<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "JATS-journalpublishing1.dtd"><article xml:lang="KO" article-type="case-report">

<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Korean J Gynecol Oncol Colposc</journal-id>
<journal-id journal-id-type="publisher-id">KJGOC</journal-id>
<journal-title-group>
<journal-title>Korean Journal of Gynecologic Oncology and Colposcopy</journal-title>
</journal-title-group>
<issn pub-type="ppub">0300-4015</issn>
<publisher>
<publisher-name>Korean Society of Gynecologic Oncology and Colposcopy</publisher-name>
</publisher>
</journal-meta>

<article-meta>
<article-id pub-id-type="doi">10.3802/kjgoc.2002.13.4.353</article-id>
<article-categories>
<subj-group>
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>A Case of Uterine Leiomyomas in both Rudimentary Uterine Horns in a Woman with the Mayer-Rokitansky-Kuster-Hauser Syndrome</article-title>
</title-group>

<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Lee</surname>
<given-names>Bok</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>Young Nam</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jeong</surname>
<given-names>Dae Hoon</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sung</surname>
<given-names>Moon Soo</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>Ki Tae</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>
</contrib-group>

<aff id="A1">Department of Obstetrics and Gynecology, Busan Paik Hospital, College of Medicine, InJe University, Busan, <country>Korea</country>.</aff>

<pub-date pub-type="ppub">
<month>12</month>
<year>2002</year>
</pub-date>
<pub-date pub-type="epub">
<day>12</day>
<month>03</month>
<year>2019</year>
</pub-date>
<volume>13</volume>
<issue>4</issue>
<fpage>353</fpage>
<lpage>356</lpage>

<permissions>
<copyright-statement>Copyright &#x00A9; Korean Society of Gynecologic Oncology and Colposcopy</copyright-statement>
<copyright-year>2002</copyright-year>
</permissions>

<abstract>
<p>Mayer-Rokitansky-Kuster-Hauser syndrome occurs in only approximately 1 in 4000-5000 female births. Leiomyoma is a rather common occurrence in the normal uterus, but extremely rare in mullerian remnants. Leiomyoma should be considered low on the list of differential diagnosis of pelvic mass in women with Mayer-Rokitansky-Kuster-Hauser syndrome. We have experienced a case of Mayer-Rokitansky-Kuster-Hauser syndrome associated with leiomyomas arising from both rudimentary uterine horns and report it with a brief review of literatures.</p>
</abstract>

<kwd-group>
<kwd>Mayer-Rokitansky-Kuster-Hauser syndrome</kwd>
<kwd>Leiomyoma</kwd>
</kwd-group>

</article-meta>
</front>
</article>