Asabe Shashikant, Gavade Ashish, Sabale Vilas P
Urology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Cureus. 2024 Nov 8;16(11):e73294. doi: 10.7759/cureus.73294. eCollection 2024 Nov.
Congenital anomalies are not regularly seen in day-to-day practice. Crossed fused renal anomalies are even rarer. A 50-year-old female patient presented with right-sided pain in the abdomen with intermittent episodes of burning micturition. The patient was a known case of Mayer-Rokitansky-Kuster-Hauser syndrome. X-ray of the kidney, ureter, and bladder showed right-sided renal calculus. Computed tomography showed non-visualization of the left kidney in the left renal fossa but was crossed over to the right kidney with right renal pelvic calculus. A diagnosis of crossed fused kidney with calculus disease was made. Percutaneous nephrolithotomy was performed. With advancements in minimally invasive surgeries and imaging techniques, such large renal calculus in anomalous kidneys can be managed with good results.
先天性异常在日常临床实践中并不常见。交叉融合肾异常则更为罕见。一名50岁女性患者出现右侧腹部疼痛,并伴有间歇性尿痛。该患者是一名已知的迈耶-罗基坦斯基-库斯特-豪泽综合征患者。肾脏、输尿管和膀胱的X线检查显示右侧肾结石。计算机断层扫描显示左肾窝处左肾不显影,但与右侧肾脏交叉,右侧肾盂有结石。诊断为交叉融合肾合并结石病。进行了经皮肾镜取石术。随着微创手术和成像技术的进步,这种异常肾脏中的大肾结石可以得到很好的治疗效果。