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Laparoscopic Management of Cervical Agenesis: A Rare Case Report
Victoria L Crofts1, Dehlia Moussaoui2, Michal Yaron2
1Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals and University of Geneva, Geneva, Switzerland (All authors)..
This study details the successful laparoscopic treatment of a rare congenital obstructive Mullerian anomaly, specifically partial vaginal aplasia and cervical agenesis. The minimally invasive utero-vaginal anastomosis restored genital tract continuity, resolving pain and enabling regular menses.
Area of Science:
- Reproductive Medicine
- Minimally Invasive Surgery
- Pediatric Gynecology
Background:
- Congenital obstructive Mullerian anomalies are rare conditions affecting the female reproductive tract.
- Partial vaginal aplasia and cervical agenesis present unique diagnostic and management challenges.
- Cyclic pelvic pain in adolescents can be an indicator of underlying Mullerian anomalies.
Purpose of the Study:
- To describe the successful laparoscopic management of a rare case of partial vaginal aplasia and cervical agenesis.
- To illustrate the technique of direct laparoscopic utero-vaginal anastomosis for restoring genital tract continuity.
- To highlight the importance of a multidisciplinary approach in managing complex Mullerian anomalies.
Main Methods:
- A 13-year-old female with cyclic pelvic pain and suspected Mullerian anomaly underwent diagnostic imaging.
- Laparoscopic evaluation revealed partial vaginal aplasia, cervical agenesis, and a hematometra.
- A direct laparoscopic utero-vaginal anastomosis was performed to reconstruct the genital tract.
Main Results:
- The patient experienced immediate postoperative pain relief.
- Post-procedure vaginoscopy and hysteroscopy confirmed a patent utero-vaginal canal and uterus.
- At 2-year follow-up, the patient reported regular, painless menstrual cycles with no signs of stenosis.
Conclusions:
- Laparoscopic utero-vaginal anastomosis is an effective treatment for cervical agenesis with partial vaginal aplasia.
- Long-term follow-up is essential to monitor for complications and assess fertility potential.
- Multidisciplinary collaboration is crucial for optimal management of rare Mullerian anomalies.

