<?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>2795-5001</journal-id>
<journal-title><![CDATA[Portuguese Journal of Dermatology and Venereology]]></journal-title>
<abbrev-journal-title><![CDATA[Port J Dermatol Venereol.]]></abbrev-journal-title>
<issn>2795-5001</issn>
<publisher>
<publisher-name><![CDATA[Permanyer Publications]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2795-50012025000100052</article-id>
<article-id pub-id-type="doi">10.24875/pjdv.24000079</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Abrikossoff tumor: rare dermatosis in a case with epidemiological and therapeutic specificities]]></article-title>
<article-title xml:lang="pt"><![CDATA[Tumor de Abrikossoff: dermatose rara em caso com especificidades epidemiológicas e terapêuticas]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cruz]]></surname>
<given-names><![CDATA[Carolina D.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernandes]]></surname>
<given-names><![CDATA[Elizabeth L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cunha]]></surname>
<given-names><![CDATA[Sergio F. de S.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Beltrão]]></surname>
<given-names><![CDATA[Adriana R.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pessanha]]></surname>
<given-names><![CDATA[André C.A.F.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Mogi das Cruzes University Dermatology Department ]]></institution>
<addr-line><![CDATA[SP ]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,UNITAU Dermoscopy Department ]]></institution>
<addr-line><![CDATA[SP ]]></addr-line>
<country>Brazil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2025</year>
</pub-date>
<volume>83</volume>
<numero>1</numero>
<fpage>52</fpage>
<lpage>55</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S2795-50012025000100052&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S2795-50012025000100052&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S2795-50012025000100052&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Granular cell tumor is a rare benign neoplasm, which preferentially affects the oral cavity, more common in adults and rare in children. This report is about a 9-year-old patient with a painful periungual nodule of the fifth finger of the right hand, with two years of evolution. The anatomopathological examination revealed an Abrikossoff tumor, without bone involvement on X-ray and positive markers on immunohistochemistry. Due to the location of the lesion, Mohs micrographic surgery was chosen in order to have greater tissue preservation and local functionality. There was no recurrence of the tumor, with resolutive surgery and satisfactory aesthetic results.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo O tumor de células granulares é uma neoplasia benigna rara, que afeta preferencialmente a cavidade oral, mais comum em adultos e rara em crianças. Este relato trata de paciente de 9 anos com história de nodulação periungueal dolorosa do quinto dedo da mão direita, com dois anos de evolução. O exame anatomopatológico revelou tumor de Abrikossoff, sem envolvimento ósseo na radiografia e marcadores positivos na imunohistoquímica. Devido à localização da lesão, optou-se pela cirurgia micrográfica de Mohs, para maior preservação tecidual e funcionalidade local. Não houve recidiva do tumor, com cirurgia resolutiva e resultado estético satisfatório.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Mohs surgery]]></kwd>
<kwd lng="en"><![CDATA[Granular cell tumor]]></kwd>
<kwd lng="en"><![CDATA[S100 proteins]]></kwd>
<kwd lng="en"><![CDATA[Abrikossoff tumor]]></kwd>
<kwd lng="pt"><![CDATA[Cirurgia de mohs]]></kwd>
<kwd lng="pt"><![CDATA[Tumor de células granulares]]></kwd>
<kwd lng="pt"><![CDATA[Proteína s100]]></kwd>
<kwd lng="pt"><![CDATA[Tumor de abrikossoff]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dupin]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Carlotti]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Baran]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Moulonguet]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Abrikossof granular cell tumor at the nail unit:an exceptional location]]></article-title>
<source><![CDATA[Ann Dermatol Venereol]]></source>
<year>2021</year>
<volume>148</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>195-7</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stemm]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Suster]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Wakely Jr]]></surname>
<given-names><![CDATA[PE]]></given-names>
</name>
<name>
<surname><![CDATA[Suster]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Typical and atypical granular cell tumors of soft tissue:a clinicopathologic study of 50 patients]]></article-title>
<source><![CDATA[Am J Clin Pathol]]></source>
<year>2017</year>
<volume>148</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>161-6</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Olayiwola]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Hook]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Miller]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Maguiness]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Cutaneous granular cell tumors in children:case series and review of the literature]]></article-title>
<source><![CDATA[Pediatr Dermatol]]></source>
<year>2017</year>
<volume>34</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>e187-90</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kim]]></surname>
<given-names><![CDATA[HJ]]></given-names>
</name>
<name>
<surname><![CDATA[Lee]]></surname>
<given-names><![CDATA[MG]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Granular cell tumors on unusual anatomic locations]]></article-title>
<source><![CDATA[Yonsei Med J]]></source>
<year>2015</year>
<volume>56</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>1731</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
