<?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>1405-0099</journal-id>
<journal-title><![CDATA[Cirujano general]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. gen]]></abbrev-journal-title>
<issn>1405-0099</issn>
<publisher>
<publisher-name><![CDATA[Asociación Mexicana de Cirugía General A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-00992021000200137</article-id>
<article-id pub-id-type="doi">10.35366/106726</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Hernia inguinal derecha con presencia de útero, trompa de Falopio y ovario, asociada a síndrome de Mayer-Rokitansky-Küster-Hauser]]></article-title>
<article-title xml:lang="en"><![CDATA[Right inguinal hernia with the presence of uterus, falopian tube and ovary associated with Mayer-Rokitansky-Küster-Hauser syndrome]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ramírez-Mendoza]]></surname>
<given-names><![CDATA[Carlos Humberto]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez-Sierra]]></surname>
<given-names><![CDATA[Luis Enrique]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Romero-Lanza]]></surname>
<given-names><![CDATA[Ana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chicas Reyes]]></surname>
<given-names><![CDATA[Araceli]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Hondureño de Seguridad Social  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Honduras</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Hondureño de Seguridad Social  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Honduras</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Instituto Hondureño de Seguridad Social  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Honduras</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Instituto Hondureño de Seguridad Social  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Honduras</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2021</year>
</pub-date>
<volume>43</volume>
<numero>2</numero>
<fpage>137</fpage>
<lpage>140</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-00992021000200137&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-00992021000200137&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-00992021000200137&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  La hernia de pared abdominal es una patología frecuente, se calcula que la prevalencia es cercana a 5% en la población general; la presentación más frecuente es de tipo inguinal, cerca de 70% del total. El síndrome de Mayer-Rokitansky-Küster-Hauser es una rara anomalía congénita del tracto genital, se desconoce su etiología. Por lo general se presenta como amenorrea primaria en mujeres adolescentes, con genitales externos y crecimiento normales. Puede asociar otras alteraciones, especialmente a nivel genitourinario.  Caso clínico:  Paciente femenino de 25 años de edad, con antecedente patológico de amenorrea primaria y antecedente quirúrgico de hernioplastía inguinal izquierda, con historia de protrusión en región inguinal derecha de tres años de evolución, que aumenta al realizar esfuerzo físico. Al examen físico se observó protrusión en región inguinal derecha aproximadamente de 5 cm de diámetro con Valsalva, sin cambios de color o inflamatorios, a la auscultación presentó ruidos intestinales normales, a la palpación se detectó masa en fosa iliaca derecha de consistencia blanda, depresible, dolorosa, y reducible. En el examen ginecológico, paciente con fenotipo femenino y características sexuales secundarias normales presentó labios mayores y menores simétricos, conducto vaginal permeable. El diagnóstico clínico fue hernia inguinal derecha no complicada, se decidió tratamiento quirúrgico, y se programó para cirugía electiva encontrando hernia inguinal derecha, saco herniario que contiene el útero, trompa de Falopio y ovario ipsilateral.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  Abdominal wall hernia is a frequent pathology, it is estimated that the prevalence is close to 5% in the general population; the most frequent presentation is of the inguinal type, close to 70% of the total. Mayer-Rokitansky-Küster-Hauser syndrome is a rare congenital anomaly of the genital tract, its etiology is unknown. It generally presents as primary amenorrhea in adolescent women, with normal external genitalia and growth. It can associate other alterations, especially at the genitourinary level.  Clinical case:  A 25-year-old female patient, with a pathological history of primary amenorrhea and a surgical history of left inguinal hernioplasty, with a history of protrusion in the right inguinal region of three years of evolution, exacerbated by physical exertion. On physical examination, a protrusion was observed in the right inguinal region approximately 5 cm in diameter with Valsalva, without color or inflammatory changes, on auscultation he presented normal bowel sounds, on palpation he presented a mass in the right iliac fossa of a soft, depressible consistency, painful, reducible. In the gynecological examination, a patient with a female phenotype and normal secondary sexual characteristics presented symmetrical labia majora and minora, a patent vaginal canal. The clinical diagnosis was uncomplicated right inguinal hernia, surgical treatment was decided, for which elective surgery was scheduled. The postoperative diagnosis was right inguinal hernia with the presence of uterus, fallopian tube and ipsilateral ovary plus Mayer-Rokitansky-Küster-Hauser syndrome.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Hernia inguinal]]></kwd>
<kwd lng="es"><![CDATA[síndrome Mayer-Rokitansky-Küster-Hauser]]></kwd>
<kwd lng="es"><![CDATA[trompa falopio]]></kwd>
<kwd lng="es"><![CDATA[ovario]]></kwd>
<kwd lng="en"><![CDATA[Inguinal hernia]]></kwd>
<kwd lng="en"><![CDATA[Mayer-Rokitansky-Küster-Hauser syndrome]]></kwd>
<kwd lng="en"><![CDATA[falopian tube]]></kwd>
<kwd lng="en"><![CDATA[ovary]]></kwd>
</kwd-group>
</article-meta>
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