Mushroom poisoning: A proposed new clinical classification.

Diagnostic algorithm Hepatotoxicity Mushroom poisoning Mushrooms Poisonous mushrooms Renal failure Rhabdomyolysis

Journal

Toxicon : official journal of the International Society on Toxinology
ISSN: 1879-3150
Titre abrégé: Toxicon
Pays: England
ID NLM: 1307333

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 23 03 2018
revised: 30 10 2018
accepted: 07 11 2018
pubmed: 16 11 2018
medline: 12 1 2019
entrez: 16 11 2018
Statut: ppublish

Résumé

Mushroom poisoning is a significant and increasing form of toxin-induced-disease. Existing classifications of mushroom poisoning do not include more recently described new syndromes of mushroom poisoning and this can impede the diagnostic process. We reviewed the literature on mushroom poisoning, concentrating on the period since the current major classification published in 1994, to identify all new syndromes of poisoning and organise them into a new integrated classification, supported by a new diagnostic algorithm. New syndromes were eligible for inclusion if there was sufficient detail about both causation and clinical descriptions. Criteria included: identity of mushrooms, clinical profile, epidemiology, and the distinctive features of poisoning in comparison with previously documented syndromes. We propose 6 major groups based on key clinical features relevant in distinguishing between poisoning syndromes. Some clinical features, notably gastrointestinal symptoms, are common to many mushroom poisoning syndromes. Group 1 - Cytotoxic mushroom poisoning. Syndromes with specific major internal organ pathology: (Subgroup 1.1; Primary hepatotoxicity); 1A, primary hepatotoxicity (amatoxins); (Subgroup 1.2; Primary nephrotoxicity); 1B, early primary nephrotoxicity (amino hexadienoic acid; AHDA); 1C, delayed primary nephrotoxicity (orellanines). Group 2 - Neurotoxic mushroom poisoning. Syndromes with primary neurotoxicity: 2A, hallucinogenic mushrooms (psilocybins and related toxins); 2B, autonomic-toxicity mushrooms (muscarines); 2C, CNS-toxicity mushrooms (ibotenic acid/muscimol); 2D, morel neurologic syndrome (Morchella spp.). Group 3 - Myotoxic mushroom poisoning. Syndromes with rhabdomyolysis as the primary feature: 3A, rapid onset (Russula spp.); 3B, delayed onset (Tricholoma spp.). Group 4 - Metabolic, endocrine and related toxicity mushroom poisoning. Syndromes with a variety of clinical presentations affecting metabolic and/or endocrine processes: 4A, GABA-blocking mushroom poisoning (gyromitrins); 4B, disulfiram-like (coprines); 4C, polyporic mushroom poisoning (polyporic acid); 4D, trichothecene mushroom poisoning (Podostroma spp.); 4E, hypoglycaemic mushroom poisoning (Trogia venenata); 4F, hyperprocalcitoninemia mushroom poisoning (Boletus satanas); 4G, pancytopenic mushroom poisoning (Ganoderma neojaponicum). Group 5 - Gastrointestinal irritant mushroom poisoning. This group includes a wide variety of mushrooms that cause gastrointestinal effects without causing other clinically significant effects. Group 6 - Miscellaneous adverse reactions to mushrooms. Syndromes which do not fit within the previous 5 groups: 6A, Shiitake mushroom dermatitis; 6B, erythromelagic mushrooms (Clitocybe acromelagia); 6C, Paxillus syndrome (Paxillus involutus); 6D, encephalopathy syndrome (Pleurocybella porrigens).

Identifiants

pubmed: 30439442
pii: S0041-0101(18)30728-1
doi: 10.1016/j.toxicon.2018.11.007
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-65

Commentaires et corrections

Type : CommentIn

Informations de copyright

Crown Copyright © 2018. Published by Elsevier Ltd. All rights reserved.

Auteurs

Julian White (J)

Toxinology Dept., Women's & Children's Hospital, North Adelaide, Australia. Electronic address: julian.white@adelaide.edu.au.

Scott A Weinstein (SA)

Toxinology Dept., Women's & Children's Hospital, North Adelaide, Australia.

Luc De Haro (L)

Marseille Poison Centre, Hopital Sainte Marguerite, Marseille, France.

Regis Bédry (R)

Hospital Secure Unit, Pellegrin University Hospital, Bordeaux, France.

Andreas Schaper (A)

GIZ-Nord Poisons Centre, University Medical Center Göettingen, Göttingen, Germany.

Barry H Rumack (BH)

Department of Emergency Medicine and Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.

Thomas Zilker (T)

Dept. for Clinical Toxicology at II, Med. Klinik, TU, München, Munich, Germany.

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