A delayed therapy of dysmenorrhea due to noncommunicating rudimentary horn and unicornuate uterus: Case report and review of the literature
نویسندگان
چکیده
Although asymptomatic cases naturally occur, congenital mullerian abnormalities can present with infertility, menstrual irregularity and recurrent pregnancy loss. Women with normal reproductive outcomes and recurrent pregnancy loss exhibit approximately 2-4% and 5-10% incidence of various congenital mullerian abnormalities. Following septate uterus, bicornuate uterus and arcuate uterus, unicornuat uterus is the fourth most frequent congenital uterine abnormality seen in a combined population of infertile and fertile women. Unicornuate uterus with a non-communicating functional rudimentary horn is a type of mullerian anomaly and is a rare cause of dysmenorrhea. Here, we presented a case of this kind of abnormality and discussed the management strategies in the light of the literature.
منابع مشابه
Diagnostic and Laparoscopic Management of Unicornuate Uterus with Rudimentary Horn
We describe here a case report of a female patient with a unicornuate uterus with noncommunicating left rudimentary horn. The patient presented herself to us due to persistent lower abdominal pains, primarily dysmenorrhea and suspected internal genital endometriosis. Further to additional diagnosis and imaging by vaginal and abdominal ultrasound and abdominal MRI, a suspected rare congenital ma...
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Unicornuate uterus with a rudimentary horn is the rarest congenital anatomic anomaly of the female genital system, causing many obstetrical and gynecologic complications. The frequency of this pathology is approximately 1/100 000. A rudimentary horn usually develops following insufficient development of mullerian ducts. These patients present with dysmenorrhea, dyspareunia, and chronic pelvic p...
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INTRODUCTION A unicornuate uterus with a rudimentary horn is the most uncommon uterine anomaly of the female genital tract. It has an estimated frequency of one in 100,000 among the fertile female population. This anomaly results from the abnormal maturation of one Müllerian duct with the normal development of the contralateral one. CASE PRESENTATION We report here the case of a 14-year-old C...
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