Castellanos González L, Capdevila Hernández J M, Lanzas Prieto J M, Senén González Tuero J, González Naranjo F
Servicio de Urología, Hospital San Agustín, Avilés, Asturias, España.
Arch Esp Urol. 1996 Oct;49(8):864-7.
Herein we describe a case of an extremely uncommon malformation of the genitourinary system in a patient who had consulted for epididymitis.
Patient evaluation included radiological examination, IVP, US, CT and DVG The latter method was essential in the diagnosis of the malformation.
The findings indicated left renal agenesis with blind left ureter opening to the ipsilateral ejaculatory duct, with severe deformity of the left seminal vesicle and ejaculatory duct.
Since the patient has no important symptoms at the present time, contrary to the widely accepted approach, surgery has not been performed due to the risk of causing an iatrogenic lesion.
在此我们描述一例因附睾炎前来就诊的患者，其患有极为罕见的泌尿生殖系统畸形。
患者评估包括放射学检查、静脉肾盂造影（IVP）、超声（US）、计算机断层扫描（CT）和排尿性膀胱尿道造影（DVG）。后一种方法对畸形的诊断至关重要。
检查结果显示左肾缺如，左输尿管盲端开口于同侧射精管，左精囊和射精管严重畸形。
由于该患者目前没有重要症状，与广泛接受的方法相反，因存在造成医源性损伤的风险，未进行手术。
