Alsahabi Jawaher, Dendini Mohammad, Al-Zahrani Eman F, Alosiami Abdulaziz, Bamanie Elham
Urogynecology and Reconstructive Pelvic Surgery Division, King Abdul-Aziz Medical City Ministry of National Guard Health Affairs, Riyadh, SAU.
Obstetrics and Gynecology, King Abdullah International Medical Research Center, Riyadh, SAU.
Cureus. 2023 Feb 15;15(2):e35024. doi: 10.7759/cureus.35024. eCollection 2023 Feb.
Paraurethral endometriosis is an extremely rare condition. To the best of our knowledge, only seven cases with details on variable risk factors have been reported in the English literature. Herein, we present the case of a third nulliparous patient described in the literature at the time of diagnosis. A 30-year-old woman presented with mild urinary symptoms. A well-defined 2.3 cm paraurethral cystic lesion was found on clinical examination, and MRI findings were suggestive of hemorrhagic content, with no evidence of pelvic endometriosis. Complete surgical excision was performed, and the patient's symptoms improved. The patient experienced no recurrence for 10 months postoperatively. The histopathological findings were suggestive of endometriosis. These findings might indicate that embryonic remnants are possible causes of the pathogenesis of paraurethral endometriosis.
尿道旁子宫内膜异位症是一种极其罕见的病症。据我们所知,英文文献中仅报道了7例详细阐述了多种风险因素的病例。在此,我们呈现了一例在诊断时文献中所描述的未生育过三次的患者病例。一名30岁女性出现轻微尿路症状。临床检查发现一个边界清晰的2.3厘米尿道旁囊性病变,磁共振成像(MRI)结果提示有出血成分,且无盆腔子宫内膜异位症的证据。进行了完整的手术切除,患者症状改善。术后10个月患者未出现复发。组织病理学检查结果提示为子宫内膜异位症。这些发现可能表明胚胎残余是尿道旁子宫内膜异位症发病机制的可能原因。