<?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">FMAR</journal-id><journal-title-group><journal-title>Forensic Medicine and Anatomy Research</journal-title></journal-title-group><issn pub-type="epub">2327-4115</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fmar.2017.54004</article-id><article-id pub-id-type="publisher-id">FMAR-80014</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>
 
 
  (Ventrodorsal) Symmetrical Bicornuate Uterus Mimicking a Pedunculated Myoma—A Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adam</surname><given-names>Moyosore Afodun</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>Khadijah</surname><given-names>Kofoworola Quadri</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mustapha</surname><given-names>Akajewole Masud</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Muhammad</surname><given-names>Olanrewaju Buhari</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sodiq</surname><given-names>Kolawole Lawal</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Physiology, College of Medicine, University of Lagos, Lagos, Nigeria</addr-line></aff><aff id="aff1"><addr-line>Department of Radiology, Ultrasound and Doppler Unit, Crystal Specialist Hospital, Lagos, Nigeria</addr-line></aff><aff id="aff3"><addr-line>Department of Anatomy, State University of Zanzibar, Zanzibar, Tanzania</addr-line></aff><aff id="aff4"><addr-line>Department of Anatomy, Faculty of Biomedical Science, Kampala International University, Kampala, Uganda</addr-line></aff><pub-date pub-type="epub"><day>31</day><month>10</month><year>2017</year></pub-date><volume>05</volume><issue>04</issue><fpage>33</fpage><lpage>38</lpage><history><date date-type="received"><day>3,</day>	<month>October</month>	<year>2017</year></date><date date-type="rev-recd"><day>28,</day>	<month>October</month>	<year>2017</year>	</date><date date-type="accepted"><day>31,</day>	<month>October</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>
 
 
  Uterine anomalies account for about 4% in the most sampled population. Here we report a case of a 35 years old woman with occasional complaint of suprapelvic “heaviness”. She had an abnormal menstrual circle for the last 6 years. Manual palpitations were unrevealing and she appeared externally healthy. HSG was earlier performed as part of a fertility intervention (wrongly concluding on a detached form of pedunculated-myoma). Ultrasound revealed 2 separated fundal-cones, uterine cavities and a single inferior cervix. Cyesis in the bicornuate uterus is usually high-risk, making patients with uterine anomalies prone to proven misdiagnosis (e.g. appendicitis) and infertility. In addition, sonar further showed bilateral ovarian torsion. Corrective surgery was done in a hospital; post surgical healing was normal and uneventful.
 
</p></abstract><kwd-group><kwd>Bicornuate</kwd><kwd> Ultrasound</kwd><kwd> Fertility</kwd><kwd> Population</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The Latin word “cornu” means horn. A bicornuate uterus, a fused type of uterine malformation in humans is “normal” amongst other mammals like rats, mice and pigs. Tubal Mullerian anomaly accounts for bicornuate 39%, arcuate 7%, septated-uterus 34%, aplastic &gt; 5% and other uterine structural defects [<xref ref-type="bibr" rid="scirp.80014-ref1">1</xref>] . Bicornuate uterus being a disorder of Mullerian ducts [<xref ref-type="bibr" rid="scirp.80014-ref2">2</xref>] is distinct from type II uterine didelphys which sometimes have two vaginas/external genitalia.</p><p>There are reported cases of IVF failure in a bicornuate uterus and some increased incidence of ectopic pregnancy complications [<xref ref-type="bibr" rid="scirp.80014-ref3">3</xref>] . Kumar et al. (2008) [<xref ref-type="bibr" rid="scirp.80014-ref4">4</xref>] in a study reported that MRI showing bicornuate uterus exposed cervical agenesis. Some studies [<xref ref-type="bibr" rid="scirp.80014-ref5">5</xref>] have cited septate uterus as the 2<sup>nd</sup> most common uterine anomaly after bicornuate uterus [<xref ref-type="bibr" rid="scirp.80014-ref6">6</xref>] . Surgically treated didelphic uterus according to Heinonen (2000) [<xref ref-type="bibr" rid="scirp.80014-ref7">7</xref>] has encouraging fertility prognosis when compared to a bicornuate uterus. Pregnancy rarely occurs in the horn of a unicornuate uterus [<xref ref-type="bibr" rid="scirp.80014-ref8">8</xref>] .