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Online ISSN
1305-3124

Established
1993

Editors-in-Chief
​Cihat Şen, ​Nicola Volpe

Editors
Cecilia Villalain, Daniel Rolnik, M. Mar Gil

Managing Editors
Murat Yayla

Statistics Editor
Resul Arısoy

PP-06 Unicornuate uterus accompanied by unilateral tubal-agenesis in pregnancy a case presentation

Serem Kel, Nur Kuşcu, Süreyya Demir, Abdülbaki Şahan, Emine İrem Süha, Mehmet Nuri Duran, Bülent Demir

Article info

PP-06 Unicornuate uterus accompanied by unilateral tubal-agenesis in pregnancy a case presentation. Perinatal Journal 2023;31(2023):14 DOI: 10.59215/prn.23.031supp021

Author(s) Information

Serem Kel1,
Nur Kuşcu1,
Süreyya Demir2,
Abdülbaki Şahan1,
Emine İrem Süha1,
Mehmet Nuri Duran1,
Bülent Demir1

  1. Canakkale 18 Mart University Hospital, Çanakkale, Türkiye
  2. Canakkale Mehmet Akif Ersoy State Hospital, Çanakkale, Türkiye
Correspondence

Serem Kel, Canakkale 18 Mart University Hospital, Çanakkale, Türkiye,

Publication History

Earlyview Date: September 22, 2023

Publication date: October 01, 2023

Conflicts of Interest

No conflicts declared.

Objective

Fusion of the Müllerian ducts occurs during weeks 6-11 of pregnancy. Disruptions in this fusion process can lead to Müllerian duct anomalies. Among these anomalies, unicornuate uterus is the most common and is associated with pregnancy complications such as preterm labor. In this case presentation, we aim to present a patient with a diagnosis of unicornuate uterus and pelvic kidney, accompanied by unilateral tubal-ovarian absence, who gave birth at our clinic.

Case

A 26-year-old, G2P0A1 woman presented to the clinic at 33+4 weeks of gestation with high blood pressure. Upon reviewing the patient’s medical history, it was revealed that her first pregnancy ended in a miscarriage during the first trimester, and pelvic ultrasound detected an ectopic pelvic kidney. Further inquiry into the patient’s family history indicated that her mother also had an ectopic pelvic kidney. The patient was being followed up in our clinic with the threat of preterm delivery due to high blood pressure and contractions in the non-stress test .Considering the potential risk of preterm birth, the patient was administered two doses of betamethasone 24 hours apart for lung maturation. As high blood pressure and uterine contractions persisted during follow-up, a decision was made for delivery. The patient underwent a cesarean section. A live baby weighing 2180 grams with an 8-10 APGAR score and umbilical cord blood gas pH of 7.40 was delivered. Intraoperatively, a unicornuate appearance of the uterus without a rudimentary horn was observed, and the left fallopian tube and ovary were not seen. No complications arose during the operation. The patient was discharged on the third postoperative day.

Conclusion

Mullerian duct anomalies are observed in approximately 1-5% of the general population. The prevalence increases to around 13-25% in patients with a history of recurrent miscarriages. Unicornuate uterus is the most commonly encountered type among müllerian duct anomalies. The variation without a rudimentary horn accounts for approximately 35% of all unicornuate uteri. Kidney anomalies accompany approximately 40% of patients with unicornuate uterus. Patients with unicornuate uterus are often asymptomatic, and ultrasound alone might not be sufficient for diagnosis. Complications related to unicornuate uterus primarily manifest during pregnancy. Pregnant individuals with unicornuate uterus are at an increased risk of preterm birth, first and second-trimester miscarriages, intrauterine fetal death, and cesarean delivery. Pelvic kidney generally remains asymptomatic and is incidentally diagnosed. Its prevalence is approximately 1-10/10,000. In cases where a pelvic kidney is detected in female patients, the possibility of müllerian duct anomalies should be considered, and patients should be informed about potential pregnancy complications, especially in the context of such anomalies.
Keywords

Unicornuate uterus, pelvic kidney, preterm birth

  1. (Caserta, Mallozzi et al. 2014)
  2. (Reichman, Laufer, & Robinson, 2009)
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