<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.3 20070202//EN" "journalpublishing.dtd">
<article article-type="letter" 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-8-100</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20171.27</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Letter to the Editor</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Chromoblastomycosis: Report of a case from a non-endemic region</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Hadj</surname>
<given-names>Olfa El Amine El</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Msakni</surname>
<given-names>Issam</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lamine</surname>
<given-names>Fehmi</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Laabidi</surname>
<given-names>Besma</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bouzai&#x00E8;ne</surname>
<given-names>Ammar</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label><italic>Immuno-Histo-Pathological Department Salah Azaiez Institute, Tunis, Tunisia</italic></aff>
<aff id="aff2"><label>2</label><italic>Pathological Department, Military Hospital, Tunis, Tunisia</italic></aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding author:</bold> Dr. Olfa El Amine El Hadj, E-mail: <email xlink:href="olfaelamine@yahoo.fr">olfaelamine@yahoo.fr</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2017</year>
</pub-date>
<volume>8</volume>
<issue>1</issue>
<fpage>100</fpage>
<lpage>101</lpage>
<history>
<date date-type="received"><day>05</day><month>06</month><year>2016</year></date>
<date date-type="accepted"><day>20</day><month>08</month><year>2016</year></date>
</history>
<permissions>
<copyright-statement>Copyright: &#x000a9; Our Dermatol Online 1</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>
</article-meta>
</front>
<body>
<sec id="sec1-1">
<title/>
<p>Sir,</p>
<p>Chromoblastomycosis is a chronic fungal infection prevalent in tropical regions, but rare in Tunisia. It causes some diagnostic difficulties. We report the third case of a Tunisian man.</p>
<p>A 47-year-old man presented with a skin lesion, of 3 years duration, located in the right limb. The lesion gradually expanded to form a 20 cm violet-colored papule with an atrophic center (<xref ref-type="fig" rid="F1">Fig. 1</xref>). The diagnosis of cutaneous tuberculosis was suspected. Cultures were negative. A deep skin biopsy revealed the presence of fungal elements within a granulomatous reaction (Figs. <xref ref-type="fig" rid="F2">2</xref> and <xref ref-type="fig" rid="F3">3</xref>). There was no evidence of any immunodeficiency.</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Violet-colored papule with an atrophic center.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-100-g001.tif"/>
</fig>
<fig id="F2">
<label>Figure 2</label>
<caption>
<p>Biopsy showed hyperpasic epidermis within a granulomatous reaction in the dermis.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-100-g002.tif"/>
</fig>
<fig id="F3">
<label>Figure 3</label>
<caption>
<p>A deep skin biopsy revealed the presence of fungal elements.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-100-g003.tif"/>
</fig>
<p>In the Maghreb countries, chromomycosis is rare. Among 30 observations of deep mycoses in Morocco, only 5 patients presented chromomycosis [<xref ref-type="bibr" rid="ref1">1</xref>]. Eight cases have been reported in Algeria [<xref ref-type="bibr" rid="ref2">2</xref>]. In Tunisia, only two cases were reported [<xref ref-type="bibr" rid="ref3">3</xref>,<xref ref-type="bibr" rid="ref4">4</xref>].</p>
<p>The primary lesion is thought to develop as a result of percutaneous traumatic inoculation [<xref ref-type="bibr" rid="ref5">5</xref>]. This is the case of our patient. Indeed, he was a victim of limb traumatism with inoculation of wood in the area of the lesion.</p>
<p>The disease affects predominantly men. Typical lesions grow slowly over many years and tend to be found on the lower limbs. The morphology of the lesion may be tumor, nodular, verrucous, plaque-like, psoriasiform, and papule as in our case or scar [<xref ref-type="bibr" rid="ref6">6</xref>].</p>
<p>In our country chromomycosis lesions may be confused with leishmaniasis, verrucous tuberculosis, and tertiary syphilis [<xref ref-type="bibr" rid="ref3">3</xref>,<xref ref-type="bibr" rid="ref4">4</xref>]. Mycologic tests are used to confirm the diagnosis. The principal causal agent is Fonsecaea pedrosoi, followed by four species in order of frequency, Phialophora verrucosa, Cladosporium carrionii, Fonsecaea compacta, and Rhinocladiella aquaspera [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref7">7</xref>].</p>
<p>Histologic appearances are hyperkeratosis, pseudoepitheliomatous hyperplasia and granulomas in the upper and mid dermis. The granulomas are mostly of tuberculoid type, although a few suppurative granulomas are present. Intraepidermal microabscesses are often present. There is a background infiltrate of chronic inflammatory cells, and sometimes a few eosinophils, in the upper dermis, round, thick-walled, golden brown cells (sclerotic bodies, muriform cells, medlar bodies) 5-12 micrometer can be seen in giant cells and lying free in the epidermal microabscesses. These sclerotic bodies are usually seen readily in heamatoxylin and eosin preparations and particularly in sections stained with hematoxylin alone [<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref5">5</xref>,<xref ref-type="bibr" rid="ref8">8</xref>].</p>
<p>If not diagnosed and treated early, chromomycosis has a chronic evolutional course. The most frequent complication was secondary bacterial infection. Chronic chromomycosis also has potential association with epidermoid carcinoma (14 cases are reported in the literature) [<xref ref-type="bibr" rid="ref8">8</xref>,<xref ref-type="bibr" rid="ref9">9</xref>] and also with skin melanoma [<xref ref-type="bibr" rid="ref10">10</xref>]. Central nervous system invasion is possible and may be fatal [<xref ref-type="bibr" rid="ref11">11</xref>].</p>
<p>Treatment in localized lesions can be surgical. Widespread lesions and long-standing cases can be treated medically [<xref ref-type="bibr" rid="ref12">12</xref>]</p>
<p>Finally, Chromomycosis is quite rare in our country. Anatomopathologists should be aware of this diagnosis.</p>
</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>