Boudhraa K, Barbarino A, Gara Mohamed Faouzi
Departement of Obstetrics and Gynecology, Mongi Slim Marsa Hospital, Tunis University, Tunis, Tunisia.
Tunis Med. 2008 Nov;86(11):1008-10.
Maldevelopment of the Müllerian duct system may result in various urogenital anomalies including didelphic uterus with a hypoplastic cervix and obstructed hemi-vagina.
We report a patient with this anomaly who was treated by laparoscopic hemi-hysterectomy and hysteroscopic resection of hemi-vagina. A 16-year-old patient who had complained of vaginal pus-like discharge on and off for 1 year was diagnosed by MRI to have a double uterus with obstructed right hemi-vagina and ipsilateral renal agenesis. After hysteroscopic identification of hypoplasia of the right uterine cervix, laparoscopic resection of the right uterus and right fallopian tube and hysteroscopic assisted resection of the vaginal septa were performed successfully.
We think that combined laparoscopy and hysteroscopy may be an effective alternative in the management and diagnosis of Mullerian anomalies.
苗勒管系统发育异常可能导致各种泌尿生殖系统畸形,包括双子宫伴宫颈发育不全和半阴道梗阻。
我们报告了一名患有这种畸形的患者,该患者接受了腹腔镜半子宫切除术和宫腔镜下半阴道切除术。一名16岁患者断断续续出现阴道脓性分泌物1年,经磁共振成像(MRI)诊断为双子宫,右侧半阴道梗阻且同侧肾缺如。在宫腔镜检查确定右侧子宫颈发育不全后,成功进行了腹腔镜下右侧子宫和右侧输卵管切除术以及宫腔镜辅助下阴道隔切除术。
我们认为腹腔镜和宫腔镜联合应用可能是诊断和处理苗勒管畸形的一种有效替代方法。