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作 者:王超[1] 吴文元[1] 田升日[1] WANG Chao;WU Wenyuan;TIAN Shengri(Department of Urology,Yanbian University Hospital,Yanji,Jilin,133000,China)
机构地区:[1]延边大学附属医院泌尿外科,吉林延吉133000
出 处:《临床泌尿外科杂志》2024年第10期936-938,共3页Journal of Clinical Urology
摘 要:输尿管异位开口是泌尿外科一种罕见的先天发育畸形,常伴有重复肾、重复输尿管畸形,单纯输尿管异位开口少见;输尿管末端囊肿同为泌尿系畸形性疾病,囊肿可在膀胱内,也可在膀胱外,以膀胱内多见,末端呈球状膨大,双侧输尿管异位开口合并输尿管末端囊肿在国内外未见报道。我院于2022年6月收治了1例双侧输尿管异位开口合并右输尿管末端囊肿患者,结合2种罕见泌尿外科畸形疾病的文献复习,现报告如下。Ectopic ureteral orifice is a rare congenital malformation of the urinary system,which is often accompanied by double kidney and repeated ureteral deformities,and simple ectopic ureteral orifice is rare.Blind ectopic ureterocele is also a malformed disease of the urinary system.It can be in the bladder,can also be outside the bladder,in the bladder is more common,and the end of the bladder can exhibit spherical dilatation.Ectopic ureteral orifice combined with blind ectopic ureterocele has not been reported at home and abroad.In June 2022,our hospital treated a patient with ectopic ureteral orifice and right blind ectopic ureterocele.The related literature of two rare urological malformations was reviewed.The case report is as follows.
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