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<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-8-354</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20173.101</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Letter to the Editor</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Cerebriform nevus sebaceous: A rare clinical variant of nevus sebaceous</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Tamer</surname>
<given-names>Funda</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Yuksel</surname>
<given-names>Mehmet Eren</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label><italic>Department of Dermatology, Ufuk University School of Medicine, Ankara, Turkey</italic></aff>
<aff id="aff2"><label>2</label><italic>Department of General Surgery, Aksaray University School of Medicine, Aksaray, Turkey</italic></aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding author:</bold> Dr. Funda Tamer, E-mail: <email xlink:href="fundatmr@yahoo.com">fundatmr@yahoo.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2017</year>
</pub-date>
<volume>8</volume>
<issue>3</issue>
<fpage>354</fpage>
<lpage>355</lpage>
<history>
<date date-type="received"><day>14</day><month>06</month><year>2016</year></date>
<date date-type="accepted"><day>06</day><month>08</month><year>2016</year></date>
</history>
<permissions>
<copyright-statement>Copyright: &#x000a9; Our Dermatol Online 3</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>A 30-year-old Caucasian female presented with a hairless plaque on her head. The patient admitted that she had this asymptomatic lesion since birth. However, the patient complained that the size of the lesion had gradually increased in the last ten years. The physical examination of the patient revealed a firm, well defined, pink-orange coloured, oval, alopecic plaque with cerebriform surface measuring 3x2 cm on the vertex (<xref ref-type="fig" rid="F1">Fig. 1</xref>). The past medical history was unremarkable. Moreover, there was no history of trauma, skeletal, neurological or ocular abnormalities. In the light of clinical findings and the history of the patient, the lesion was diagnosed as cerebriform nevus sebaceous. Because of the risk of malignant transformation, surgical excision of the lesion was advised. However, the patient refused surgical intervention. Therefore, regular follow up was recommended.</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Cerebriform nevus sebaceous. A firm, well defined, pink-orange coloured, oval, alopecic plaque with cerebriform surface measuring 3x2 cm on the scalp.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-354-g001.tif"/>
</fig>
<p>Nevus sebaceous is a rare cutaneous hamartoma which consists of sebaceous glands [<xref ref-type="bibr" rid="ref1">1</xref>]. It is usually present at birth as a yellowish-orange coloured, alopecic plaque with a smooth surface on the scalp. However, the lesion may thicken and become verrucous or nodular during adolescence [<xref ref-type="bibr" rid="ref2">2</xref>]. Although nevus sebaceous is a benign lesion, it may give rise to basal cell carcinoma, sebaceous carcinoma, apocrine carcinoma and malignant eccrine poroma. Moreover, large sebaceous nevi may be associated with neurocutaneous syndrome which is associated with neurological defects and skeletal abnormalities [<xref ref-type="bibr" rid="ref1">1</xref>].</p>
<p>Cerebriform nevus sebaceous is a very rare clinical variant of nevus sebaceous [<xref ref-type="bibr" rid="ref3">3</xref>]. It was first described by Ramesh et al. in 1988 [<xref ref-type="bibr" rid="ref4">4</xref>]. Since then, only 13 cases of cerebriform nevus sebaceous have been reported in English medical literature to the best of our knowledge [<xref ref-type="bibr" rid="ref1">1</xref>]. Hereby, we would like to share the clinical appearance of cerebriform nevus sebaceous with our colleagues (<xref ref-type="fig" rid="F1">Fig. 1</xref>)</p>
<p>Cerebriform nevus sebaceous is characterized by large, verrucous, pink, alopecic nodules with cerebriform surface [<xref ref-type="bibr" rid="ref1">1</xref>,<xref ref-type="bibr" rid="ref4">4</xref>]. The diagnosis is usually made by its clinical features, however histopathological examination is mandatory in order to reach a definitive diagnosis. It has been suggested that PTCH gene deletion and mosaic mutations in HRAS and KHAS genes might play role in development of nevus sebaceous. Nevertheless, the cause of cerebriform appearance of the lesion remains unknown [<xref ref-type="bibr" rid="ref4">4</xref>]. Seborrheic keratosis, epidermal nevus and warts should be included in the differential diagnosis of cerebriform nevus sebaceous. Surgical excision and close follow up are advised because of the risk of malignant transformation [<xref ref-type="bibr" rid="ref3">3</xref>].</p>
</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>