<?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>2221-2434</journal-id>
<journal-title><![CDATA[Revista Finlay]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Finlay]]></abbrev-journal-title>
<issn>2221-2434</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Cienfuegos. Centro Provincial de información de Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2221-24342020000100050</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Nevus verrugoso gigante con componente angiomatoso cavernoso. Presentación de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Giant Warty Nevus with Cavernous Angioma Component. Case Presentation]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez Hidalgo]]></surname>
<given-names><![CDATA[María del Rosario]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Valdés Madrigal]]></surname>
<given-names><![CDATA[Idalmis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
<xref ref-type="aff" rid="A a"/>
<xref ref-type="aff" rid="A1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Borges Sánchez.]]></surname>
<given-names><![CDATA[Eduardo Carlos]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Pediátrico General Luis Ángel Milanés Tamayo  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital General Provincial Carlos Manuel de Céspedes  ]]></institution>
<addr-line><![CDATA[Granma ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2020</year>
</pub-date>
<volume>10</volume>
<numero>1</numero>
<fpage>50</fpage>
<lpage>55</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S2221-24342020000100050&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S2221-24342020000100050&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S2221-24342020000100050&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El nevus verrugoso es una hiperplasia benigna y congénita de la epidermis superficial y los anexos. Se considera un hamartoma derivado del ectodermo, posiblemente ocasionado por una aberración cromosómica localizada en el brazo largo del cromosoma 1. Se presenta el caso de un paciente de sexo masculino, de 3 años de edad, portador de nevus verrugoso gigante con componente angiomatoso cavernoso, en región occipital, sin otras anomalías. Se utilizaron los datos provenientes de fuentes documentales (carné obstétrico, carné pediátrico, historias clínicas hospitalaria y ambulatoria), exámenes de laboratorio e imagenológicos, así como información obtenida a partir de la entrevista a la madre, para describir la evolución desde el nacimiento. Se realizó búsqueda bibliográfica y se comentan aspectos relacionados con la incidencia, localizaciones, edad de presentación, las características clínicas e histopatológicas, el tratamiento y la evolución. Se realiza este reporte por la baja frecuencia de esta patología en el Hospital Pediátrico General Luis Ángel Milanés de Bayamo, Granma.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT The warty nevus is a benign and congenital hyperplasia of the superficial epidermis and the annexes. It is considered a hamartoma derived from the ectoderm, possibly caused by a chromosomal aberration located on the long arm of chromosome 1.The case of a 3 year-old male patient is presented, with a giant warty nevus with an angioma cavernous component in the occipital region, without other anomalies. Data from documentary sources (such as obstetric card, pediatric card and hospital and outpatient medical records), laboratory and imaging tests, as well as information obtained from the mother's interview, were used to describe the evolution from birth. Issues related to the incidence, locations, age of presentation, clinical and histopathological characteristics, treatment and evolution are discussed, on the bases of a bibliographic search. This report is made due to the low frequency of this pathology at the Paquito González Cueto de Cienfuegos University Pediatric Hospital.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[hiperplasia benigna]]></kwd>
<kwd lng="es"><![CDATA[aberraciones cromosómicas]]></kwd>
<kwd lng="es"><![CDATA[reporte de caso]]></kwd>
<kwd lng="en"><![CDATA[benign hyperplasia]]></kwd>
<kwd lng="en"><![CDATA[chromosomal aberration]]></kwd>
<kwd lng="en"><![CDATA[case reports]]></kwd>
</kwd-group>
</article-meta>
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