Abstract

Cervicovaginal atresia with a functional uterus is rare. There are no established surgical methods to treat this condition, and only a few reports have been published on surgical techniques. Furthermore, postoperative complications, such as restenosis, often require reoperation. A 19-year-old woman was pointed out cervical hypoplasia and referred to our hospital for further examination and treatment. A pelvic examination revealed that the vagina had a slight recession with a blind end. Transrectal ultrasound and pelvic magnetic resonance imaging revealed congenital vaginal agenesis and cervical hypoplasia. Elective surgery was performed after reshaping the vagina. A radical surgery was performed 10 months later after sufficient self-dilation by using Frank's technique in an outpatient setting. At first, we approached by laparoscopically to correct autologous peritoneum and to bladder detach, then the cervical canal was identified. Next, a skin biopsy punch was used several times to hollow out the cervical tissue to shape and expand the cervical canal. A catheter was then placed in the uterus and autologous peritoneum was wrapped around it and fixed to the cervical canal. The catheter was removed 6 weeks postoperatively, and the patient continued dilating her vagina until she was able to have sexual intercourse, and then stopped the self-dilation. Eight months postoperatively, the patient did not report any menstrual irregularities. It is important to make corrections to prevent restenosis of the vagina and cervical canal and prevent the symptoms from recurring. Make use of autologous peritoneum as graft onto the cervical canal is effective method for the treatment of cervicovaginal atresia.

Highlights

  • Case PresentationThe patient was a 19-year-old nulligravida woman who was examined for primary amenorrhea at another hospital

  • Communication between the shaped cervical canal and the dilated uterine cavity was created. (e) Vaginal approach An H/S Elliptosphere catheter (CooperSurgical, CT, USA) used for hysterosalpingography was placed in the uterine cavity (►Fig. 5). (f) Vaginal approach The laparoscopically harvested autologous peritoneum was wrapped around the catheter and fixed in the cervical canal

  • Cervicovaginal atresia is even rarer, with less than 200 cases reported from when it was first described by Roberts et al from 1942 to 2011.1 Only 2 to 7% of cervicovaginal atresia cases have functional uteruses with vaginal agenesis.[2]

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Summary

Case Presentation

The patient was a 19-year-old nulligravida woman who was examined for primary amenorrhea at another hospital. The vulva was normal, but vaginal agenesis was observed; the uterine cervix was restiform shaped, and the received June 9, 2019 accepted after revision October 28, 2019. Novel Method of Cervicoplasty Fujino et al 29 cervical canal line structure was indistinct, which indicated cervical hypoplasia. The patient was referred to our hospital for further examination and treatment. A pelvic examination revealed that the vagina had a slight recession with a blind end. Transrectal ultrasonography showed absence of a cervical canal line in the uterine cervix, fluid accumulation in the intrauterine cavity, and normal ovaries on both sides. Congenital vaginal agenesis and cervical hypoplasia were diagnosed and a decision was made to perform an elective surgery

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