Prakash Priyanka R, Rathan Vipul K, Rai Santosh Phajir Vishwanath
Department of Radiodiagnosis, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, India.
Radiol Case Rep. 2025 Oct 24;21(1):290-296. doi: 10.1016/j.radcr.2025.09.077. eCollection 2026 Jan.
Bladder duplication is a rare congenital anomaly, seldom reported in adults. We describe a young male presenting with recurrent urinary symptoms and lower abdominal pain. Imaging (ultrasound, CT urogram, MRI) revealed a complete sagittal septum dividing the bladder into 2 cavities with cystolithiasis, along with a hypoplastic left kidney, vesicoureteral junction (VUJ) diverticulum, partial sacral hypoplasia, and hypoplastic prostate and seminal vesicles. The patient underwent septum resection and stone removal, leading to symptom resolution. This case underscores the importance of considering congenital anomalies in adult urological presentations and highlights the role of comprehensive imaging in diagnosis and management.
膀胱重复畸形是一种罕见的先天性异常，在成人中鲜有报道。我们描述了一名年轻男性，他反复出现泌尿系统症状和下腹部疼痛。影像学检查（超声、CT尿路造影、MRI）显示，一个完整的矢状隔将膀胱分为两个腔，并伴有膀胱结石，同时还有左肾发育不全、膀胱输尿管连接部（VUJ）憩室、部分骶骨发育不全以及前列腺和精囊发育不全。患者接受了隔切除术和结石清除术，症状得以缓解。该病例强调了在成人泌尿外科疾病表现中考虑先天性异常的重要性，并突出了综合影像学在诊断和治疗中的作用。
