Radu V D, Bercea B
Clinica de Urologic si Transplant Renal, Spitalul "Dr. C.I. Parhon" Iaşi.
Rev Med Chir Soc Med Nat Iasi. 2009 Oct-Dec;113(4):1151-4.
Bilateral ureterocele is a rare congenital condition that is usually diagnosed antenatally or in childhood. We present the case of a 64 year-old woman who was admitted for incidentally discovered microscopic hematuria. A bilateral ureterocele and secondary pelvic ureteral calculi were diagnosed by clinical examination (vaginal touch), ultrasound, plain radiography and intravenous urography. A transurethral incision of the ureterocele and extraction of calculi was performed by endoscopic approach. The postoperative recovery was uneventfull. Considering the risk for development of vesicoureteral reflux or recurrence of obstruction at the ureterovesical junction, a close long-term follow-up is required.
双侧输尿管囊肿是一种罕见的先天性疾病，通常在产前或儿童期被诊断出来。我们报告一例64岁女性患者，因偶然发现镜下血尿入院。通过临床检查（阴道触诊）、超声、腹部平片和静脉肾盂造影诊断为双侧输尿管囊肿及继发性盆腔输尿管结石。采用内镜方法行经尿道输尿管囊肿切开术及结石取出术。术后恢复顺利。考虑到存在膀胱输尿管反流或输尿管膀胱连接处梗阻复发的风险，需要进行密切的长期随访。
