Suburethral Endometriosis as Clinical Finding of Extensive Disease.

CRSLS : MIS case reports from SLS Pub Date : 2022-01-25 eCollection Date: 2022-01-01 DOI:10.4293/CRSLS.2021.00080
Ceana H Nezhat, Maria Hincapie, Anar Gojayev, Adi Katz
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引用次数: 1

Abstract

Objective: 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.

Methods and procedures: 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.

Results: 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.

Conclusion: 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.

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广泛疾病的临床表现:喉下子宫内膜异位症。
目的:子宫内膜异位症扩散到阴道是罕见的,只有0.02%的女性有症状的子宫内膜异位症。喉下病变部位是例外。在广泛的文献回顾中,仅发现了4例喉下子宫内膜异位症。我们的目的是报告一例31岁的阴道阴道下子宫内膜异位症患者,她接受了腹腔镜检查,并对这一主题进行了文献回顾。方法和步骤:基于从患者数据库中提取的信息进行病例报告。通过Medline检索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,对相关文献进行回顾。结果:本病例报告描述了一例31岁女性患者,因严重盆腔疼痛,在月经期间恶化。体格检查发现一个2厘米的子宫内膜异位症病变是最初的表现。她的检查也有明显的子宫和附件肿大,柔软。根据检查和影像学,怀疑子宫腺肌症和子宫内膜异位症。手术评估显示广泛子宫内膜异位症伴淋巴结累及腹腔镜探查。文献回顾显示,只有4例,其中颈椎管下子宫内膜异位症以前被确定。结论:原发性阴道尿道下子宫内膜异位症虽然罕见,但可能是广泛子宫内膜异位症的指征。这个病例强调了仔细的临床检查,手术切除和腹腔镜评估的重要性,当确定阴道下子宫内膜异位症病变。
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