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假瘤性子宫内膜异位结节。

Pseudotumoral Endometriotic Nodule.

机构信息

Department of Obstetrics and Gynecology (Drs. Engels and Karampelas).

CHU Brugmann, Brussels, and Department of Obstetrics and Gynecology (Dr. Nisolle), CHR La Citadelle, Liege, Belgium.

出版信息

J Minim Invasive Gynecol. 2021 Dec;28(12):1973-1974. doi: 10.1016/j.jmig.2021.06.025. Epub 2021 Jul 2.

Abstract

STUDY OBJECTIVE

To demonstrate a rare case of a pediculated endometriotic nodule that was initially diagnosed as a solid adnexal mass.

DESIGN

We present a stepwise narrated demonstration of our laparoscopic technique.

SETTING

We present a case report of a patient aged 44 years, gravida 2 para 2, who was diagnosed with a solid (adnexal) mass during a gynecologic examination. She presented symptoms of dyspareunia. During a bimanual examination, 2 fixed nodules were palpated in both the uterosacral ligaments, and a mobile solid mass of 5 cm could be palpated on the right adnex. A transvaginal ultrasound showed a solid (adnexal) mass of 50 mm in diameter. The tumor marker cancer antigen 125 was normal, and after application of the International Ovarian Tumor Analysis score, the risk of malignancy was up to 39%. A complementary magnetic resonance image showed a heterogeneous solid mass of 47 × 47 × 29 mm with a differential diagnosis of a pediculated fibroma in (myxoid) degeneration vs an adnexal solid mass. A laparoscopic unilateral adnexectomy was scheduled, and the patient was informed about the risk of malignancy. The laparoscopy revealed bilateral normal adnexa, the presence of a solid pediculated mass originating from the right uterosacral ligament and 2 endometriotic nodules originating from the left and right uterosacral ligaments. The rectovaginal space was dissected, and a third deep infiltrating endometriotic nodule was revealed. The operation proceeded by the sectioning of the left uterosacral ligament below the endometriotic nodule. The posterior vaginal wall was separated from the endometriotic nodule, and after further dissection of the rectovaginal space, we arrived in a disease-free area. After opening of the right medial division of the pararectal space, the right hypogastric nerve was dissected and preserved. The solid mass was separated from the uterus, the right uterosacral ligament was excised at a distance from the nodule, and the pediculated mass was removed intact en block with the right ligament. The patient was discharged 24 hours after surgery. The postoperative period was uneventful. The definitive histology report confirmed the presence of endometriotic nodules and a solid tumor classified as a pseudotumoral endometriotic mass. This was justified by the presence of conjunctival vascular stroma including multiple endometriotic foci, the presence of cytogenic stroma of variable abundance including glands lined with a columnar epithelium, and, most important, the fact that the epithelium had no cytologic atypias.

INTERVENTIONS

Laparoscopic excision of the pseudotumoral endometriotic nodule en block with the right and left uterosacral ligaments.

CONCLUSION

Endometriosis is a complex multifactorial pathology in which several factors are involved: genetics, environmental factors, immunologic reactions, hormonal effects, and anatomic anomalies. All these factors may contribute to the creation of an inflammatory response related to immune cells, adhesion molecules, extracellular matrix metalloproteinase, and proinflammatory cytokines enhancing the formation of fibrotic tissue [1,2]. These changes may sometimes have an unusual presentation, as we are showing in this case report of a pseudotumoral endometriotic mass. This rare case should be included in the differential diagnosis of solid tumors before surgery for symptomatic patients and those who have a medical history of endometriosis.

摘要

研究目的

展示一例最初被诊断为实性附件肿块的带蒂子宫内膜异位症结节的罕见病例。

设计

我们展示了我们腹腔镜技术的分步叙述演示。

设置

我们报告了一名 44 岁、经产 2 次的患者的病例,在妇科检查中被诊断为实性(附件)肿块。她出现性交困难的症状。在双合诊检查中,在双侧子宫骶韧带中可触及 2 个固定的结节,在右侧附件可触及直径 5cm 的可移动实性肿块。经阴道超声显示直径为 50mm 的实性(附件)肿块。肿瘤标志物癌抗原 125 正常,应用国际卵巢肿瘤分析评分后,恶性风险高达 39%。补充磁共振成像显示直径为 47×47×29mm 的异质性实性肿块,鉴别诊断为带蒂纤维瘤(黏液样变性)与附件实性肿块。计划进行单侧附件切除术,告知患者恶性肿瘤的风险。腹腔镜检查显示双侧附件正常,存在源自右侧子宫骶韧带的实性带蒂肿块和源自左侧和右侧子宫骶韧带的 2 个子宫内膜异位症结节。直肠阴道间隙被分离,揭示了第三个深部浸润性子宫内膜异位症结节。手术在左侧子宫骶韧带下方的子宫内膜异位症结节处进行。将阴道后壁与子宫内膜异位症结节分离,进一步分离直肠阴道间隙后,我们进入无病区域。在右旁正中直肠间隙的内侧部分打开后,分离右下腹下神经并保留。实性肿块与子宫分离,从结节处切除右侧子宫骶韧带,完整地整块切除带蒂肿块和右侧韧带。患者在手术后 24 小时出院。术后无并发症。最终组织学报告证实存在子宫内膜异位症结节和实性肿瘤,分类为假肿瘤性子宫内膜异位症肿块。这是由结膜血管基质的存在证明的,包括多个子宫内膜异位症病灶,存在细胞遗传学基质,数量不定,包括柱状上皮衬里的腺体,最重要的是,上皮没有细胞学异型性。

干预措施

腹腔镜下整块切除带蒂的假肿瘤性子宫内膜异位症结节,并切除左右子宫骶韧带。

结论

子宫内膜异位症是一种复杂的多因素病理,涉及多个因素:遗传因素、环境因素、免疫反应、激素作用和解剖异常。所有这些因素都可能导致与免疫细胞、黏附分子、细胞外基质金属蛋白酶和促炎细胞因子相关的炎症反应增强,形成纤维组织[1,2]。这些变化有时可能表现异常,正如我们在这个假肿瘤性子宫内膜异位症肿块的病例报告中所展示的那样。对于有症状的患者和有子宫内膜异位症病史的患者,在手术前应将这种罕见病例纳入实性肿瘤的鉴别诊断。

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