</p><p>A longitudinal study [<xref ref-type="bibr" rid="scirp.80014-ref9">9</xref>] observed that antenatal women with monitored (ultrasound) history were at lower risk of having uterine anomalies. Accurate statistical percentage and incidence of Mullerian abnormality in a population is difficult to estimate due to its rarity [<xref ref-type="bibr" rid="scirp.80014-ref10">10</xref>] . Malfusion of the mesonephric duct (M&#252;llerian) in utero results in different uterine anomalies [<xref ref-type="bibr" rid="scirp.80014-ref11">11</xref>] . Data linking Caesarian sections, PROM (premature rupture of membrane), breach-lie/presentations to uterine anomalies are mostly from case reports, structural anatomic variations or micro-studies [<xref ref-type="bibr" rid="scirp.80014-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.80014-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.80014-ref14">14</xref>] . Advances in 3D and 4D (i.e., 3D in real-time) ultrasound have led to non-invasive observations of these anomalies [<xref ref-type="bibr" rid="scirp.80014-ref9">9</xref>] .</p></sec><sec id="s2"><title>2. Case Report</title><p>A middle-aged woman suspected to be from a high-socio-economic background reported at the Radiological Department of Crystal Specialist Hospital (CSH), Dopemu-Akowonjo, Lagos, Nigeria. Ultrasound was performed with a Logic 3―Pro General Electric (GE) ultrasound machine (made in USA); 3.5 MH<sub>z</sub> curvilinear transducer. She had a turbulent menstrual cycle, with fluctuating amenorrhea and sometimes/occasional episodes of excessive bleeding. “Frozen” sonograms confirmed bicornuate uterus; though the (bilateral) ovaries were distal in position, they appeared normal in collaboration with structural anatomical plane.</p><p>Oral-patient interaction yielded no significant family history of rhesus-factor incompatibility, or consanguineous marriage by relatives. According to medical-records, the patient was nulliparous, weighed 61 kg and had copious “whitish” discharge noted by the attending physician during speculum examination of the cervix and external os. Informed consent was sought from patient and granted by Crystal Specialist Hospital for documentation of this case in line with the 1975 Helsinki Declaration on patient-rights and confidentiality.</p><p>Surgical treatment of the patient was not done or carried out in our hospital (CSH); however, information reached us that her postoperative recovery was uneventful with skin stitches removed after 8 days. Follow-up data also revealed dressing was done on the 2<sup>nd</sup> postoperative day and patient discharged on the 9<sup>th</sup> day.</p></sec><sec id="s3"><title>3. Discussion</title><p>Diagnosis of a bicornuate uterus in other to differentiate it with split-uterine-didelphys can be by hysteroscopy, ultrasound, HSG and laparoscopy. It should be noted that in a septated uterus, a thick persistent longitudinal septum partially separates the uterine cavity superiorly as opposed to a bicornuate variation (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Our ultrasound findings are in agreement with a retrospective study [<xref ref-type="bibr" rid="scirp.80014-ref10">10</xref>] on didelphys uterus and bicornuate uteri; they (researchers) noted patients with the anomalies required sustained infertility treatments. Parallel to Jayasinghe et al. (2005) [<xref ref-type="bibr" rid="scirp.80014-ref15">15</xref>] and majority of obstetricians, if a confirmed diagnosis of cyesis occurs in the rudimentary horn (see <xref ref-type="fig" rid="fig2">Figure 2</xref>, u2), immediate surgery must be performed. Since there is a failure in the complete development of both Mullerian ducts with incomplete fusion, the fused lower portion forms the main cervical and uterovaginal area (<xref ref-type="fig" rid="fig2">Figure 2</xref>, u1).</p><p>Severe dysmenorrhea, occasional cervical duplication [<xref ref-type="bibr" rid="scirp.80014-ref16">16</xref>] make gravidae a daunting task in women with the bicornuate uterus; being mostly in “compressed” form of birth defects. A plausible explanation for irregular uterine anomalies is decreased muscle mass and blood flow in uterine arteries. Incidence of this rare anomaly varies and may affect gynecological structure and obstetric outcome [<xref ref-type="bibr" rid="scirp.80014-ref2">2</xref>] . Greater than 60% of women with malformed uterus may stay completely asymptomatic. Cephalic part of the bicornuate uterus appears bifurcated (<xref ref-type="fig" rid="fig1">Figure 1</xref>) while the caudal part is normal. The symmetry of uterine cavities in bicornuate uterus creates certain fissional communication inferiorly. In the branched horn (<xref ref-type="fig" rid="fig1">Figure 1</xref>) if the angle of one uterine cavity is equal or less than 75 degrees, a septate uterus is formed [<xref ref-type="bibr" rid="scirp.80014-ref17">17</xref>] . Likely haematometra and cryptomenorrhea is a chronology likely to develop in the rudimentary horn (<xref ref-type="fig" rid="fig2">Figure 2</xref>, u2).