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<article article-type="case-report" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Our Dermatol Online</journal-id>
<journal-title>Our Dermatol Online</journal-title>
<issn pub-type="epub">2081-9390</issn>
<publisher>
<publisher-name>Our Dermatology Online</publisher-name>
<publisher-loc>Poland</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">OURD-8-179</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20172.48</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Recurrent erythema multiforme with arthritis &#x2013; A rare association</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Bhat</surname>
<given-names>Yasmeen Jabeen</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zeerak</surname>
<given-names>Sumaya</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Baba</surname>
<given-names>Asif Nazir</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hassan</surname>
<given-names>Iffat</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wani</surname>
<given-names>Roohi</given-names>
</name>
<xref ref-type="aff" rid="aff3">3</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label><italic>Departments of Dermatology, STD &#x0026; Leprosy, Government Medical College, University of Kashmir, Srinagar, India</italic></aff>
<aff id="aff2"><label>2</label><italic>Departments of Orthopedics, Government Medical College, University of Kashmir, Srinagar, India</italic></aff>
<aff id="aff3"><label>3</label><italic>Departments of Pathology, Government Medical College, University of Kashmir, Srinagar, India</italic></aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding author:</bold> Dr. Yasmeen Jabeen Bhat, E-mail: <email xlink:href="yasmeenasif76@gmail.com">yasmeenasif76@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2017</year>
</pub-date>
<volume>8</volume>
<issue>2</issue>
<fpage>179</fpage>
<lpage>182</lpage>
<history>
<date date-type="received"><day>05</day><month>07</month><year>2016</year></date>
<date date-type="accepted"><day>29</day><month>08</month><year>2016</year></date>
</history>
<permissions>
<copyright-statement>Copyright: &#x000a9; Our Dermatol Online 2</copyright-statement>
<copyright-year>2017</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
</license>
</permissions>
<abstract>
<p>Erythema multiforme (EM) is an acute, immune-mediated, self-limiting mucocutaneous condition characterized by distinctive target lesions. The etiology is diverse and numerous diseases have been associated with EM. However, arthritis has been rarely reported with it. We report a rare association between EM, localized mainly over the joints, and polyarthritis in a male patient, who responded successfully to oral acyclovir.</p>
</abstract>
<kwd-group>
<kwd>Erythema multiforme</kwd>
<kwd>Recurrent</kwd>
<kwd>Arthritis</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec>
<title/>
<p><bold>What&#x2019;s Known:</bold> Erythema multiforme minor is rarely associated with arthritis.</p>
</sec>
<sec id="sec1-1" sec-type="intro">
<title>INTRODUCTION</title>
<p>Erythema multiforme (EM) is an acute, immune-mediated, self-limited mucocutaneous condition characterized by distinctive target lesions with concentric colour variations [<xref ref-type="bibr" rid="ref1">1</xref>-<xref ref-type="bibr" rid="ref3">3</xref>]. It is believed to be the result of a type four hypersensitivity reaction, occuring as a consequence to an underlying trigger. It can occur as a single episode or the lesions can recur in the form of multiple episodes, with a highly variable interval between these episodes [<xref ref-type="bibr" rid="ref2">2</xref>]. In those patients where EM has a remitting &#x2013;relapsing course, over months or years, the condition is known as recurrent erythema multiforme [<xref ref-type="bibr" rid="ref1">1</xref>]. This causes significant distress to the patient, necessitating a thorough search for the underlying trigger. Erythema multiforme can have association with a variety of diseases [<xref ref-type="bibr" rid="ref4">4</xref>]. Here we report a rare association between EM and polyarthritis in a male patient.</p>
</sec>
<sec id="sec1-2" sec-type="cases">
<title>CASE REPORT</title>
<p>A 25 years old male patient, reported to our dermatology OPD with the complaints of red, raised lesions over the joints of both hands, feet, elbows, knees and ankles with pain and swelling of the small joints of hand. These lesions had been appearing for the last 3 years, with a remitting and relapsing course. As per the patient, the lesions had first appeared over the joints of his hands nearly 3 years ago and were associated with pain and swelling of these joints. The eruption was preceeded by fever and the patient had associated constitutional symptoms also. The episode lasted for a few days at that time. This was followed by a period of remission, lasting for a few weeks. Soon the patient developed fresh lesions over his hand joints again, followed by the joints of feet, elbows and knees. These lesions had the same course as above but the extent was widespread with severe pain, swelling and limited movements of the affected joints of hands, feet, elbows and knees. Multiple such episodes following the same course, occurred over the subsequent three years, with periods of remission in between. An interesting finding was the exacerbation of lesions during cold weather with a history of recurrent oral herpes often preceeding the cutaneous eruption. There was no significant drug intake prior to the appearance of lesions. Moreover the joint involvement had started with the cutaneous eruption and was not present before 3 years. There was no history of morning stiffness or any other significant complaint in the history.</p>
