<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2017.77076</article-id><article-id pub-id-type="publisher-id">OJOG-77989</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Rupture of a Rudimentary Uterine Horn: A Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kouamé</surname><given-names>Arthur Didier</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adjoby</surname><given-names>Cassou Roland</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Konan</surname><given-names>Joachim</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Effoh</surname><given-names>N’Drin Dénis</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kakou</surname><given-names>Charles</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Diomandé</surname><given-names>Fatoumata Alice</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Koffi</surname><given-names>Soh Victor</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kouakou</surname><given-names>Firmin</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Obstetrics and Gynaecology Department of the University Hospital of Cocody-Abidjan, Abidjan, C&amp;amp;ocirc;te D’Ivoire</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>arthur.kouame@mail.huji.ac.il(KAD)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>01</day><month>07</month><year>2017</year></pub-date><volume>07</volume><issue>07</issue><fpage>748</fpage><lpage>752</lpage><history><date date-type="received"><day>May</day>	<month>17,</month>	<year>2017</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>July</month>	<year>24,</year>	</date><date date-type="accepted"><day>July</day>	<month>27,</month>	<year>2017</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Pregnancy in an abnormal uterus is a high-risk situation in obstetrics. Uterus bicornis unicollis with a rudimentary horn is often discovered incidentally. The aim of this report is to warn obstetricians about recurrent abdominal pain in the second trimester of pregnancy without any cause identified. Pregnancy can proceed in the rudimentary horn. We presented a case of a rupture of the rudimentary horn which occurred at 25 weeks of amenorrhea in an unmarried 19-year-old primigravida. The rudimentary horn was removed after performing an emergency laparotomy for an intraperitoneal hemorrhage with signs of shock. This abnormality is often revealed by uterine rupture, which usually occurs in the second trimester of pregnancy. Conclusion: We emphasize the importance of early diagnosis of this uterine abnormality, before pregnancy if possible. Undiagnosed, this condition evolves towards uterine rupture during pregnancy and requires emergency surgery with excision of the rudimentary horn.
 
</p></abstract><kwd-group><kwd>Uterine Rupture</kwd><kwd> Abdominal Pregnancy</kwd><kwd> Uterus Bicornis</kwd><kwd> Rudimentary Uterine Horn</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The embryology of uterus bicornis with a rudimentary horn is a consequence of the failure of progression of one of the two M&#252;llerian ducts between the sixth and ninth week of gestation. This rudimentary horn may have a cavity with endometrial lining of the uterus, and thus can serve as a site of implantation during pregnancy [<xref ref-type="bibr" rid="scirp.77989-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.77989-ref2">2</xref>] . Pregnancy in a rudimentary horn usually results in its rupture which can lead to a life-threatening heavy bleeding. That is an extremely rare condition 10-fold less common than abdominal pregnancy [<xref ref-type="bibr" rid="scirp.77989-ref3">3</xref>] . We describe a clinical case of a rupture of the rudimentary horn which occurred at 25 weeks of amenorrhea.</p></sec><sec id="s2"><title>2. Observation</title><p>An unmarried 19-year-old primigravida was referred to our service for persistent abdominal and pelvic pain. During this pregnancy, she had never attended any antenatal care service. Clinical examination showed a stable gene- ral condition with blood pressure 100/60 mm Hg and pulse at 88 beats/min. The abdomen was slightly distended and sensitive with dullness in both flanks. Vaginal examination disclosed a single softened closed cervix without bleeding. The first ultrasound examination was performed and suspected an abdominal pregnancy of 25 weeks with fetal death. There were no signs of peritoneal effusion. During hospitalization, she presented peritoneal effusion syndrome with signs of shock. The patient was taken for emergent laparotomy, which revealed 300 ml of blood and a deceased but morphologically normal fetus weighing 610 free in the abdominal cavity. After inspection, we discovered a rupture of the upper surface of a rudimentary left horn of a uterus bicornis unicollis. The left fallopian tube and the left ovary appeared normal and were connected on this rudimentary horn. The rudimentary horn was removed by clamping, ligating and cutting its attachment to the right horn. The postoperative course was uneventful and the patient was able to leave the hospital on post-operative day 7 (<xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>).