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Mushroom Toxicosis   667




            Mushroom Toxicosis                                                                     Client Education
                                                                                                          Sheet
  VetBooks.ir                                                                                                         Diseases and   Disorders

                                               •  Isoxazole: acute inebriation followed by coma;
            BASIC INFORMATION
                                                                                    mate receptors triggering CNS stimulation;
                                                generally self-limited              mental dullness; ibotenic acid acts on gluta-
           Definition                                                               combined effects result in hyperesthesia,
           Condition resulting from ingestion of any of   HISTORY, CHIEF COMPLAINT  sedation, intermittent agitation
           a variety of toxic mushrooms; toxic syndrome   •  History  of  exposure;  mushrooms  in  the
           produced  depends on  mushroom type  and   vomitus                      DIAGNOSIS
           amount ingested:                    •  GI:  vomiting,  diarrhea  within  4  hours  of
           •  Gastrointestinal  (GI)  irritant  mushrooms:   ingestion            Diagnostic Overview
             large variety of species          •  Hallucinogenic: dysphoria, vocalization in   Diagnosis is reached when nonspecific disorders
           •  Hallucinogenic mushrooms: Psilocybe spp,   30 minutes to 4 hours of ingestion  (e.g., gastroenteritis, hepatotoxicity, neurologic
             Panaeolus spp                     •  Hepatotoxic: acute, severe vomiting ± diar-  disturbance) are combined with evidence of
           •  Hepatotoxic  mushrooms:  Amanita spp,   rhea in 8-24 hours; apparent recovery, then   exposure, such as mushrooms in vomitus. There
             Galerina spp, Lepiota spp          return of GI signs; evidence of acute liver   is no practical clinical confirmatory test.
           •  Nephrotoxic mushrooms: Cortinarius spp  failure in 24-72 hours; acute kidney injury
           •  Muscarinic mushrooms: Inocybe spp, Clitocybe   possible in severe cases  Differential Diagnosis
             spp                               •  Nephrotoxic:  acute  kidney  injury  12   •  GI, muscarinic: parvoviral enteritis, foreign
           •  Gyromitrin  mushrooms:  Gyromitra spp,   hours to 8 days after exposure, polyuria,     body, garbage toxicosis, organophosphate and
             Helvella crispa, Helvella lacunosa  polydipsia                         carbamate pesticide toxicosis
           •  Isoxazole  mushrooms:  Amanita gemmata,   •  Muscarinic: salivation, vomiting, diarrhea,   •  Hepatotoxic: other toxicoses (acetaminophen,
             Amanita muscaria, Amanita smithiana, Amanita   lacrimation, bradycardia within 4 hours of   iron, blue-green algae, Cycas spp), infectious
             strobiliformis, and Tricholoma muscarium  ingestion                    hepatitis
                                               •  Gyromitrin: GI signs in 6-8 hours, hepatore-  •  Nephrotoxic: ethylene glycol, grapes/raisins,
           Epidemiology                         nal and hemolytic syndrome 36-48 hours   nonsteroidal antiinflammatory drug (NSAID)
           SPECIES, AGE, SEX                    after ingestion                     toxicity, leptospirosis
           All mammalian species are susceptible; dogs   •  Isoxazole: vomiting, ataxia, disorientation,   •  Isoxazole,  hallucinogenic:  encephalitis,
           more likely to ingest than cats      sleep/coma within 4 hours of ingestion  portosystemic shunt, serotonergic drugs,
                                                                                    cannabis, other illicit substances
           GEOGRAPHY AND SEASONALITY           PHYSICAL EXAM FINDINGS
           •  Highest incidence of mushroom poisoning   •  GI: vomiting, diarrhea, dehydration possible,   Initial Database
             (all types) occurs from August to October.  but generally unremarkable  •  CBC, serum biochemistry profile, urinalysis,