</p><p>In agreement with Reuter et al., (1989) [<xref ref-type="bibr" rid="scirp.80014-ref17">17</xref>] sonography will rule-out pressure of pedunculated/fistulic or septated uterine component; since it is at a wide angle 75˚ - 102˚. In contrast to our case report, unicornuate uterus indicates “single-horned” with a RT or LT adnexae, with a small AP diameter parallel to the cervix; while a didelphic variant exhibits 2 (cervical and endometrial) canals [<xref ref-type="bibr" rid="scirp.80014-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.80014-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.80014-ref20">20</xref>] . Paired mesonephric ducts are incompletely fused in a “dented” fundus. Bicornuate uterus can also be caused by resorption defects, malrotation fusions during embryonic stage, with an angle separating the 2 horns not greater than (&gt;) 105˚ [<xref ref-type="bibr" rid="scirp.80014-ref18">18</xref>] ; as opposed to a normal uterus (control) seen in <xref ref-type="fig" rid="fig3">Figure 3</xref>, marked probe tenderness was present in the right fornix. Normal uteri women have better reproductive outcome and higher pregnancy rate compared with those with anomalies. Without a doubt, they belong to a high- risk group and it is of great importance for sonologists to detect reproductive tract anatomic variations by ultrasound early. The widely divergent apices and bi-fundus of the bicornuate uterus makes hysteroplastic unity a theoretical possibility.</p></sec><sec id="s4"><title>4. Conclusions</title><p>Conception and fertility in bicornuate uteri remains a controversial topic among radiologists and gynecologists. Elusive data on surgical correction: (partial) hysterectomy, metroplasty or myomectomy (as the case may apply) remains sparse.</p><p>Strassman’s utriculoplasty surgery could be helpful in correcting women with a bicornuate uterus. This procedure will allow for fusion of the bi-uterine cavity and fundus. Incision for uniting uterine cavity improves parturitional outcome in bicornuate patients who had earlier suffered abortions. Real-time ultrasound should be considered to exclude Herlyn-Werner-Wunderlich (HWW) syndrome.</p></sec><sec id="s5"><title>Cite this paper</title><p>Afodun, A.M., Quadri, K.K., Masud, M.A., Buhari, M.O. and Lawal, S.K. (2017) (Ventrodorsal) Symmetrical Bicornuate Uterus Mimicking a Pedunculated Myoma―A Case Report. Forensic Medicine and Anatomy Research, 5, 33-38. https://doi.org/10.4236/fmar.2017.54004</p></sec></body><back><ref-list><title>References</title><ref id="scirp.80014-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Cunningham, F.G., Leveno, K.J., Bloom, S.L., Hauth, J.C., Rose, D.J. and Spong, C.Y. (2010) Reproductive Tract Abnormalities. In: Cunningham, F.G., Ed., Williams Obstetrics, 23rd Edition, McGraw Hill, New York, 895-896.</mixed-citation></ref><ref id="scirp.80014-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Suwal, A. and Kumar, A. (2010) Complete Bicornuate Uterus with Complete Longitudinal Vaginal Septum. Journal of Nepal Medical Association, 49, 243-246.</mixed-citation></ref><ref id="scirp.80014-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Singh, N., Singh, U. and Verma, M.L. (2013) Ruptured Bicornuate Uterus Mimicking Ectopic Pregnancy: A Case Report. Journal of Obstetrics and Gynaecology Research, 39, 364-366. https://doi.org/10.1111/j.1447-0756.2012.01914.x</mixed-citation></ref><ref id="scirp.80014-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Kumar, S., Singh, S.K., Mavuduru, R., Naveen, A., Agarwal, M.M., Vanita, J., et al. (2008) Bicornuate Uterine Horns with Complete Cervical-Vaginal Agenesis and Congenital Vesico-Uterine Fistula. International Urogynecology Journal and Pelvic Floor Dysfunc-tion, 19, 739-741. https://doi.org/10.1007/s00192-007-0507-5</mixed-citation></ref><ref id="scirp.80014-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Nahum, G.G. (1998) Uterine Anomalies. How Common Are They, and What Is Their Distribution among Subtypes? Journal of Reproductive Medicine, 43, 877-887.