</p></sec><sec id="s3"><title>3. Discussion</title><p>Mauriceau described the first case of uterine rupture during pregnancy in a rudimentary horn in 1669 [<xref ref-type="bibr" rid="scirp.77989-ref4">4</xref>] . This report is the first case documented in our department at the Teaching Hospital of Cocody. According to 47 studies of 570,000 women, the incidence of uterine malformations is 0.5%, and of these, 5% are horned uterus [<xref ref-type="bibr" rid="scirp.77989-ref1">1</xref>] . The incidence of rudimentary horn pregnancy is estimated at 1/100,000 to 1/140,000 [<xref ref-type="bibr" rid="scirp.77989-ref2">2</xref>] . Ten percent of these rudimentary horns</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Photo showing the uterine rupture with a dead fetus</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/9-1431425x2.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Photo showing the 2 horns of the uterus with the 2 ovaries. The ruptured horn is at the left side of the photo</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/9-1431425x3.png"/></fig><p>communicate with the main uterine horn and 35% have a cavity [<xref ref-type="bibr" rid="scirp.77989-ref1">1</xref>] . There is a slight predominance of the rudimentary horn at the right side potentially related to the more caudal location of the left M&#252;llerian duct [<xref ref-type="bibr" rid="scirp.77989-ref4">4</xref>] . The implantation of the egg in the aplastic horn is usually the result of transperitoneal migration of a spermatozoid to the rudimentary horn. Since the elasticity of the horn is limited, the risk of its rupture during pregnancy is high. This can occur early in the second trimester [<xref ref-type="bibr" rid="scirp.77989-ref5">5</xref>] .</p><p>Diagnosis of pregnancy in a uterine horn is difficult owing to the non-specific nature of the symptoms, mainly severe abdominal pain in the second trimester. The differential diagnosis might include ectopic, corneal or isthmic pregnancy [<xref ref-type="bibr" rid="scirp.77989-ref6">6</xref>] . It is associated with intraperitoneal hemorrhage, which can be revealed by ultrasound examination. Rupture frequently leads to emergency surgery, at which point a diagnosis is typically established [<xref ref-type="bibr" rid="scirp.77989-ref7">7</xref>] . Laparoscopy may be a reasonable approach in uncertain circumstances. Earlier detection of uterine malformations by ultrasound or magnetic resonance imaging (MRI) examination may be useful to prevent this devastating obstetrical accident which can lead to maternal mortality [<xref ref-type="bibr" rid="scirp.77989-ref8">8</xref>] .</p><p>When uterus bicornis with rudimentary horn is discovered incidentally without pregnancy, the rudimentary horn should be excised when possible. This procedure can be performed using a laparoscopic approach [<xref ref-type="bibr" rid="scirp.77989-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.77989-ref10">10</xref>] . If pregnancy in a rudimentary horn is diagnosed in the first trimester, it may be reasonable to continue the pregnancy with ultrasound monitoring close to a term of 28 weeks to allow for fetal lung maturation. Surgical intervention can be performed when the estimated fetal mass is greater than 1000 grams or if the thickness of the myometrium at any point of the wall is less than 5 mm [<xref ref-type="bibr" rid="scirp.77989-ref5">5</xref>] .</p><p>Fewer than 5% of cases are recognized before laparotomy must be performed for hemorrhagic shock [<xref ref-type="bibr" rid="scirp.77989-ref11">11</xref>] . These pregnancies are also at risk of placenta accreta and percreta, probably because of the poor quality of the endometrium and low decidualization [<xref ref-type="bibr" rid="scirp.77989-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.77989-ref12">12</xref>] . In a series of 7 pregnancies implanted in the uterine rudimentary horn, Heinonen [<xref ref-type="bibr" rid="scirp.77989-ref13">13</xref>] noticed three cases of placenta accreta (43%), which was also favored by pathological examination of our case. In settings with limited access to health care resources, this condition could lead to maternal death.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Early diagnosis of a rudimentary horn pregnancy is usually accidental. Ultrasound examination may be a useful tool to detect these pregnancies in the first trimester. Abdominal pain occurring in the second trimester of pregnancy without identified cause should alert the clinician to this condition, and ultrasound examination will diagnose an intraperitoneal hemorrhage. Undiagnosed, this condition evolves towards uterine rupture and requires emergency surgery with excision of the rudimentary horn.</p></sec><sec id="s5"><title>Informed Consent</title><p>The patient had given her consent for the reported case to be published.</p></sec><sec id="s6"><title>Cite this paper</title><p>Didier, K.A., Roland, A.C., Joachim, K., D&#233;nis, E.N., KakouChales, Alice, D.F., Victor, K.S. and Firmin, K. (2017) Rupture of a Rudimentary Uterine Horn: A Case Report. Open Journal of Obstetrics and Gynecology, 7, 748-752. https://doi.org/10.4236/ojog.2017.77076</p></sec></body><back><ref-list><title>References</title><ref id="scirp.77989-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Nahum, G. (1998) Uterine Anomalies. How Common Are They, And What Is Their Distribution among Subtypes? The Journal of Reproductive Medicine, 43, 877-887.</mixed-citation></ref><ref id="scirp.77989-ref2"><label>2</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Johansen</surname><given-names> K. </given-names></name>,<etal>et al</etal>. 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