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Vol 16, No 2
Table of Contents

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<p class="frontmatter-fieldnotes disclaimernew" style="margin-bottom:15px;">This work may not be copied, distributed, displayed, published, reproduced, transmitted, modified, posted, sold, licensed, or used for commercial purposes. By downloading this file, you are agreeing to the publisher’s <a href="/pages/termsofuse.aspx" target="_blank">Terms & Conditions</a>.</p> <div id="x13l01580">
  <div class="story">
    <p class="ltrs-br-ltr-br-title"><span class="bold">Lithium-Induced Fixed Drug Eruption in a Case of Bipolar Mania</span></p>
    <p class="ltrs-br-ltr-br-body-text"><span class="semibold">To the Editor:</span> Lithium is one of the commonly used drugs for the treatment of bipolar affective disorders. Its use is associated with various side effects, dermatologic side effects being one of them. Dermatologic side effects can be one of the reasons for poor compliance and are reported in 3%–45% of the population receiving lithium. Mohandas and Rajmohan<span class="htm-cite"><a href="#ref1">1</a></span> found acneiform eruptions, psoriasis, maculopapular eruptions, and follicular eruptions to be most commonly reported. However, fixed drug eruption due to the use of lithium carbonate has not been reported. We report one such case in a patient with bipolar mania.</p>
    <p class="ltrs-br-ltr-br-body-text">&nbsp;</p>
    <p class="ltrs-br-ltr-br-body-text"><span class="semibold-ital">Case report.</span> Mr A, a 16-year-old male diagnosed with bipolar affective disorder as the second episode of mania with psychotic symptoms according to <span class="italic">ICD-10 </span>criteria, reported for follow-up. A maintenance dose of tablet lithium carbonate 900 mg/d was effective until the past year. At this visit, he reported blisters over the dorsal aspects of the hands and foot, with lesions extending to the mouth and genitalia. After 2–3 days, the blisters had subsided and were now seen to have been replaced by a hypopigmented patch surrounded by hyperpigmented border over the same areas (<span class="callout"><a href="#" onclick="createFigure('f1'); return false;">Figure 1</a></span>). The lesions were associated with itching and disappeared after a few days of treatment with povidone-iodine (Betadine) application and multivitamin capsules. </p>
    <div id="figure" class="right"> <a href="#" onclick="createFigure('f1'); return false;"><img src="13l01580F1.jpg" alt="Figure 1" id="f1" border="0" /></a>
      <p class="click-to-enlarge">Click figure to enlarge</p>
    </div>
    <p class="ltrs-br-ltr-br-body-text">Mr A attributed the lesions to the antidiarrheal medication taken during one of those instances and continued taking lithium carbonate in the same dose. His serum lithium level was within the therapeutic range at this visit. However, the lesions recurred in a similar manner a month later on 2 successive occasions. On consultation, lithium carbonate therapy was stopped because lithium carbonate was considered the possible precipitant. A rechallenge was done in a low dose, after which the lesions appeared again, thereby confirming lithium to be the likely cause. The Naranjo Adverse Drug Reaction Probability Scale<span class="htm-cite"><a href="#ref2">2</a></span> was applied with a score of 6, suggesting that lithium carbonate was the probable cause of the side effect. Mr A was subsequently started on tablet sodium valproate (1,000 mg/d) and olanzapine (10 mg/d). He was maintaining well for 4 months after the change in medications but was lost to follow-up. </p>
    <p class="ltrs-br-ltr-br-body-text">&nbsp;</p>
    <p class="ltrs-br-ltr-br-body-text">The exact cause for the cutaneous side effects associated with lithium is not known, but the role of stress and psychological factors has been proposed. Kansal et al<span class="htm-cite"><a href="#ref3">3</a></span> state that the decrease in cyclic adenosine monophosphate and inositol that results from lithium treatment has also been considered as a possible cause. The low intracellular levels of calcium, the lack of differentiation of keratinocytes, and enhanced phagocytic activity of leukocytes have been suggested as the possible mechanisms of action. Reduction in the dosage apart from specific intervention for the lesions has been suggested as a possible treatment strategy.</p>
    <p class="ltrs-br-ltr-br-references-head"><span class="smallcaps">References</span></p>
    <p class="references-references-text-1-9"><a name="ref1"></a>1. Mohandas E, Rajmohan V. Lithium use in special populations. <span class="italic">Indian J Psychiatry</span>. 2007;49(3):211–218. <span class="pubmed-crossref"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=20661390&dopt=Abstract">PubMed</a> <a href="http://dx.doi.org/10.4103/0019-5545.37325">doi:10.4103/0019-5545.37325</a></span></p>
    <p class="references-references-text-1-9"><a name="ref2"></a>2. Naranjo CA, Busto U, Sellers EM, et al. A method for estimating the probability of adverse drug reactions. <span class="italic">Clin Pharmacol Ther</span>. 1981;30(2):239–245.<span class="pubmed-crossref"> <a href="http://www.ncbi.nlm.nih.gov/pubmed/?term=Naranjo+CA%2C+Busto+U%2C+Sellers+EM%2C+et+al.+A+method+for+estimating+the+probability+of+adverse+drug+reactions.+Clin+Pharmacol+Ther.+1981%3B30%3A239%E2%80%93245">PubMed</a></span></p>
    <p class="references-references-text-1-9"><a name="ref3"></a>3. Kansal NK, Chawla O, Singh A, et al. The cutaneous adverse effects of lithium. <span class="italic">J&nbsp;Clin Diagn Res</span>. 2011;5(3):570–572.</p>
    <p class="ltrs-br-ltr-br-author" style="margin-top:15px;" ><span class="bold">Varun Shantilal Mehta, MD</span></p>
    <p class="ltrs-br-ltr-br-author"><a href="mailto:vs_mehta@yahoo.co.in" target="_blank">vs_mehta@yahoo.co.in</a></p>
    <p class="ltrs-br-ltr-br-author"><span class="bold">Sanjay Raj, DPM</span></p>
    <p class="ltrs-br-ltr-br-author"><span class="bold">Sachchidanand Singh, MD</span></p>
    <p class="ltrs-br-ltr-br-author"><span class="bold">Vinod Sinha, DPM, MD</span></p>
    <p class="ltrs-br-ltr-br-endmatter-fieldnotes"><span class="semibold-ital">Author affiliations:</span> Department of Psychiatry, Central Institute of Psychiatry, Ranchi, India.</p>
    <p class="ltrs-br-ltr-br-endmatter-fieldnotes"><span class="semibold-ital">Potential conflicts of interest: </span>None reported.</p>
    <p class="ltrs-br-ltr-br-endmatter-fieldnotes"><span class="semibold-ital">Funding/support: </span>None reported.</p>
    <p class="ltrs-br-ltr-br-endmatter-fieldnotes"><span class="semibold-ital">Published online:</span> April 17, 2014.</p>
    <p class="ltrs-br-ltr-br-copyright-doi"><span class="italic">Prim Care Companion CNS Disord 2014;16(2):</span><span class="doi">doi:10.4088/PCC.13l01580</span></p>
    <p class="ltrs-br-ltr-br-copyright-doi"><span class="italic">© Copyright 2014 Physicians Postgraduate Press, Inc.</span></p>
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