Abstract

Background: The Vagina is a composite structure formed partly from the mullerian duct and partly from urogential sinus. Most of the patients with mullerian agenesis have small rudimentary uterus without any endometrial cavity, 7% - 8% may have functioning uterus. Case: A 15 years old girl admitted with primary amenorrhea, cyclical abdominal pain, hematometra and complete vaginal agenesis. Surgical correction is the mainstay of treatment in patients with functioning uterus and absent vagina. Vaginoplasty was done to reconstruct a neovagina using amnion graft and establish uterovaginal continuity. In this case we have used only perineal approach to dissect the neovagina and identify the cervix with formation of a patent drainage tract and adequate vaginal length of 9 cm. Conclusion: In rare cases of obstructed functioning uterus by complete vaginal agenesis, vaginoplasty effectively restores anatomy and function by an overall minimal operative morbidity. Human amnion provides excellent results in neovaginal reconstruction.

Highlights

  • Vaginal agenesis is a congenital anomaly of the female genital tract and may occur as isolated developmental defect or as part of a complex of anomalies

  • Normal secondary sexual characteristics presented with primary amenorrhea and cyclic pelvic pain for six months on examination her vitals were stable with pulse 84 per minute and BP 120/84 mm of Hg

  • We here report a similar case of hematometra with complete vaginal agenesis

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Summary

INTRODUCTION

Vaginal agenesis is a congenital anomaly of the female genital tract and may occur as isolated developmental defect or as part of a complex of anomalies. Vaginal agenesis is estimated to occur in 1 in 4000 - 5000 live female births [1]. It is most commonly associated with MayorRokitansky-Kuster-Hauser (MRKH) syndro-me and androgen insensitivity syndrome [2,3]. Isolated defects in the development of vagina though very rare but have been reported in literature [4]. We here report a similar case of hematometra with complete vaginal agenesis

CASE REPORT
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