Di Spiezio Sardo Attilio, Giampaolino Pierluigi, Scognamiglio Marianna, Varelli Carlo, Nazzaro Giovanni, Mansueto Gelsomina, Nappi Carmine, Grimbizis Grigoris F
Department of Obstetrics and Gynecology, University of Naples "Federico II", Naples, Italy.
Department of Obstetrics and Gynecology, University of Naples "Federico II", Naples, Italy.
J Minim Invasive Gynecol. 2016 Jan;23(1):16-7. doi: 10.1016/j.jmig.2015.09.006. Epub 2015 Sep 21.
To report the combined hysteroscopic and laparoscopic treatment of a complete septate uterus with unilateral cervical aplasia (class U2bC3V0/ESHRE/ESGE classification) and isolated mullerian remnants.
Step-by-step presentation of the surgical treatment (Canadian Task Force classification 4).
Complete septate uterus with unilateral cervical aplasia (formally Robert's uterus) is characterized by the presence of a uterine septum completely dividing the endometrial cavity into an obstructed hemicavity and a contralateral nonobstructing hemicavity connected normally to the existing cervix. It has always been described as isolated without any associated anomaly.
A 30-year-old woman was referred to our department for dysmenorrhea and primary infertility. Hysterosalpingography showed the presence of a right (RT) hemiuterus with a patent fallopian tube; further evaluation with 2- and 3-dimensional ultrasound and magnetic resonance imaging showed an externally normal-appearing uterus, a right normal hemicavity connected normally with the existed cervix and, a left hemicavity fully divided from the right one by a complete septum and not connected with the cervix. Interestingly, a peculiar complex mass with cystic areas, attached posterolaterally from the left side to the uterine wall at the level of the isthmus and the upper cervix, was also diagnosed.
The study protocol was approved by our local institutional review board. During outpatient hysteroscopy, a right uterine hemicavity with a single ostium was identified without any communication with the left hemicavity. The patient was then scheduled for combined laparoscopic and hysteroscopic treatment. During laparoscopy, a normal uterine body with multiple myomas and a pseudocystic lesion attached posteriorly and left laterally to the uterus at the level of the isthmus and the upper cervix were shown; no communication between the cystic part of that lesion and the isthmus or the cervicovaginal canal was observed. During hysteroscopy, a longitudinal incision of the septum with a 5F bipolar electrode was performed; the left hemicavity was opened, and the corresponding tubal ostium was identified. The pseudocystic lesion was then excised after opening and sent for pathological analysis; the defect was closed with interrupted intracorporeal knots.
A single normal endometrial cavity with both tubal ostia was obtained, thus restoring obstruction by unification of the uterine cavity. A histologic report of the removed pseudocystic lesion was compatible with the diagnosis of mullerian remnants. A follow-up hysteroscopy 3 months after showed a normal uterine cavity without postsurgical adhesions.
The use of 3-dimensional ultrasound and magnetic resonance imaging in combination with the new ESHRE/ESGE classification system gives the opportunity to obtain a precise representation of the female genital anatomy even in the presence of complex anomalies. Although a septate uterus with unilateral cervical aplasia has been already described, the presence of mullerian remnants is a rare entity associated with cyclic pelvic pain, thus needing adequate recognition and treatment. The combined hysteroscopic and laparoscopic approach offers a unique opportunity for the treatment of complex anomalies.
报告宫腔镜与腹腔镜联合治疗完全纵隔子宫合并单侧宫颈发育不全(U2bC3V0/ESHRE/ESGE分类)及孤立性苗勒管残件的情况。
手术治疗的分步介绍(加拿大工作组分类4级)。
完全纵隔子宫合并单侧宫颈发育不全(原称罗伯特子宫)的特征是存在一个子宫纵隔,将子宫内膜腔完全分为一个梗阻性半腔和一个对侧通畅的半腔,该通畅半腔与现存宫颈正常相连。一直以来,其被描述为孤立存在,无任何相关异常。
一名30岁女性因痛经和原发性不孕转诊至我科。子宫输卵管造影显示右侧半子宫及输卵管通畅;二维和三维超声及磁共振成像进一步评估显示子宫外观正常,右侧半腔正常且与现存宫颈正常相连,左侧半腔被完整纵隔与右侧完全分隔且未与宫颈相连。有趣的是,还诊断出一个特殊的复杂肿物,有囊性区域,从左侧附着于子宫峡部和宫颈上段的后壁。
本研究方案经当地机构审查委员会批准。门诊宫腔镜检查时,发现右侧子宫半腔有单个开口,与左侧半腔无连通。随后患者安排进行腹腔镜与宫腔镜联合治疗。腹腔镜检查时,显示子宫体正常,有多个肌瘤,子宫峡部和宫颈上段后壁及左侧有一个假性囊性病变;未观察到该病变的囊性部分与峡部或宫颈阴道管之间有连通。宫腔镜检查时,用5F双极电极对纵隔进行纵向切开;打开左侧半腔,确定相应的输卵管开口。然后在打开后切除假性囊性病变并送病理分析;缺损用体内间断缝合关闭。
获得了一个有双侧输卵管开口的单一正常子宫内膜腔,通过子宫腔的联合恢复了梗阻。切除的假性囊性病变的组织学报告与苗勒管残件的诊断相符。术后3个月的随访宫腔镜检查显示子宫腔正常,无术后粘连。
三维超声和磁共振成像与新的ESHRE/ESGE分类系统联合使用,即使在存在复杂异常的情况下,也能准确呈现女性生殖器官的解剖结构。虽然完全纵隔子宫合并单侧宫颈发育不全已被描述过,但苗勒管残件的存在是一种与周期性盆腔疼痛相关的罕见情况,因此需要充分认识和治疗。宫腔镜与腹腔镜联合方法为治疗复杂异常提供了独特的机会。