<p>On examination, the general physical examination was found to be unremarkable. The cutaneous examination revealed multiple erythematous to violaceous crusted papules, erosions, pustules and atypical target lesions distributed over the arms, forearms (extensor surfaces), hands (including dorsa of both hands, dorsal and palmar surfaces of fingers especially over metacarpophalangeal, proximal and distal interphalangeal joints), knees, lower legs, dorsa of both feet (predominantly over the metatarsophalangeal and interphalangeal joints of feet) (Figs <xref ref-type="fig" rid="F1">1</xref> - <xref ref-type="fig" rid="F3">3</xref>). The interphalangeal joints of left thumb and index finger along with the joints of knee, elbow, feet were erythematous and swollen, tender, with reduced range of movements. The surface temperature was also raised. No mucosal lesion was present.</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Atypical target lesions on the hands involving mainly the joints.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-179-g001.tif"/>
</fig>
<fig id="F2">
<label>Figure 2</label>
<caption>
<p>Inflammed left proximal interphalingeal joint of index finger and thumb.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-179-g002.tif"/>
</fig>
<fig id="F3">
<label>Figure 3</label>
<caption>
<p>Target lesions on palmar aspect of hands.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-179-g003.tif"/>
</fig>
<p>The routine haematological investigations were within normal limits including ASO titre and C- reactive protein. Serum anti- nuclear antibody, rheumatoid factor and anti- CCP (anti- citrullinated peptide) levels were also done, which were all negative. Serum IgG and IgM anti-HSV 1 were positive. X-rays of the affected joints revealed mild soft tissue edema. A histopathological examination of the cutaneous lesions was performed and the features were consistent with the diagnosis of erythema multiforme (<xref ref-type="fig" rid="F4">Fig. 4</xref>).</p>
<fig id="F4">
<label>Figure 4</label>
<caption>
<p>Involvement of knee joints.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-179-g004.tif"/>
</fig>
<p>Following this, the patient was put on oral acyclovir 400mg tid. The cutaneous lesions as well as the arthritis resolved within a period of two weeks (<xref ref-type="fig" rid="F5">Fig. 5</xref>). The patient was put on suppressive therapy for herpes simplex for six months and was free of lesions for this period and next six months.</p>
<fig id="F5">
<label>Figure 5</label>
<caption>
<p>Resolution of lesions and joint swelling after two weeks of acyclovir intake.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-179-g005.tif"/>
</fig>
</sec>
<sec id="sec1-3" sec-type="discussion">
<title>DISCUSSION</title>
<p>First described by Ferdinand von Hebra in 1866, erythema multiforme is an acute, mucocutaneous disorder considered to be a hypersensitivity reaction associated with certain infections and medications [<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref5">5</xref>]. It is characterized by acrally distributed, distinct targetoid lesions with concentric color variation, sometimes accompanied by oral, genital, or ocular mucosal erosions or a combination of these [<xref ref-type="bibr" rid="ref6">6</xref>]. The etiology is diverse with a huge list of causative agents reported in literature. The main causes include infections, medication use, malignancy, autoimmune disease, radiation, immunization, and menstruation [<xref ref-type="bibr" rid="ref2">2</xref>]. In addition, numerous other agents have been incriminated and numerous disease associations reported.</p>
<p>Viral infection, especially by herpes simplex virus is believed to be one of the most common etiological agents for EM with studies reporting a 70&#x0025; causality of EM due to this virus alone [<xref ref-type="bibr" rid="ref7">7</xref>,<xref ref-type="bibr" rid="ref8">8</xref>]. A distinct term has been coined for such cases where the virus is responsible for recurrent episodes of EM, namely herpes- associated EM (HAEM) [<xref ref-type="bibr" rid="ref9">9</xref>].</p>
<p>Even though numerous diseases, both immunological and non- immunological have been associated with EM, arthritis has been rarely associated with it. Contrary to the arthralgias seen in most of the EM patients, our patient had features of arthritis with no evidence of any connective tissue disorder. Although herpes group of viruses is most commonly attributed etiological agent of connective tissue disorders like SLE and RA, but studies show no statistical significance of HSV 1 and 2 serology in these patients and the healthy controls [<xref ref-type="bibr" rid="ref10">10</xref>,<xref ref-type="bibr" rid="ref11">11</xref>].</p>
<p>In our patient, the remitting and relapsing course of the disease, history of orolabial herpes often preceding the eruption and constitutional symptoms, all favoured the viral etiology of erythema multiforme. However the preponderance of lesions over the joints of upper and lower limbs with associated features of arthritis in the hand joints was a unique association.</p>
<p>Recurrent EM has been treated successfully with a number of drugs, including oral antiviral drugs [<xref ref-type="bibr" rid="ref12">12</xref>]. A similar case was reported wherein the recurrent cutaneous lesions of erythema multiforme and polyarthritis responded to oral acyclovir [<xref ref-type="bibr" rid="ref13">13</xref>]. The resolution of the cutaneous lesions as well as the arthritis with anti-viral drugs could be due to the common pathogenesis of the two conditions which would require further studies.</p>
<p><bold>What&#x2019;s new:</bold> Recurrent erythema multiforme minor was associated with polyarthritis repeatedly in the same joints, that too responded to oral antiviral therapy.</p>
<sec id="sec2-1">
<title>Consent</title>
<p>The examination of the patient was conducted according to the Declaration of Helsinki principles.</p>
</sec>
</sec>
</body>
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<fn-group>
<fn fn-type="supported-by">
<p><bold>Source of Support:</bold> Nil</p>
</fn>
<fn fn-type="conflict">
<p><bold>Conflict of Interest:</bold> None declared.</p>
</fn>
</fn-group>
</back>
</article>
