摘要
<strong>Introduction:</strong><span style="font-family:;" "=""><span style="font-family:Verdana;"> Mullerian malformations are a group of malformations that result from an alteration of embryonic development. Most cases are asymptomatic, however, in pregnant </span><span style="font-family:Verdana;">patients</span><span style="font-family:Verdana;"> it has been associated with recurrent abortion or premature delivery. </span><b><span style="font-family:Verdana;">Case presentation:</span></b><span style="font-family:Verdana;"> 12 + 2 weeks pregnant woman consulted for abdominal pain, vomiting </span><span style="font-family:Verdana;">and</span><span style="font-family:Verdana;"> fever. During the study, a transvaginal ultrasound was performed, where two </span><span style="font-family:Verdana;">endometric</span><span style="font-family:Verdana;"> cavities and </span></span><span style="font-family:Verdana;">a </span><span style="font-family:Verdana;">pregnancy</span><span style="font-family:Verdana;"> in the right horn were observed. The evolution of the patient was torpid, reaching hypovolemic shock, resolved by an emergency laparotomy where the rupture of the right horn was found. </span><b><span style="font-family:Verdana;">Discu</span></b><b><span style="font-family:Verdana;">s</span></b><b><span style="font-family:Verdana;">sion</span></b><b><span style="font-family:Verdana;">: </span></b><span style="font-family:Verdana;">The bicornuate uterus is the consequence </span><span style="font-family:;" "=""><span style="font-family:Verdana;">of a partial fusion of the paramesonephric ducts </span><span><span style="font-family:Verdana;">during </span><span style="font-family:Verdana;">the fetal</span><span style="font-family:Verdana;"> development, resulting in two functional uterine horns. Pa</span></span><span style="font-family:Verdana;">tients with bicornuate uterus may be asymptomatic</span></span><span style="font-family:Verdana;">,</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> a
<strong>Introduction:</strong><span style="font-family:;" "=""><span style="font-family:Verdana;"> Mullerian malformations are a group of malformations that result from an alteration of embryonic development. Most cases are asymptomatic, however, in pregnant </span><span style="font-family:Verdana;">patients</span><span style="font-family:Verdana;"> it has been associated with recurrent abortion or premature delivery. </span><b><span style="font-family:Verdana;">Case presentation:</span></b><span style="font-family:Verdana;"> 12 + 2 weeks pregnant woman consulted for abdominal pain, vomiting </span><span style="font-family:Verdana;">and</span><span style="font-family:Verdana;"> fever. During the study, a transvaginal ultrasound was performed, where two </span><span style="font-family:Verdana;">endometric</span><span style="font-family:Verdana;"> cavities and </span></span><span style="font-family:Verdana;">a </span><span style="font-family:Verdana;">pregnancy</span><span style="font-family:Verdana;"> in the right horn were observed. The evolution of the patient was torpid, reaching hypovolemic shock, resolved by an emergency laparotomy where the rupture of the right horn was found. </span><b><span style="font-family:Verdana;">Discu</span></b><b><span style="font-family:Verdana;">s</span></b><b><span style="font-family:Verdana;">sion</span></b><b><span style="font-family:Verdana;">: </span></b><span style="font-family:Verdana;">The bicornuate uterus is the consequence </span><span style="font-family:;" "=""><span style="font-family:Verdana;">of a partial fusion of the paramesonephric ducts </span><span><span style="font-family:Verdana;">during </span><span style="font-family:Verdana;">the fetal</span><span style="font-family:Verdana;"> development, resulting in two functional uterine horns. Pa</span></span><span style="font-family:Verdana;">tients with bicornuate uterus may be asymptomatic</span></span><span style="font-family:Verdana;">,</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> a
