<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.3 20070202//EN" "journalpublishing.dtd">
<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-8-197</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20172.53</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Cerebriform intradermal nevus - A rare clinical entity presenting as cutis verticis gyrata</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Kudligi</surname>
<given-names>Chandramohan</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kuntoji</surname>
<given-names>Vidya</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bhagwat</surname>
<given-names>Pradeep Vittal</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mohanbhai</surname>
<given-names>Chovatiya Keyur</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tazeen</surname>
<given-names>Safura</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
</contrib-group>
<aff id="aff1"><italic>Department of Dermatology and Venereology, Karnataka Institute of Medical Sciences, Hubli, Karnataka, India</italic></aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding author:</bold> Dr. Vidya Kuntoji, E-mail: <email xlink:href="drvidyakuntoji@gmail.com">drvidyakuntoji@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2017</year>
</pub-date>
<volume>8</volume>
<issue>2</issue>
<fpage>197</fpage>
<lpage>199</lpage>
<history>
<date date-type="received"><day>10</day><month>09</month><year>2016</year></date>
<date date-type="accepted"><day>21</day><month>10</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>Cutis verticis gyrata is a rare skin condition characterized by convoluted folds and furrows formed from thickened skin resembling a cerebriform pattern. The condition is usually but not exclusively limited to the scalp. It may present in either primary form with or without any associations or in secondary forms with a wide variety of causes. Cerebriform intradermal nevus is one such rare cause of this unusual condition. We present a case of cerebriform intradermal nevus involving scalp and the upper half of left cheek which had both cerebriform appearances as well as the smooth surface.</p>
</abstract>
<kwd-group>
<kwd>Cutis verticis gyrata</kwd>
<kwd>Intradermal</kwd>
<kwd>Nevus</kwd>
<kwd>Scalp</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="sec1-1" sec-type="intro">
<title>INTRODUCTION</title>
<p>Cutis verticis gyrata is a rare disorder of the scalp, characterized by the formation of furrows and folds resembling the surface of the brain [<xref ref-type="bibr" rid="ref1">1</xref>]. Though it is mainly seen on the scalp, it can also be located on the neck, legs, buttocks, scrotum or back [<xref ref-type="bibr" rid="ref2">2</xref>]. It can be classified into primary and secondary types. The former can be either essential or non-essential depending on the presence of associations like cerebral palsy, epilepsy, seizure, mental retardation and the latter is caused by a wide variety of underlying conditions. Cerebriform intradermal nevus, a rare condition of the scalp is one such cause of cutis verticis gyrate [<xref ref-type="bibr" rid="ref3">3</xref>,<xref ref-type="bibr" rid="ref4">4</xref>].</p>
</sec>
<sec id="sec1-2" sec-type="cases">
<title>CASE REPORT</title>
<p>A 28-year-old female presented to our Dermatology outpatient department with a swelling/mass on one-half of the scalp which was present since birth and was gradually progressive. It was associated with occasional mild itching. The patient also gave the history of hair loss/alopecia in the area of swelling since birth. She was born out of a non-consanguineous marriage with an uneventful birth history. The family history was insignificant and her elder sister was normal. There was no history of epilepsy or mental retardation. On cutaneous examination, there was a 25&#215;15cm mass, which was confined to left half of the scalp involving left temporal and left occipital regions and a part of it was extending to upper half of left cheek abutting the left eye (<xref ref-type="fig" rid="F1">Fig. 1</xref>). It was non-tender and soft to firm in consistency. There were deep folds in the lowermost part of the swelling in parietal and occipital regions. There were mild scaling and atrophy of skin along with alopecia over the swelling. The skin over the swelling was not pinchable.</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Mass having both convoluted and smooth surface involving left half of the scalp.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-197-g001.tif"/>
</fig>
<p>Routine blood investigations were normal. Ophthalmological examination was normal. CT scan of the head showed no bony or intracranial abnormalities. Histopathological examination of punch biopsy specimens revealed nests of nevus cells containing varying amounts of melanin in the papillary and reticular dermis without any cellular atypia (Figs. <xref ref-type="fig" rid="F2">2</xref> and <xref ref-type="fig" rid="F3">3</xref>). The diagnosis was consistent with Cerebriform intradermal nevus.</p>
<fig id="F2">
<label>Figure 2</label>
<caption>
<p>Skin biopsy involving nests of naevus cells surrounded by thick collagen bundles in the dermis (H&#x0026;E: &#215;10).</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-197-g002.tif"/>
</fig>
<fig id="F3">
<label>Figure 3</label>
<caption>
<p>Skin biopsy showing melanin pigment and naevus cells (H&#x0026;E: &#215;40).</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-8-197-g003.tif"/>
</fig>
</sec>
<sec id="sec1-3" sec-type="discussion">
<title>DISCUSSION</title>
<p>Cutis verticis gyrata is an abnormality of the scalp characterized by the formation of furrows and folds resembling the surface of the brain. It is classified as primary and secondary types. The primary form is further classified as essential and non-essential types. The primary essential form has no other associations with it whereas the primary non-essential type is often associated with seizure, mental retardation, cataracts and optic atrophy. The secondary form is caused due to underlying diseases like acromegaly, amyloidosis, cylindroma, focal mucinosis, myxedema, melanocytic nevi, neurofibroma, pachydermoperiostosis, tuberous sclerosis, turner syndrome and so on [<xref ref-type="bibr" rid="ref5">5</xref>]. Cerebriform intradermal nevus is one such rare cause of secondary cutis verticis gyrata which confers a convoluted appearance.</p>
<p>It is a nodular nevus cerebriform on its surface and is present in the dermis on histopathology [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref7">7</xref>]. Hammond and Ransom first described a Cerebriform nevus resembling cutis verticis gyrata in 1937 [<xref ref-type="bibr" rid="ref8">8</xref>]. Presenting at birth or early life, it is attributed that females are more likely to develop this condition [<xref ref-type="bibr" rid="ref7">7</xref>]. It can be either asymptomatic or can be associated with progressive alopecia, pruritus, tenderness, burning, bleeding and fetid odor [<xref ref-type="bibr" rid="ref9">9</xref>,<xref ref-type="bibr" rid="ref10">10</xref>]. Our patient was female and had mild occasional itching and also alopecia confined to the nevus since birth. Unlike the reports in the literature [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref11">11</xref>,<xref ref-type="bibr" rid="ref12">12</xref>], our patient had limited convolutions with a major part of the surface of the scalp being plain. And its extension on the face involving half of the upper cheek was unusual in this case. Although there is varied opinion regarding the relation of giant melanocytic naevus with the cerebral intradermal nevus, the possibility of giant melanocytic naevus in our case was ruled out by the absence of hairy and junctional activity [<xref ref-type="bibr" rid="ref7">7</xref>,<xref ref-type="bibr" rid="ref13">13</xref>]. Our patient was normal in intellect and she did not have any other abnormalities. But it is important to know that cerebriform intradermal nevus is associated with the risk of malignant melanoma [<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref15">15</xref>]. The life-time incidence of melanoma arising in a giant nevus or in smaller nevi is 6.3&#x0025; and 12&#x0025; [<xref ref-type="bibr" rid="ref9">9</xref>].</p>
</sec>
<sec id="sec1-4" sec-type="conclusion">
<title>CONCLUSION</title>
<p>Cerebriform intradermal nevus is one of the rare causes of Cutis verticis gyrata. Apart from its cerebriform appearance, the major part of the surface of scalp was smooth and also it had an extension over the face. Since it carries the risk of malignant melanoma, there lies the importance of early diagnosis, regular follow-up and management of this rare condition.</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>