</mixed-citation></ref><ref id="scirp.80014-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Speroff, L. and Fritz, M.A. (2005) Clinical Gynecologic Endocrinology and Infertility. 7th Edition, Lippincott Williams &amp; Wilvins, Philadelphia.</mixed-citation></ref><ref id="scirp.80014-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Heinonen, P.K. (2000) Clinical Implications of the Didelphic Uterus: Long Term Fol-low-Up of 49 Cases. European Journal of Obstetrics and Gynecology and Reproductive Biology, 91, 183-190. https://doi.org/10.1016/S0301-2115(99)00259-6</mixed-citation></ref><ref id="scirp.80014-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Tufail, A. and Hasmi, H.A. (2007) Ruptured Ectopic Pregnancy in a Rudimentary Horn of the Uterus. Journal of College of Physicians and Surgeons Pakistan, 17, 105-106.</mixed-citation></ref><ref id="scirp.80014-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Woelfer, B., Salim, R. and Jurkovic, D. (2001) Reproductive Outcomes in Women with Congenital Uterine Anomalies Detected by Three-Dimensional Ultrasound Screening. Obstetrics &amp; Gynecology, 98, 1099-1103.</mixed-citation></ref><ref id="scirp.80014-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, Y., Zhao, Y. and Qiao, J. (2010) Obstetric Outcome of Women with Uterine Anomalies in China. Chinese Medical Journal, 123, 418-422.</mixed-citation></ref><ref id="scirp.80014-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Ahmad, F.K., Sherman, S.J. and Hagglund, K.H. (2000) Twin Gestation in a Woman with a Uterus Didelphys. A Case Report. The Journal of Reproductive Medicine, 45, 357-359.</mixed-citation></ref><ref id="scirp.80014-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Reichman, D., Lauger, M.R. and Robinson, B.K. (2009) Pregnancy Outcomes in Unicor-nuate Uteri: A Review. Fertility and Sterility, 91, 1886-1894.</mixed-citation></ref><ref id="scirp.80014-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Akar, M.E., Bayer, D., Yildiz, S., et al. (2005) Reproductive Outcome of Women with Unicornuate Uterus. Australian and New Zealand Journal of Obstetrics and Gynaecology, 45, 148-150. https://doi.org/10.1111/j.1479-828X.2005.00346.x</mixed-citation></ref><ref id="scirp.80014-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Rackow, B.W. and Arici, A. (2007) Reproductive Performance of Women with Müllerian anomalies. Current Opinion in Obstetrics &amp; Gynecology, 19, 229-237.  
https://doi.org/10.1097/GCO.0b013e32814b0649</mixed-citation></ref><ref id="scirp.80014-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Jayasinghe, Y., Rane, A. and Staleuki, H. (2005) The Presentation and the Early Diagnosis of a Rudimentary Horn. Obstetrics &amp; Gynecology, 105, 1456-1467.  
https://doi.org/10.1097/01.AOG.0000161321.94364.56</mixed-citation></ref><ref id="scirp.80014-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Ribeiro, S.C., Yamakami, L.Y., Tormena, R.A., et al. (2010) Septate Uterus with Cervical Duplication and Longitudinal Vaginal Septum. Revista Da Associacao Medica Brasileira, 56, 254-256. https://doi.org/10.1590/S0104-42302010000200029</mixed-citation></ref><ref id="scirp.80014-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Reuter, K.L., Daly, D.C. and Cohen, S.M. (1989) Septate versus Bicornuate Uteri: Errors in Imaging Diagnosis. Radiology, 172, 749-752.  
https://doi.org/10.1148/radiology.172.3.2528160</mixed-citation></ref><ref id="scirp.80014-ref18"><label>18</label><mixed-citation publication-type="book" xlink:type="simple">Zwiebel, W.J. (1983) Pelvic Congenital Anomalies and Pubertal Disorders. In: Zwiebel, W.J., Ed., Introduction to Ultrasound, Saunders, Philadelphia, 294-296.</mixed-citation></ref><ref id="scirp.80014-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Troiano, R.N. and McCarthy, S.M. (2004) Müllerian Duct Anomalies: Imaging and Clinical Issues. Radiology, 233, 19-34.</mixed-citation></ref><ref id="scirp.80014-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Afodun, A.M., Ayinde, T.O., Quadri, K.K. and Masud, M.A. (2015) Concise Human Chorionic Atlas (Ultrasound, Gross, Histopathologic and Eponymical Approach). 1st Edition (Organ-Series), Xlibris Publishers, 50 p.  
https://www.xlibris.com/Bookstore/BookDetail.aspx?BookId=SKU-001001968</mixed-citation></ref></ref-list></back></article>