<?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>2444-054X</journal-id>
<journal-title><![CDATA[Cirugía y cirujanos]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. cir.]]></abbrev-journal-title>
<issn>2444-054X</issn>
<publisher>
<publisher-name><![CDATA[Academia Mexicana de Cirugía A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2444-054X2024000600018</article-id>
<article-id pub-id-type="doi">10.24875/ciru.22000220</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Solitary fibrous tumor of the abdominal wall: a new case with literature review]]></article-title>
<article-title xml:lang="es"><![CDATA[Tumor fibroso solitario de la pared abdominal: un nuevo caso con revisión de la literatura]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz-Juliá]]></surname>
<given-names><![CDATA[María L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz-Luque]]></surname>
<given-names><![CDATA[Virgilio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ariza-Estepa]]></surname>
<given-names><![CDATA[Macarena]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Díaz-Roldán]]></surname>
<given-names><![CDATA[Jorge]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Parra-Membrives]]></surname>
<given-names><![CDATA[Pablo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Valme University Hospital Department of General and Digestive Surgery ]]></institution>
<addr-line><![CDATA[Seville ]]></addr-line>
<country>Spain</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Valme University Hospital Department of Pathology ]]></institution>
<addr-line><![CDATA[Seville ]]></addr-line>
<country>Spain</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2024</year>
</pub-date>
<volume>92</volume>
<numero>6</numero>
<fpage>823</fpage>
<lpage>828</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2444-054X2024000600018&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2444-054X2024000600018&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2444-054X2024000600018&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Objective: We present a solitary fibrous tumor (SFT) of the abdominal wall treated laparoscopically.  Method: We will discuss the clinicopathologic characteristics and will present a review of the literature.  Results: SFTs are rare neoplasms of mesenchymal origin. Its location in the abdominal wall is extremely rare. To the best of our knowledge, only 20 cases have currently been described in the literature.  Conclusions: Complete surgical resection is the main therapy for all cases. A laparoscopic approach is safe. Clinical-radiological follow-up must be carried out due to its uncertain behavior, and perioperative treatment may be necessary in high-risk patients.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Objetivo: Presentamos un caso de tumor fibroso solitario de pared abdominal tratado por vía laparoscópica.  Método: Se discuten las características clinicopatológicas y se presenta una revisión de la literatura.  Resultados: Los tumores fibrosos solitarios son neoplasias raras de origen mesenquimatoso. Su localización en la pared abdominal es extremadamente rara. Hasta donde sabemos, solo se han descrito 20 casos en la literatura.  Conclusiones: La resección quirúrgica completa es la terapia principal para todos los casos. El abordaje laparoscópico es seguro. Debe realizarse un seguimiento clínico-radiológico debido a su comportamiento incierto, pudiendo ser necesario un tratamiento perioperatorio en pacientes de alto riesgo.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Extrapleural solitary fibrous tumor]]></kwd>
<kwd lng="en"><![CDATA[Solitary fibrous tumor]]></kwd>
<kwd lng="en"><![CDATA[Mesenchymal neoplasm]]></kwd>
<kwd lng="es"><![CDATA[Tumor fibroso solitario extrapleural]]></kwd>
<kwd lng="es"><![CDATA[Tumor fibroso solitario]]></kwd>
<kwd lng="es"><![CDATA[Neoplasia mesenquimatosa]]></kwd>
</kwd-group>
</article-meta>
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