Laparoscopic Management of Congenital Cervico-Vaginal Agenesis.

Nutan Jain, Reema Sircar
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Abstract

We report a case of cervical agenesis or lack of uterine cervix. It is a rare mullerian anomaly and occurs in 1 in 80,000-100,000 births. The patient presented to us with primary amenorrhea and cyclical left lower abdominal pain. She was diagnosed to have cervical agenesis associated with vaginal agenesis and left endometriotic cyst. Neovagina was created laparoscopically. Utero-vaginal anastomosis was tried but it was not technically feasible. Subsequently, laparoscopic hysterectomy was done due to recurrent endometriotic cyst formation.

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先天性宫颈阴道缺如的腹腔镜治疗。
我们报告了一例宫颈缺如或无宫颈的病例。这是一种罕见的穆勒氏畸形,每 8 万至 10 万新生儿中就有 1 例。患者因原发性闭经和周期性左下腹疼痛前来就诊。她被诊断为宫颈发育不全,伴有阴道发育不全和左侧子宫内膜异位囊肿。通过腹腔镜创建了新阴道。曾尝试子宫阴道吻合术,但技术上不可行。随后,由于复发性子宫内膜异位囊肿的形成,患者接受了腹腔镜子宫切除术。
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