Awan S R, Corbally M T, Guiney E J
Our Lady's Hospital for Sick Children, Crumlin, Dublin, Ireland.
Eur J Pediatr Surg. 1993 Aug;3(4):248-9. doi: 10.1055/s-2008-1063554.
Abdominal cystic masses in childhood are rare and despite improved imaging techniques continue to present diagnostic confusion. Typically such cystic lesions are mesenteric or intestinal in origin. However, rarer causes include cystic dilatation of a blind ending ureter. To date over 100 cases of blind ending ureters have been reported and their management described. We report on a case of non-communicating ureteric cyst associated with a blind ending ureter that recurred following percutaneous drainage and required operative resection. Although percutaneous drainage techniques have been advocated for a variety of abdominal cystic lesions, the experience gained from this case suggests that operative excision is the treatment of choice.
儿童腹部囊性肿块较为罕见,尽管影像技术有所进步,但仍会造成诊断上的混淆。通常这类囊性病变起源于肠系膜或肠道。然而,更罕见的病因包括盲端输尿管的囊性扩张。迄今为止,已报告了100多例盲端输尿管病例,并描述了其治疗方法。我们报告一例与盲端输尿管相关的非交通性输尿管囊肿,经皮引流后复发,需手术切除。尽管经皮引流技术已被推荐用于多种腹部囊性病变,但该病例的经验表明手术切除是首选治疗方法。