<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2015.410068</article-id><article-id pub-id-type="publisher-id">CRCM-60754</article-id><article-categories><subj-group subj-group-type="heading"><subject>Short Report</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Severe Colchicine Poisoning: A Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>bdelkarim</surname><given-names>Shimi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Soumaya</surname><given-names>Touzani</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ali</surname><given-names>Derkaoui</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohammed</surname><given-names>Khatouf</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Intensive Care Unit A1, Hassan II University Hospital, Sidi Mohamed Ben Abdellah University, Fez, Morocco</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>akshimi@gmail.com(BS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>12</day><month>10</month><year>2015</year></pub-date><volume>04</volume><issue>10</issue><fpage>342</fpage><lpage>344</lpage><history><date date-type="received"><day>7</day>	<month>September</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>26</month>	<year>October</year>	</date><date date-type="accepted"><day>29</day>	<month>October</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Colchicine intoxication is uncommon but potentially life threatening because of the high toxicity of the drug. Colchicine binds to the intracellular protein tubulin, causing disturbed mitosis in all tissues followed by multi-organ failure. Case Presentation: We report a case of a 23-year-old woman admitted to emergency room 12 hours after a suicide attempt by ingestion of approximatively 40 mg of colchicine. Few hours after consumption, first symptoms were a hemodynamic shock and ARDS, leading to her death due to multi-organ failure. Conclusion: The colchicine intoxication has strong morbidity for doses higher than 0.5 mg/kg. The treatment is symptomatic. The immunotherapy using anti-colchicine allows improving critical form’s prognosis.
 
</p></abstract><kwd-group><kwd>Colchicine</kwd><kwd> Intoxication</kwd><kwd> Shock</kwd><kwd> Multiple Organ Failure</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>First isolated from Colchicum autumnale by Joseph Pelletier and Joseph Bienaim&#233; Caventou in 1820, but falsely identified as veratrine, colchicine was only isolated as a pure and crystalline form by Alfred Houd&#233; in 1884 [<xref ref-type="bibr" rid="scirp.60754-ref1">1</xref>] . It’s registered for the treatment of acute gout. It’s also used to treat familial Mediterranean fever, Beh&#231;et disease, sarcoidosis, psoriasis, sclerodermia and amyloidosis [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.60754-ref3">3</xref>] . Acute colchicines-intoxication (CI) is rare and it leads to multi-visceral failure. It has a narrow therapeutic index, with no clear-cut distinction among nontoxic, toxic and lethal doses [<xref ref-type="bibr" rid="scirp.60754-ref1">1</xref>] . CI severity depends on ingested doses. However, low-doses (5 - 10 mg) are fatal [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] . We discuss a 23-year-old patient who ingested colchicine for suicidal purpose.</p></sec><sec id="s2"><title>2. Case Description</title><p>A 23-year-old woman with an unremarkable medical history came to the emergency room, 18 hours after a suicide attempt by ingestion of an estimated 40 mg of colchicine (0.68 mg per kilogram bodyweight). The symptoms were: diffuse abdominal pain, diarrhea and vomiting. On admission, her Glasgow coma scale was 15. Her blood pressure was 95/57, pulse rate 125/minute. She was eupneic with oxygen saturation 98% while breating 4 litres of O<sub>2</sub>.</p><p>Gastric wash was achieved. Four-hours later, the patient presented shock state, frissons and profuse sweating. The blood pressure was 65/38 mmHg. The patient was admitted to the intensive care unit because hemodynamic instability with signs of multi-organ failure. Supportive treatment, including volume resuscitation and administration of norepinephrine and dobutamine, was started.