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      Cervicovaginal agenesis treated with modified Yang-Monti technique in two steps: Case report and literature review

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          Highlights

          • Müllerian duct anomalies are a rare entity.

          • We present the first case of cervicovaginal agenesis managed by the modified Yang-Monti technique in México.

          • We propose a modification of this technique by doing it in two steps.

          Abstract

          Introduction

          Müllerian duct anomalies are rare with less than 200 cases published in the literature. Recently, the implementation of the Yang-Monti principle for the creation of the neovagina has been used in 10 previous published cases. Here, we report the first case of cervicovaginal agenesis treated with the modified Yang-Monti technique in two steps in México.

          Presentation of case

          A 14-year-old female presented to the pediatric consult with a history of primary amenorrhea and a chronic-cyclic pelvic pain. She had normal external genitalia and secondary sexual characteristics, with a small vaginal pouch. Pelvic ultrasonography and magnetic resonance showed the absence of cervix and proximal vagina. The surgical approach was carried out in two steps. In the first, a neovagina was created with the modified Yang-Monti technique. On a second step one year after, the neovaginal dome was anastomosed with the uterus in a diamond shape, using Gore-tex ® in the cervicovaginal anastomosis, and a Foley catheter to prevent stenosis. After an 18-month follow-up, no complications have been observed. She has been taking Drospirenone and Ethinyl Estradiol with regular menstrual cycles.

          Discussion

          The surgical treatment of cervicovaginal agenesis has evolved. The advantages of the modified Yang-Monti technique lie in the possible diminution of the tension on the vascular pedicle, and the gained length of the neovagina. To perform this procedure in two steps, likely diminishes the risk of neovaginal ischemia and leakage of the anastomosis.

          Conclusion

          The two-steps modified Yang-Monti technique represents a safe alternative for the management of cervicovaginal agenesis.

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          Most cited references14

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          Mullerian duct anomalies: from diagnosis to intervention.

          The purpose of this study was to review the embryology, classification, imaging features and treatment options of Müllerian duct anomalies. The three embryological phases will be described and the appearance of the seven classes of Müllerian duct anomalies will be illustrated using hysterosalpingography, ultrasound and MRI. This exhibit will also review the treatment options, including interventional therapy. The role of imaging is to help detect, classify and guide surgical management. At this time, MRI is the modality of choice because of its high accuracy in detecting and accurately characterising Müllerian duct anomalies. In conclusion, radiologists should be familiar with the imaging features of the seven classes of Müllerian duct anomalies, as the appropriate course of treatment relies upon the correct diagnosis and categorisation of each anomaly.
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            • Abstract: found
            • Article: not found

            The presentation and management of complex female genital malformations.

            Common uterine anomalies are important owing to their impact on fertility, and complex mesonephric anomalies and certain Müllerian malformations are particularly important because they cause serious clinical symptoms and affect woman's quality of life, in addition to creating fertility problems. In these cases of complex female genital tract malformations, a correct diagnosis is essential to avoid inappropriate and/or unnecessary surgery. Therefore, acquiring and applying the appropriate embryological knowledge, management and therapy is a challenge for gynaecologists. Here, we considered complex malformations to be obstructive anomalies and/or those associated with cloacal and urogenital sinus anomalies, urinary and/or extragenital anomalies, or other clinical implications or symptoms creating a difficult differential diagnosis.
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              • Article: not found

              Congenital cervical atresia: report of seven cases and review of the literature.

              Our aim was to evaluate the clinical course and management of congenital cervical atresia. This retrospective analysis included 7 patients referred to our clinic and a review of the medical literature. Including this case series, 58 cases of congenital cervical atresia have been reported in the literature. Forty-eight percent of patients had isolated congenital cervical atresia with a normal vagina whereas the remainder had either complete or partial vaginal atresia ("shortened blind vaginal pouches"). Surgical management has included abdominal hysterectomy or uterovaginal cannulation with or without vaginoplasty. In 59% of patients who underwent uterovaginal canalization procedures (23/39), normal menstrual bleeding was achieved. Four of these patients subsequently became pregnant and were delivered at term. Surgical canalization in selected patients with congenital cervical atresia can be successfully performed to provide patients an opportunity for conservative management, resulting in normal menstrual bleeding, resolution of cyclic pelvic pain, and some potential (albeit limited) for fertility.
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                Author and article information

                Contributors
                Journal
                Int J Surg Case Rep
                Int J Surg Case Rep
                International Journal of Surgery Case Reports
                Elsevier
                2210-2612
                19 January 2017
                2017
                19 January 2017
                : 31
                : 176-179
                Affiliations
                [a ]Department of Pediatric Urology, Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Mexico
                [b ]Department of Gynecology and Obstetrics, Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Mexico
                [c ]Department of Genetics, Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Mexico
                [d ]Department of Radiology, Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Mexico
                [e ]Department of General Surgery, Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Mexico
                Author notes
                [* ]Corresponding author. plonecef@ 123456gmail.com
                [** ]Corresponding author at: Department of Pediatric Urology at the Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Salvador Quevedo y Zubieta street #750, Guadalajara, Jalisco, México.Department of Pediatric UrologyHospital Civil de Guadalajara “Dr. Juan I. Menchaca”Mexico jacostaleo@ 123456yahoo.com
                Article
                S2210-2612(17)30035-4
                10.1016/j.ijscr.2017.01.032
                5288454
                28157642
                35911dbf-0ef3-4012-9d28-6655a59f9f94
                © 2017 The Author(s)

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 4 October 2016
                : 12 January 2017
                : 14 January 2017
                Categories
                Case Report

                yang-monti technique,müllerian duct anomalies,cervicovaginal agenesis

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