VanderBrink Brian A, Sivan Bezalel, Levitt Marc A, Peña Alberto, Sheldon Curtis A, Alam Shumyle
Division of Urology, Division of Pediatric Surgery at Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio USA.
Colorectal Center for Children, Division of Pediatric Surgery at Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio USA.
Int Braz J Urol. 2014 Sep-Oct;40(5):676-82. doi: 10.1590/S1677-5538.IBJU.2014.05.13.
Epididymitis in patients with anorectal malformation (ARM) represents a unique problem because unlike the general population, an underlying urinary tract problem is frequently identified. We review our experience with epididymitis in ARM population with an emphasis on examining urologic outcomes.
We performed a retrospective review of male patients with ARM cared for from 1980 to 2010. Clinical and pathologic variables recorded included age at presentation, recurrence, associated urologic anomalies, incidence of ureteral fusion with mesonephric ductal structures, glomerular filtration rate and urodynamic parameters.
Twenty-six patients were identified with documented episodes of epididymitis. Renal injury was noted in five patients (19%), all of whom were diagnosed with neurogenic bladder (NGB) several years after anorectoplasty. NGB was found in ten patients (38%) in our series. Ectopic insertion of ureter into a mesonephric ductal structure was discovered in five patients (19%). Twelve patients (46%) had recurrent episodes of epididymitis, with seven of these patients (58%) being diagnosed with NGB. Two patients in the pubertal group presented with a history of epididymitis and complained of ejaculatory pain.
Epididymitis in a patient with ARM warrants a comprehensive urologic investigation, particularly in recurrent episodes. Attempts at surgical intervention (e.g. vasectomy) should be avoided until functional assessment of the urinary tract has occurred. Failure to recognize this association may lead to potentially avoidable complications and morbidity. Long term urological follow up of these patients is warranted to identify at risk patients and minimize renal deterioration.
肛门直肠畸形(ARM)患者的附睾炎是一个独特的问题,因为与普通人群不同,常可发现潜在的泌尿系统问题。我们回顾了我们在ARM患者中治疗附睾炎的经验,重点是检查泌尿外科治疗结果。
我们对1980年至2010年期间接受治疗的ARM男性患者进行了回顾性研究。记录的临床和病理变量包括就诊年龄、复发情况、相关的泌尿系统异常、输尿管与中肾管结构融合的发生率、肾小球滤过率和尿动力学参数。
确定有26例患者有附睾炎发作记录。5例患者(19%)出现肾损伤,所有这些患者在肛门直肠成形术后数年被诊断为神经源性膀胱(NGB)。在我们的系列研究中,10例患者(38%)发现有NGB。5例患者(19%)发现输尿管异位插入中肾管结构。12例患者(46%)有附睾炎复发,其中7例患者(58%)被诊断为NGB。青春期组的2例患者有附睾炎病史,并主诉射精疼痛。
ARM患者的附睾炎需要进行全面的泌尿外科检查,特别是在复发时。在对尿路进行功能评估之前,应避免进行手术干预(如输精管切除术)。未能认识到这种关联可能会导致潜在的可避免并发症和发病率增加。对这些患者进行长期的泌尿外科随访,以识别高危患者并尽量减少肾脏恶化。