中肾囊肿性子宫内膜瘤:不典型部位子宫内膜异位症的外科治疗。

CRSLS : MIS case reports from SLS Pub Date : 2023-10-06 eCollection Date: 2023-07-01 DOI:10.4293/CRSLS.2023.00029
Ripal Madnani, Sandip Sonara
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引用次数: 1

摘要

目的:起源于中肾囊肿的子宫内膜异位症是不寻常的,患病率未知。wolffian管残余(中肾囊肿)的子宫内膜异位病变是例外。在扩展的文献综述中,动物研究中只报告了三例病例,我们在这里报告的病例是人类中的第一例。我们报告了一例37岁的中肾囊肿子宫内膜异位瘤患者,该患者因严重痛经、长期骨盆和背部疼痛、生育能力低下、严重性交困难和腹股沟不适而转诊。患者接受了腹腔镜切除术,我们进行了文献综述,以了解非典型部位子宫内膜异位症的起源和手术治疗。方法和程序:病例报告基于从患者数据库中获得的信息。我们使用Medline搜索进行了文献综述,关键词为:中肾囊肿子宫内膜异位症、wolffian管残余物中子宫内膜异位的非典型位置和Gartner管囊肿子宫内膜瘤。结果:体检发现左侧附件充盈、压痛,左侧阴道侧壁充盈,子宫活动受限。根据检查和影像学检查,怀疑为左卵巢囊肿和中肾囊肿。手术探查发现左侧出血性囊肿伴深浸润性子宫内膜异位症,累及左侧输尿管,左侧子宫骶骨韧带伴中肾囊肿伴子宫内膜异位。文献回顾显示,在雌性狗中发现了3例中肾囊肿残留的异位子宫内膜组织。结论:中肾囊肿子宫内膜异位瘤虽然罕见,但可作为广泛性子宫内膜异位症的代表。该病例强调了仔细的临床检查、患者症状与检查和影像学的相关性以及成功腹腔镜治疗非典型位置子宫内膜异位病变的重要性。我们完成了关于此类病例成功手术治疗的文献综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mesonephric Cyst Endometrioma: Surgical Management of an Atypical Site Endometriosis.

Mesonephric Cyst Endometrioma: Surgical Management of an Atypical Site Endometriosis.

Mesonephric Cyst Endometrioma: Surgical Management of an Atypical Site Endometriosis.

Objectives: Endometriosis originating in mesonephric cyst is unusual and with unknown prevalence. Endometriotic lesion in vestigial remnant of wolffian duct (mesonephric cyst) is exceptional. In the extended literature review only three cases have been reported in animal studies, and our case reported here is the first in human beings. We present a case of mesonephric cyst endometrioma in a 37-year-old patient who was referred for severe dysmenorrhea, long duration pelvic and back pain, subfertility, severe dyspareunia, and groin discomfort. The patient underwent laparoscopic removal and we performed a literature review to gain insight about the origin and surgical management of an atypical site endometriosis.

Methods and procedures: Case report presentation rests on information obtained from the patient database. We performed the literature review using a Medline search with the keywords: mesonephric cyst endometriosis, atypical location of endometriosis in vestigial remnant in wolffian duct, and Gartner duct cyst endometrioma.

Results: On physical examination, fullness and tenderness in left adnexa and lateral vaginal wall fullness on left side with restricted mobility of uterus was noted. Based on the examination and imaging the left ovarian cyst and mesonephric cyst were suspected. Surgical exploration revealed the left hemorrhagic cyst with deep infiltrating endometriosis involving left ureter and left uterosacral ligament with mesonephric cyst endometriosis. The review of literature revealed three cases where ectopic endometrial tissue in mesonephric cyst remnant was found in female dogs.

Conclusion: Mesonephric cyst endometrioma, although rare, can be a representative of extensive endometriosis. This case highlights an importance of careful clinical examination, correlation of patient symptoms with examination and imaging, and successful laparoscopic management of an atypical location endometriotic lesions. We completed the literature review on successful surgical management of such cases.

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