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首页> 外文期刊>BMC Urology >A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management
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A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management

机译:罕见的diaphragm肌输尿管疝病例报告:内镜和开放性重建治疗

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Background Ureteral herniations are a rare occurrence, generally found incidentally on cross sectional imaging or during surgical intervention for unrelated processes. Several locations of ureteral herniations can occur including the inguinal, femoral, sciatic, obturator, and thoracic regions. While few reports of ureteral hernias are reported in the literature overall, the vast majority of those reported are inguinoscrotal herniations found during evaluation and treatment of inguinal hernias. Pelvic outlet ureteral herniations intrinsically are more common secondary to their dependent locations. Intrathoracic ureteral herniations through diaphragmatic defects are an exceptionally rare subset of ureteral herniations and have only been described sparingly. Fewer than ten case reports of diaphramatic ureteral herniations have been reported and none have described both cystoscopic management and open reconstruction. Case presentation We report the case of a 81 year old female with flank pain who was found to have idiopathic diaphragmatic hernia with incarcerated proximal ureter. She had no prior injury or surgery that explained her clinical presentation. She was initially observed and then managed conservatively with ureteral stent exchanges. Ultimately she underwent open surgical repair of her diaphragmatic hernia, reduction, resection and anastomosis of redundant proximal incarcerated ureteral segment, and nephropexy for a hypermobile right renal unit. This case report illustrates the pre- and post-operative imaging studies of a very rare intrathoracic ureteral herniation as well as surgical approach to repair. Conclusion A herniated ureter is a potential source of serious renal and ureteral complications. The thoracic herniation of ureter is the rarest of the ureteral herniations. When discovered, they should be managed to preserve renal function and prevent strangulation of the affected segment of ureter. This case report documents the treatment of a thoracic ureteral herniation with observation, conservative endoscopic management, and finally open surgical reconstruction.
机译:背景技术输尿管疝是一种罕见的疾病,通常在断层成像或不相关过程的外科手术中偶然发现。可能发生输尿管疝的几个位置,包括腹股沟,股骨,坐骨神经,闭孔和胸部区域。尽管总体上文献中几乎没有关于输尿管疝的报道,但所报告的绝大多数是在腹股沟疝的评估和治疗过程中发现的阴囊阴囊疝。盆腔出口输尿管疝本质上较继发于其依赖部位更为常见。通过diaphragm肌缺损引起的胸腔内输尿管疝是输尿管疝的极少见的子集,仅对此进行了少量描述。报道少于10例的肾盂输尿管疝的病例报道,而且都没有描述膀胱镜处理和开放重建。病例介绍我们报告了一位81岁的女性,患有侧面疼痛,该病例被发现患有特发性diaphragm疝并伴有近端输尿管嵌顿。她之前没有受伤或手术可以解释她的临床表现。最初观察到她,然后通过输尿管支架置换保守治疗。最终,她接受了diaphragm肌疝的开放性外科手术修复,多余的近端嵌顿输尿管节段的复位,切除和吻合,并为右肾功能亢进的患者进行了肾切除术。该病例报告说明了极少见的胸腔内输尿管疝的术前和术后影像学研究以及手术修复方法。结论输尿管突出可能是严重肾脏和输尿管并发症的潜在来源。输尿管胸廓疝是最罕见的输尿管疝。一经发现,应妥善保管以保持肾功能,并防止受累输尿管节段被绞死。该病例报告通过观察,保守的内窥镜处理以及最后的开放式手术重建来治疗胸腔输尿管疝。

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