Atlanta Center for Minimally Invasive Surgery and Reproductive Medicine, Atlanta, GA.
Northwell Health Hospital-Gynecology, Queens County, New York, NY.
CRSLS. 2022 Jan 25;9(1). doi: 10.4293/CRSLS.2021.00080. eCollection 2022 Jan-Mar.
Endometriosis spreading to the vagina is rare, present in only 0.02% of women with symptomatic endometriosis. Suburethral lesion site is exceptional. In an extensive literature review only 4 cases of suburethral endometriosis were identified. Our objective is to present a case of primary vaginal suburethral endometriosis in a 31-year old patient who underwent laparoscopic evaluation and to perform a literature review on this topic.
Case report presentation based on information extracted from patient database. A review of literature with a Medline search using key words urethral endometriosis, suburethral endometriosis, or urethral diverticulum was undertaken.
This case report describes a case of a 31-year old female patient referred for severe pelvic pain, worsening during menstruation. On physical examination a 2 cm suburethral endometriotic lesion was found as the initial presentation. Her examination was also significant for enlarged, tender uterus and adnexa. Based on examination and imaging, adenomyosis and endometriosis were suspected. Surgical evaluation revealed extensive endometriosis with lymph node involvement at laparoscopic exploration. The review of literature revealed only 4 cases where suburethral endometriosis was previously identified.
Primary vaginal suburethral endometriosis, although rare, could be an indication of extensive endometriosis. This case highlights the importance of careful clinical examination, surgical excision, and laparoscopic evaluation when identifying suburethral vaginal endometriotic lesions.
子宫内膜异位症转移到阴道非常罕见,仅见于 0.02%有症状的子宫内膜异位症女性。尿道下病变部位非常罕见。在广泛的文献回顾中,仅发现了 4 例尿道下子宫内膜异位症。我们的目的是报告一例 31 岁患者的原发性阴道尿道下子宫内膜异位症,并对该主题进行文献回顾。
基于从患者数据库中提取的信息,进行病例报告介绍。通过使用关键词尿道子宫内膜异位症、尿道下子宫内膜异位症或尿道憩室进行 Medline 搜索,对文献进行回顾。
本病例报告描述了一名 31 岁女性患者因严重盆腔疼痛就诊,月经期间疼痛加剧。体格检查发现 2cm 尿道下子宫内膜异位症病变。她的检查还显示子宫和附件增大、触痛。根据检查和影像学检查,怀疑为腺肌病和子宫内膜异位症。手术评估显示腹腔镜探查时广泛的子宫内膜异位症伴淋巴结受累。文献回顾仅发现了 4 例先前确定的尿道下子宫内膜异位症病例。
虽然原发性阴道尿道下子宫内膜异位症罕见,但可能是广泛子宫内膜异位症的指征。该病例强调了在识别尿道下阴道子宫内膜异位症病变时进行仔细的临床检查、手术切除和腹腔镜评估的重要性。