Abstract

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 malformation of the genital tract was established. A normal vagina with cervical system without pathological findings was presented during the operation. The diagnostic hysteroscopy and laparoscopy indicated an intact right unicornuate uterus with a regular tube and ovary. A left rudimentary horn, noncommunicating with cervix and vagina was also presented, also together with a regular tube and ovary. The chromopertubation carried out proved the patency of the right tube. The decision was taken intraoperatively to remove the left rudimentary horn with ipsilateral tube. The surgery could be carried out without complications. We are reporting a patient with persistent lower abdominal pain, who desires to have children, to conceive with a unicornuate uterus and left rudimentary horn with retrograde menstruation and proliferative endometrium. Surgical minimal invasive treatment by laparoscopically removing of the left rudimentary horn and tube took place.

Highlights

  • This paper reports on the case of a female patient with a unicornuate uterus and left rudimentary horn with retrograde menstruation and proliferative endometrium, who is willing to conceive

  • The left resectate consists of a rudimentary uterine horn with proliferative endometrium, regular tube with fimbriae without any suspected malignity

  • With concern to our case report, the decision to take out the rudimentary horn with ipsilateral tube was right

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Summary

Introduction

This paper reports on the case of a female patient with a unicornuate uterus and left rudimentary horn with retrograde menstruation and proliferative endometrium, who is willing to conceive. She suffers from a persistent lower abdominal pain. We removed the left rudimentary horn and tube using minimal invasive laparoscopy. We describe this case report, because it is a rare type of mullerian duct malformation and in our opinion, it has educational and scientific merits

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