<?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>0300-9041</journal-id>
<journal-title><![CDATA[Ginecología y obstetricia de México]]></journal-title>
<abbrev-journal-title><![CDATA[Ginecol. obstet. Méx.]]></abbrev-journal-title>
<issn>0300-9041</issn>
<publisher>
<publisher-name><![CDATA[Federación Mexicana de Colegios de Obstetricia y Ginecología A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0300-90412025000500002</article-id>
<article-id pub-id-type="doi">10.24245/gom.v93i5.9364</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Angiomiofibroblastoma. Un tumor poco común. Estudio clinicopatológico de cuatro casos]]></article-title>
<article-title xml:lang="en"><![CDATA[Angiomyofibroblastoma. A rare tumor. Clinicopathological study of four cases]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sarabia Ochoa]]></surname>
<given-names><![CDATA[Rosalía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García de la Torre]]></surname>
<given-names><![CDATA[Juan Pablo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Amezcua Recover]]></surname>
<given-names><![CDATA[Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General Universitario de Albacete Servicio de anatomía patológica ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Spain</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital General Universitario de Albacete Servicio de ginecología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Spain</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2025</year>
</pub-date>
<volume>93</volume>
<numero>5</numero>
<fpage>167</fpage>
<lpage>174</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0300-90412025000500002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0300-90412025000500002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0300-90412025000500002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  OBJETIVO:  Analizar las características clínicas, histopatológicas y el tratamiento de las pacientes con angiomiofibroblastoma.  MATERIALES Y MÉTODOS:  Análisis retrospectivo y descriptivo de pacientes con diagnóstico histopatológico de angiomiofibroblastoma atendidas en el Hospital General de Albacete entre los años 2006 a 2023. Se analizaron las características clínicas, histopatológicas, el tratamiento y la evolución.  RESULTADOS:  Se analizaron 1919 biopsias vulvares y 824 vaginales. El 67.07% de las muestras correspondieron a lesiones benignas, el 19.68% a lesiones displásicas y un 13.23% a neoplasias malignas. Se identificaron cuatro casos de pacientes con diagnóstico de angiomiofibroblastoma, que representaron el 0.14% de todas las lesiones. La edad media de las pacientes fue de 41 años, con límites de 31 y 55 años. El tratamiento fue completamente quirúrgico y no se identificaron recurrencias.  CONCLUSIONES:  El angiomiofibroblastoma es una neoplasia benigna de tejidos blandos, poco común. El diagnóstico diferencial es decisivo debido a que sus manifestaciones clínicas y sus características histológicas pueden parecerse a otros tumores mesenquimatosos vulvares, pero con comportamiento biológico y pronóstico diferentes.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  OBJECTIVE:  To analyze the clinical and histopathologic characteristics and treatment of patients with angiomyofibroblastoma.  MATERIALS AND METHODS:  Retrospective and descriptive analysis of patients with a histopathologic diagnosis of angiomyofibroblastoma treated at the General Hospital of Albacete between 2006 and 2023. Clinical and histopathologic characteristics, treatment, and follow-up were analyzed.  RESULTS:  A total of 1,919 vulvar biopsies and 824 vaginal biopsies were analyzed. Benign lesions accounted for 67.07%, dysplastic lesions for 19.68%, and malignant neoplasms for 13.23% of the specimens. Four cases of patients diagnosed with angiomyofibroblastoma were identified, representing 0.14% of all lesions. The mean age of the patients was 41 years with a range of 31 to 55 years. Treatment was entirely surgical and no recurrences were observed.  CONCLUSIONS:  Angiomyofibroblastoma is a rare benign soft tissue neoplasm. Differential diagnosis is crucial because its clinical manifestations and histologic features may resemble other vulvar mesenchymal tumors, but with different biological behavior and prognosis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Angiomiofibroblastoma]]></kwd>
<kwd lng="es"><![CDATA[biopsias vulvares]]></kwd>
<kwd lng="es"><![CDATA[biopsias vaginales]]></kwd>
<kwd lng="es"><![CDATA[neoplasia benigna de partes blandas]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico diferencial]]></kwd>
<kwd lng="en"><![CDATA[Angiomyofibroblastoma]]></kwd>
<kwd lng="en"><![CDATA[Vulvar biopsies]]></kwd>
<kwd lng="en"><![CDATA[Vaginal biopsies]]></kwd>
<kwd lng="en"><![CDATA[benign soft tissue neoplasm]]></kwd>
<kwd lng="en"><![CDATA[Differential diagnosis]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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