<!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-8-231</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20172.64</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Letter to the Editor</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Dubreuilh&#x2019;s melanosis or malignant lentigo</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"/>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bouhajja</surname>
<given-names>Leila</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Goucha</surname>
<given-names>Aida</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rekik</surname>
<given-names>Wafa</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>May</surname>
<given-names>Ahmed El</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gamoudi</surname>
<given-names>Amor</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
</contrib-group>
<aff id="aff1"><italic>Department of Pathology, Carcinological Institute Salah Azaiez, 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>2</issue>
<fpage>231</fpage>
<lpage>232</lpage>
<history>
<date date-type="received"><day>08</day><month>03</month><year>2016</year></date>
<date date-type="accepted"><day>05</day><month>06</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>
</article-meta>
</front>
<body>
<sec>
<title/>
<p>Sir,</p>
<p>We report a 69 year-old man who presented with a 5-year history of pigmented lesion on the tip of the nose. Physical examination revealed a 2 cm, hyperpigmented lesion of the nose. The cervical and abdominal ultrasonographies were normal. A surgical resection of the tumor was performed. Grossly, the tumor was flat, black or dark brown, and measured 1.5 cm of diameter. Histological examination showed a confluent growth of melanocytes along dermo-epidermal junction with involvement of adnexal structures (<xref ref-type="fig" rid="F1">Fig. 1</xref>). Some isolated or nested cells infiltrated papillary dermis and were surrounded by inflammatory and fibrous stroma (<xref ref-type="fig" rid="F2">Fig. 2</xref>). The derm presented a significant solar elastosis and the epidermis was atrophic. These features confirmed the diagnosis of Dubreuilh&#x2019;s melanosis. At 3 years of follow-up, the patient was asymptomatic and there was no recurrence.</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Confluent growth of melanocytes along dermo-epidermal junction with involvement of adnexal structures.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-231-g001.tif"/>
</fig>
<fig id="F2">
<label>Figure 2</label>
<caption>
<p>Some isolated or nested cells infiltrated papillary dermis and were surrounded by inflammatory and fibrous stroma.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-231-g002.tif"/>
</fig>
<p>The patient&#x2019;s informed consent was obtained.</p>
<p>Prior to the study, patient gave written consent to the examination and biopsy after having been informed about the procedure.</p>
<p>Lentigo maligna (LM) is a premalignant melanocytic neoplasm occurring on the sun-exposed skin of the old patient (&#x003E;60 ans) [<xref ref-type="bibr" rid="ref1">1</xref>]. It&#x2019;s a subtype of melanoma in situ, and it has a female preponderance. Lentigo maligna melanoma (LMM) is one of the four main subtypes of invasive melanoma and represents 5-15&#x0025; of cases [<xref ref-type="bibr" rid="ref2">2</xref>]. Clinically, it&#x2018;s a pigmented macula that is dark brown, tan, or black, located on the face or on the scalp [<xref ref-type="bibr" rid="ref3">3</xref>]. The clinical differential diagnoses are a simple solar lentigo, a pigmented actinic keratosis and seborrheic keratosis. Histological image of LM is that of a melanoma in situ. LMM shows a dermal infiltrate of atypical melanocytes [<xref ref-type="bibr" rid="ref4">4</xref>]. Immunohistochemistry, the melanocytes are positive for Melan-A antigen and HMB45. Furthermore, epidemiological and molecular studies differentiate two lanes of carcinogenesis for melanoma: A way for the young adults, with many nevi and having an intense and intermittent sun exposure, and a second, like the LMM, older individuals who are chronically exposed to sun. Molecular analyzes seem to support this duality by highlighting the BRAF mutations in the first group melanoma [<xref ref-type="bibr" rid="ref5">5</xref>]. Surgical excision is the treatment of choice to obtain clinical and histologic clearance. The recurrence rate after micrographic surgery is about 4-5&#x0025; and 7-10&#x0025; after conventional surgery (cryotherapy and radiotherapy) [<xref ref-type="bibr" rid="ref1">1</xref>]. A 5 millimeter cutaneous margin must be resected around this lesion. LM prognosis is excellent as an in situ (100&#x0025;) but LMM prognosis depends on tumor thickness (Breslow index).</p>
</sec>
<sec id="sec1-2" sec-type="conclusion">
<title>CONCLUSION</title>
<p>LM and LMM differ from other types of melanoma, by their clinical, histological features, carcinogenesis, evolution and require appropriate care.</p>
<sec id="sec2-1">
<title>Consent</title>
<p>The examination of the patient was conducted according to the Declaration of Helsinki principles. Written informed consent was obtained from the patient for publication of this article.</p>
</sec>
</sec>
</body>
<back>
<ref-list>
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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>
