cyanescens and P. subbalteatus, at least three Gymnopilus species most notably Gymnopilus spectabilis plus at least one Mycena, one Pluteus, one Conocybe and one Inocybe.
These indoles are well-known as hallucinogens, and these mushrooms have played important roles in religion and medicine in some parts of the world, notably in South America. Their properties were "rediscovered" by mycologists in Oaxaca in the 1930s, and studied by mycoethnographers Gordon and Valentina Wasson in the 1950s; their chemistry was documented by Albert Hoffmann.
Both psilocybin and psilocin are found naturally in mushrooms, though their ecological purpose is unknown. In the human body, they affect the serotonergic systems in the brain, and show some cross-tolerance with substances such as LSD.
Onset of symptoms usually occurs within an hour of ingestion, and effects typically last up to four to six hours. Effects are primarily psychological and perceptual, including heightened color perception, emotional effects such as religious ecstasy or anxiety, and sometimes hallucinations or delusions. As with any other psychologically-active substance, mindset and situation can greatly influence psilocybin's subjective effects. Care should be taken not to frighten or upset a person under its influence, and if a victim does become anxious, to reassure them that the effects are temporary. Little research has been done on antitoxins, but tryptophan may have a mitigating effect.
Nausea and vomiting are sometimes associated, but generally occur earlier than the psychological effects, and may be associated with other toxins present in some psilocybin-bearing species, rather than with the indoles themselves. A very few severe reactions, including fevers and deaths, have been reported in contexts of psilocybin poisoning of small children; "grazing" accidents by toddlers should be treated in a hospital.
Perhaps the greatest danger posed by psilocybin as a mycotoxin is that the mycologically ignorant may, in hunting for "magic mushrooms," find themselves consuming something different and far more dangerous. Galerina autumnalis and other amanitoxin-bearing "little brown mushrooms" may be mistaken for hallucinogenic species, and there has even been a report of children inhaling the spores of Lycoperdon puffballs in the hopes of "getting high," only to wreak havoc on their lungs.
Delayed Kidney Damage (Renal Failure)
Allenic Norleucine (2-amino-4,5-hexadienoic acid) Mushroom: Amanita smithiana, A. proxima, A. pseudoporphyria. Note: A second compound, chlorocrotylglycine, may also be toxic.
Amanita smithiana has caused numerous poisonings in the Pacific Northwest, where it is possibly being mistaken for the popular Matsutake, or "Pine Mushroom" Tricholoma magnivelare, to which it bears a superficial resemblance. Many physicians have been quick to attribute these poisonings to orellanine, and indeed there are some obvious similarities in the symptoms. However, onset of symptoms is more rapid in cases of A. smithiana poisoning (between 4 and 11 hours, compared to orellanine with a 36 hour to 3 week onset period). A. smithiana causes gastrointestinal distress, anxiety, chills, cramps, disorientation, kidney failure and sometimes malaise, sweating, weakness, warm feeling, oliguria, polyurea, thirst.
Unknown Toxin. Mushroom: Paxillus involutus
Although rarely reported in North America, poisonings by Paxillus involutus do occur, and the mushroom is common enough to warrant inclusion here. It is the third most common cause of gastrointestinal symptoms in Eastern Europe, where is has a long and unfortunate culinary history. However, the main toxic component in P. involutus causes acute immune-mediated hemolytic anemia.
Hemolytic anemia occurs mainly in individuals who have eaten P. involutus for many years without ill effect. Because the syndrome is related to repeat, long-term exposure to the toxin, poisonings may likely go unrecognized, with the more likely diagnosis being idiopathic immune hemolytic anemia.
It is perhaps warranted to suggest that in cases of idiopathic anemia, especially in patients of Eastern European extraction, that the question of P. involutus consumption be raised.
Mushrooms with coprine: Coprinopsis atramentaria (=Coprinus atramentarius), C. insignis, C. quadrifidus, C. variegatus.
Onset of symptoms is a few minutes after alcohol is consumed by a person who has typically eaten Inky Caps (Coprinopsis atramentaria) from 30 minutes to as long as five days earlier. The symptoms are tachycardia (racing heart) and palpitations, tingling arms and legs, warmth and flushing, and sometimes headache, heavy limbs, salivation.
Other Alcohol Induced Syndromes
Mushrooms: Coprinus comatus, Clitocybe clavipes, Boletus luridus, Morels, Pholiota squarrosa, Armillaria mellea, Pleurotus ostreatus, Boletus edulis, etc.
Symptoms GI distress in susceptible individuals. The delay is up to 5 hours. However, this is not the Antabuse Syndrome of the Inky Cap involving racing heart and warmth, etc.
Rhabdomyolysis. Mushrooms: Tricholoma equestre (=T. flavovirens), Russula subnigricans.
Toxicity from Tricholoma equestre has not been reported from the U.S. and some question whether or not it is dangerous, but consumption of massive quantities of this species in Europe have reportedly resulted in delayed kidney damage, delayed neurotoxicity, and breakdown of muscle fibers with release of myoglobin into the blood stream. The European cases of rhabdomyolysis are associated with respiratory and cardiac (myocarditis) complications leading to death. Myocarditis is an inflammation of the heart muscle. The rhabdomyolysis observed with Russula subnigricans in Japan and Taiwan occurs by a different mechanism than that observed with Tricholoma equestre.
Erythromelalgia. Mushrooms: Clitocybe amoenolens and C. acromelalgia. Similar species include Clitocybe (Lepista) inversa, Clitocybe squamosa, Clitocybe gibba, and Hygrophoropsis aurantiaca.
Saviuc and Danel (Saviuc P, Danel V, “New Syndromes in Mushroom Poisoning.” Toxicol Rev 2006; 25(3):199-209) point out that the erythromelalgia syndrome was described as early as the 19th century in Japan and South Korea with Clitocybe acromelalga and since 1996 in France and later in Italy with Clitocybe amoenolens. Erythromelalgia occurs as a result of a maldistribution of blood flow with extremities of the body (typically nose, fingers and toes) calling for more blood and winding up with so much blood flow through various open vessels that hands and feet and nose receive too much and turn bright red, warm to the touch. The situation is very painful and symptoms can last for months. Onset of symptoms is about 1 week after ingestion of the mushrooms and appears to be caused by acromelic acids, compounds that structurally mimic the neurotransmitter glutamate.
Encephalopathy. Mushrooms: Haplopilus rutilans (=Haplopilus nidulans), Pleurocybella porrigens
A delayed neurotoxicity (degenerative brain disorder) has been reported twice in Germany from with Hapalopilus rutilans (= Hapalopilus nidulans) and could turn up in North America since Hapalopilus nidulans is a small fleshy orangish polypore found in eastern North America that turns purple or lilac when a drop of KOH is placed on the surface.
In Japan in 2004 ingestion of large amounts of Pleurocybella porrigens led to an outbreak of convulsive encephalopathy in patients with a history of chronic renal failure resulting in over a dozen deaths.
Rash. Suillus spp. and sometimes other mushrooms
Simply handling mushrooms can on rare occasion cause a rash and itching similar to reaction to poison oak and poison ivy in sensitive individuals. Reported most frequently for Suillus americanus and similar species.