Jain Nutan, Sircar Reema
Vardhman Infertility and Endoscopy Centre, Muzaffarnagar, Uttar Pradesh, India.
Department of Obstetrics and Gynecology, CMC and H, Ludhiana, Punjab, India.
J Gynecol Endosc Surg. 2011 Jul-Dec;2(2):94-6. doi: 10.4103/0974-1216.114158.
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.
我们报告一例宫颈发育不全或宫颈缺如的病例。这是一种罕见的苗勒管异常，在80000 - 100000例出生中出现1例。该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合并阴道发育不全及左侧子宫内膜异位囊肿。通过腹腔镜创建了新阴道。尝试进行子宫 - 阴道吻合术，但在技术上不可行。随后，由于复发性子宫内膜异位囊肿形成，进行了腹腔镜子宫切除术。
