<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>2182-2395</journal-id>
<journal-title><![CDATA[Revista da Sociedade Portuguesa de Dermatologia e Venereologia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Soc Port Dermatol Venereol]]></abbrev-journal-title>
<issn>2182-2395</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Dermatologia e Venereologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2182-23952020000400063</article-id>
<article-id pub-id-type="doi">10.29021/spdv.78.4.1245</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Angiomatoid Spitz Nevus]]></article-title>
<article-title xml:lang="pt"><![CDATA[Nevo de Spitz Angiomatoide]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lopes]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Afonso-João]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Teixeira]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Baptista]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Centro Hospitalar de Vila Nova de Gaia/ Espinho Dermatology Department ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Portugal</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Centro Hospitalar de Vila Nova de Gaia/ Espinho Pathology Department ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Portugal</country>
</aff>
<pub-date pub-type="pub">
<day>30</day>
<month>12</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>30</day>
<month>12</month>
<year>2020</year>
</pub-date>
<volume>78</volume>
<numero>4</numero>
<fpage>63</fpage>
<lpage>65</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S2182-23952020000400063&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S2182-23952020000400063&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S2182-23952020000400063&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Angiomatoid Spitz nevus is a rare tumor that combines the classic aspects of Spitz nevus with a prominent vascular component. Clinically, it presents as a pink or brownish papule, usually solitary, in the extremities of young adults. On histology, it is characterized by a proliferation of epithelioid or spindle cell melanocytes embedded in a fibrous stroma, where a dense proliferation of small vessels is evident. The differential diagnosis with malignant melanoma can be difficult, particularly with the desmoplastic variant or with those with marked regression. Its behavior is benign, as suggested by the absence of local recurrences or distant metastases during long-term follow-up.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[RESUMO  O nevo de Spitz angiomatoide é um tumor raro que associa os aspetos clássicos do nevo de Spitz a uma componente vascular marcada. Clinicamente, manifesta-se como uma lesão papular rosada ou acastanhada, habitualmente solitária, mais frequente nas extremidades de adultos jovens. À histologia, caracteriza-se por uma proliferação de melanócitos epitelioides ou fusiformes num estroma fibroso denso, onde é evidente uma assinalável proliferação de pequenos vasos. O diagnóstico diferencial com melanoma maligno pode ser difícil, particularmente com a variante desmoplásica ou com aqueles com aspetos de regressão. O seu comportamento é benigno, comprovado pela ausência de recidivas locais ou metástases à distância durante o seguimento a longo prazo.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Neoplasias da Pele]]></kwd>
<kwd lng="pt"><![CDATA[Nevo de Células Epitelioides e Fusiformes.]]></kwd>
<kwd lng="en"><![CDATA[Nevus, Epithelioid and Spindle Cell]]></kwd>
<kwd lng="en"><![CDATA[Skin Neoplasms]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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