Poliquin Vanessa, Victory Rahi, Vilos George A
Schulich School of Medicine and Dentistry, University of Western Ontario, Canada.
J Minim Invasive Gynecol. 2008 Mar-Apr;15(2):152-60. doi: 10.1016/j.jmig.2007.12.009.
We report a case of retroperitoneal leiomyoma and a systematic review of the literature regarding this finding. A 45-year-old woman with menorrhagia and a complex pelvic mass underwent preoperative imaging and consequent total abdominal hysterectomy and bilateral salpingo-oophorectomy. Histopathology revealed a 13-cm retroperitoneal, pedunculated leiomyoma arising from the uterus anterior to the internal cervical os. Literature review identified 105 cases of retroperitoneal leiomyomata from 1941 through 2007, with 37 cases, including our own, containing sufficient information for analysis. Abstracted variables included patient age, race, obstetric and gynecologic history, presentation and duration of symptoms, investigations, management, surgical findings, pathologic and immunohistochemical characteristics, duration of follow-up, evidence of recurrence and its management. Mean age (+/-SD) of the population was 46.27 +/- 13.19 years. More than 40% of patients had either undergone hysterectomy for uterine leiomyomata previously or had concurrent uterine leiomyomata. Of patients, 25% were asymptomatic, 31.3% experienced abdominal fullness, 18.8% had urinary symptoms, 18.8% had weight loss, and 18.8% had pelvic pain. Diagnostic evaluation was inconclusive and surgical excision was undertaken in all but 1 case. Median leiomyoma size was 12.0 cm (range 2.0-37.0 cm) with most in the posterior retroperitoneum, independent of the uterus. Pathologic and immunohistochemical investigations were comparable with those of uterine leiomyomata. Surgery was mostly curative with 5 reported cases of recurrence, 3 of which were then considered sarcomatous. Retroperitoneal leiomyomata present diagnostic and therapeutic challenges, and as such require heightened surveillance.
我们报告一例腹膜后平滑肌瘤病例,并对有关该发现的文献进行系统综述。一名45岁月经过多且有复杂盆腔肿物的女性接受了术前影像学检查,随后进行了全腹子宫切除术及双侧输卵管卵巢切除术。组织病理学检查发现一个13厘米的腹膜后带蒂平滑肌瘤,起源于子宫颈内口前方的子宫。文献综述确定了1941年至2007年间105例腹膜后平滑肌瘤病例,其中37例(包括我们自己的病例)包含足够的分析信息。提取的变量包括患者年龄、种族、妇产科病史、症状表现及持续时间、检查、治疗、手术发现、病理和免疫组化特征、随访时间、复发证据及其处理。该人群的平均年龄(±标准差)为46.27±13.19岁。超过40%的患者既往曾因子宫平滑肌瘤接受过子宫切除术或同时患有子宫平滑肌瘤。患者中,25%无症状,31.3%有腹部胀满感,18.8%有泌尿系统症状,18.8%有体重减轻,18.8%有盆腔疼痛。诊断性评估结果不明确,除1例患者外其余均接受了手术切除。平滑肌瘤的中位大小为12.0厘米(范围2.0 - 37.0厘米),大多数位于后腹膜,与子宫无关。病理和免疫组化检查结果与子宫平滑肌瘤相似。手术大多可治愈,报告有5例复发,其中3例后来被认为是肉瘤。腹膜后平滑肌瘤带来诊断和治疗挑战因此需要加强监测。