           •  GI irritant mushrooms: wide distribution;   •  Hallucinogenic: vocalization, agitation  venous or arterial blood gas measurement:
             long range of fruiting seasons    •  Hepatotoxic: signs of abdominal pain, icterus,   depends on type. Marked increase in liver
           •  Hallucinogenic mushrooms: wide distribu-  hypotension, hepatomegaly, coma  enzymes ± bilirubin; azotemia; hypoglycemia;
             tion;  Pacific  Northwest  and  Gulf  Coast;   •  Nephrotoxic: uremic signs (p. 23)  acidosis
             lawns, gardens, roadsides, open woods;   •  Muscarinic:  vomiting,  hypersalivation,   •  Coagulation  profile:  coagulopathy  with
             cultivated in homes for recreational use  lacrimation, diarrhea, bradycardia, wet lung   severe liver injury; disseminated intravascular
           •  Hepatotoxic mushrooms: wide distribution   sounds                     coagulation (hepatotoxic mushrooms)
             throughout United States; wide variation in   •  Gyromitrin:  vomiting,  abdominal  pain,   •  Rule out differential diagnosis depending on
             habitats and fruiting seasons      icterus, hepatomegaly, hemoglobinuria,   presentation (e.g., leptospirosis serology)
           •  Nephrotoxic mushrooms: common in North   anemia
             America, especially Canada; grows in woods   •  Isoxazole: agitation, tremors, disorientation,   Advanced or Confirmatory Testing
             and forests; uncommon in urban areas  GI signs                       •  Abdominal imaging: hepatomegaly (hepa-
           •  Muscarinic mushrooms: wide distribution;                              totoxic mushrooms)
             forests or fields; fruits in fall, early winter in   Etiology and Pathophysiology  •  Liver biopsy (hepatotoxic): liver necrosis
             temperate areas, year-round in warm, moist   •  GI:  several  mechanisms;  hypersensitivity,   •  Urine: amatoxins can be detected in the urine
             climates                           local irritation                    as early as 90-120 minutes after ingestion
           •  Gyromitrin mushrooms: throughout North   •  Hallucinogenic:  stimulate  serotonin  and   of an amatoxin-containing mushroom.
             America, primarily in the spring   possibly norepinephrine receptors in central   •  Urine: muscimol can be detected in urine;
           •  Isoxazole mushrooms: eastern United States   and peripheral nervous systems  turnaround time is long and little value in
             and  Pacific  Northwest;  forests;  fruits  in   •  Hepatotoxic:  cyclopeptides  interfere  with   acute cases
             spring/early summer and again in fall  DNA synthesis, protein synthesis, resulting
                                                in cellular necrosis               TREATMENT
           Clinical Presentation               •  Nephrotoxic:  orellanine  causes  energy
           DISEASE FORMS/SUBTYPES               depletion and tubulointerstitial nephritis;   Treatment Overview
           •  GI: acute, self-limited GI distress  cortinarin causes oxidative membrane injury  Initially, manage potentially life-threatening
           •  Hallucinogenic: acute central nervous system   •  Muscarinic: bind muscarinic acetylcholine   abnormalities (e.g., seizures, hypoglycemia,
             (CNS) signs; generally self-limited  receptors in parasympathetic nervous system;   bleeding  disorders).  Further  treatment  con-
           •  Hepatotoxic: acute GI signs, then liver failure   prolonged duration due to lack of degrada-  sists of decontamination and supportive care:
             in 24-72 hours                     tion; does not inhibit acetylcholinesterase  induction of vomiting and administration of
           •  Nephrotoxic: renal tubular dysfunction  •  Gyromitrin:  metabolized  to  monomethyl-  activated charcoal to minimize absorption and
           •  Muscarinic: acute muscarinic signs  hydrazine, leading to metabolic alterations  treatment to minimize hepatic/renal injury,
           •  Gyromitrin: GI signs followed by neurologic,   •  Isoxazole:  muscimol  mimics  gamma-  excessive muscarinic effects, and complications
             hepatorenal, and/or hemolytic syndromes  aminobutyric acid (GABA), causing sedation,   as they arise.

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