==== Front J Turk Ger Gynecol Assoc J Turk Ger Gynecol Assoc JTGGA Journal of the Turkish German Gynecological Association 1309-0399 1309-0380 Galenos Publishing 31450882 10.4274/jtgga.galenos.2019.2019.0046 30075 Video Article Herlyn-Werner-Wunderlich Syndrome; laparoscopic treatment of obstructing longitudinal vaginal septum in patients with hematocolpos - a different technique for virgin patients Boyraz Gökhan 1*https://orcid.org/0000-0001-6165-1497 Karalok Alper 1https://orcid.org/0000-0002-0059-8773 Turan Taner 1https://orcid.org/0000-0001-8120-1143 Özgül Nejat 1 1 Clinic of Obstetrics and Gynecology, University of Health Sciences Turkey, Ankara Etlik Zübeyde Hanım Women’s Health Training and Research Hospital, Ankara, Turkey * Address for Correspondence: E-mail:gokhan.boyraz@gmail.com 12 2020 4 12 2020 21 4 303 304 6 3 2019 18 8 2019 © Copyright 2020 by the Turkish-German Gynecological Education and Research Foundation2020Journal of the Turkish-German Gynecological Association published by Galenos Publishing House.We aimed to define a new laparoscopic treatment approach for patients with hematocolpos and obstructed hemi-vagina due to longitudinal obstructing vaginal septum. This technique is particularly useful for patients who desire to preserve virginity. To the best of our knowledge this is the first case reporting laparoscopic resection of vaginal septum with an obstructed hemivagina and hematocolpos. Hematocolposlongitudinal vaginal septumHerlyn-Werner-Wunderlich Syndrome ==== Body Introduction Herlyn-Werner-Wunderlich Syndrome is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis and was initially described by Herlyn and Werner in 1971. The true incidence of this anomaly is unknown, however it has been reported between 0.1% and 3.8% (1,2). A 30-year-old patient presented with severe abdominal-pelvic pain and dysmenorrhea. Pelvic magnetic resonance imaging indicated a complete uterine septum coexisting with longitudinal obstructing vaginal septum that might cause hematocolpos. Unilateral renal agenesis was detected in computerized tomography urogram. She had not been sexually active and in spite of the severe pelvic pain she absolutely rejected vaginal surgery in order to preserve her hymeneal integrity and virginity. This situation forced the use of a laparoscopic approach. Therefore, we aimed to define a new laparoscopic treatment approach for the patients with hematocolpos and obstructed hemi-vagina due to longitudinal obstructing vaginal septum. This technique is particularly useful for patients who desire to preserve virginity. All of the techniques described previously were based on a vaginal approach and, to the best of our knowledge, this is the first case reporting laparoscopic resection of vaginal septum with an obstructed hemivagina and hematocolpos. This laparoscopic approach in patients with obstructing longitudinal vaginal septum with hematocolpos not only preserves hymeneal integrity but also enables definition of genital tract anomalies and coexisting anomalies exactly. The procedure consisted of two major steps (Video 1). Firstly, a transverse incision is made in the anterior vagina wall (Figure 1). Secondly, the longitudinal vaginal septum is resected (Figure 2) and transverse vaginal incision is closed with intra-corporeal suturing (Figure 3). Conclusion This first description of a laparoscopic approach seems to be an alternative treatment options in patients with hematocolpos, especially in those who desire to preserve virginity. Video 1. https://www.doi.org/10.4274/jtgga.galenos.2019.2019.0046.video1 Conflict of Interest: The authors declare no conflict of interest. Financial Disclosure: The authors declared that this study received no financial support. Figure 1 A wide hematocolpos corresponding to the obstructed left hemivagina Figure 2 Draining the old menstrual blood Figure 3 Fimbrial phimosis of left fallopian tube ==== Refs References 1 Zhu L Chen N Tong JL Wang W Zhang L Lang JH New classification of Herlyn-Werner-Wunderlich syndrome Chin Med J 2015 128 222 5 25591566 2 Herlyn U Werner H Simultaneous occurrence of an open Gartnerduct cyst, a homolateral aplasia of the kidney and a double uterus as a typical syndrome of abnormalities Geburtshilfe Frauenheilkd, 1971 31 340 7 5573697