</p><p>Laboratory results revealed a hemoglobin at 10.5 g/dl, leucocytosis of 56,000 elements/mm, platelets-rate of 23,700 elements/mm. The renal function was slightly disturbed with urea rate at 0.89 g/l, the creatinine was 25 mg/l and the transaminase was multiplied by 2. The prothrombin rate was 28% and the troponine 3.8. Arterial blood gas analysis showed a pH of 7.19 and a lactate level at 11.7 mmol/l.</p><p>After 24 hours, the patient developed respiratory insufficiency due to acute respiratory distress syndrome (ARDS) and was intubated. The electrocardiogramme showed diffuse repolarization disorders. The evolution was fatal with multi-organ failure despite the considered reanimation measures.</p></sec><sec id="s3"><title>3. Discussion</title><p>The colchicine is an alkaloid extracted from colchicum and Gloriosa-superb plants belonging to spindle poisons family. Colchicine has a narrow therapeutic index, with no clear-cut distinction between nontoxic, toxic and lethal doses [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] . Ingestion of more than 0.5 mg/kg of colchicine per kilogram body weight causes serious side effects and can even be fatal [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] . Lethal intoxication cases have been reported after ingestion of only 7 mg of colchicine [<xref ref-type="bibr" rid="scirp.60754-ref4">4</xref>] .</p><p>Colchicine is a neutral lipophylic alkaloid with mild anti inflammatory activity and strong anti mitotic activity [<xref ref-type="bibr" rid="scirp.60754-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] . Cochicine is rapidly absorbed from the gastro intestinal tract and is rapidly distributed to all tissues [<xref ref-type="bibr" rid="scirp.60754-ref2">2</xref>] . The colchicine’s toxicity is due to its prolonged but reversible fixation on tubulin wich, under this form, cannot be polymerized into microtubules. This property is responsible for cytostatic effect with cellular functions inhibition which is connected to inflammation mechanisms [<xref ref-type="bibr" rid="scirp.60754-ref1">1</xref>] .</p><p>The toxic effects of colchicine occur in three stages: 1―Gastro intestinal phase occurring within the first few hours of ingestion which may result in volume depletion and hypotension; 2―Multiple organ failure developing after 1 - 3 days; and 3―the recovery phase in which most affected organs start to show sign of improvement by the 10<sup>th</sup> day [<xref ref-type="bibr" rid="scirp.60754-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.60754-ref6">6</xref>] .</p><p>The colchicine intoxication has strong morbidity for doses higher than 0.5 mg/kg. The main symptoms are digestive disorders and decreased coagulation factors. Doses between 0.5 and 0.8 mg/kg are related to a death risk of 10% with additional medullar aplasia. Doses higher to 0.8 mg/kg are fatal with major refractory circulatory deficiency in 72 hours [<xref ref-type="bibr" rid="scirp.60754-ref7">7</xref>] . Our patient ingested 40 mg, which caused hemodynamic failure at first and then a multivisceral failure after 24 hours of admission.</p><p>Treatment is basically supportive. However, a recent effective experimental therapy including F (a,b) fragments of anti-colchicine antibodies was reported [<xref ref-type="bibr" rid="scirp.60754-ref8">8</xref>] . Colchicine specific Fab fragments consist of the light chain and variable region of the heavy chain and are derived from goats [<xref ref-type="bibr" rid="scirp.60754-ref9">9</xref>] . Their mechanism of action is similar to that of digoxin specific Fab fragments. There is a high affinity between the Fab fragment and colchicine and this acts to prevent the drug returning to these peripheral binding sites [<xref ref-type="bibr" rid="scirp.60754-ref10">10</xref>] .</p></sec><sec id="s4"><title>4. Conclusion</title><p>Colchicine intoxication is a life threatening condition. Colchicine binds to the intracellular protein tubulin causing disturbed mitosis in all tissues followed by multi-organ failure. The colchicine intoxication is responsible of high mortality with acute complications. The immunotherapy using F(a,b) anticolchicine allows improving critical form’s prognosis.</p></sec><sec id="s5"><title>Statement</title><p>No potential conflict of interest relevant to this article were reported or known.</p></sec><sec id="s6"><title>Cite this paper</title><p>AbdelkarimShimi,SoumayaTouzani,AliDerkaoui,MohammedKhatouf, (2015) Severe Colchicine Poisoning: A Case Report. 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