Department of Urology, Hospital Universitario Virgen de la Victoria, Campus Universitario de Teatinos, Málaga, Spain.
Arch Sex Behav. 2012 Aug;41(4):1065-8. doi: 10.1007/s10508-011-9895-1. Epub 2012 Jan 11.
We report a case of a rare congenital malformation, a urogenital sinus cyst in a young patient with non-specific symptoms for several months. A 21-year-old male presented with vague and intermittent abdominal pain. Ultrasound scan showed a retrovesical hypoechoic collection (approximately 6 cm) and left renal agenesis, compatible with a possible congenital malformation. These findings were confirmed by MRI. A laparoscopic excision of the cyst was performed with no complications. Pathology report confirmed a urogenital sinus cyst. The postoperative recovery was uneventful and the patient was discharged within 48 h. Urogenital sinus cysts are rare entities with few cases described in the literature. Imaging techniques such as ultrasound, CT or MRI may help with diagnosis. Therapeutic modalities range from observation to needle aspiration or surgical removal. In our case, we chose a laparoscopic approach to minimize morbidity and achieve an early recovery.
我们报告了一例罕见的先天性畸形病例，一名年轻患者患有几个月的非特异性症状的泌尿生殖窦囊肿。一名 21 岁男性因模糊和间歇性腹痛就诊。超声扫描显示一个位于膀胱后方的低回声包块（约 6 厘米）和左肾缺如，提示可能存在先天性畸形。这些发现通过 MRI 得到了证实。患者接受了腹腔镜下囊肿切除术，无并发症发生。病理报告证实为泌尿生殖窦囊肿。术后恢复顺利，患者在 48 小时内出院。泌尿生殖窦囊肿是一种罕见的实体，文献中仅有少数病例描述。超声、CT 或 MRI 等影像学技术有助于诊断。治疗方式包括观察、经皮穿刺抽吸或手术切除。在我们的病例中，我们选择了腹腔镜方法，以尽量减少发病率并实现早期康复。
