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A case of juvenile vesical endometriosis with unilateral renal agenesis and bicornate uterus

机译:青少年膀胱内膜异位伴单侧肾发育不全和双角子宫一例

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摘要

A case of vesical endometriosis with unilateral renal agenesis is reported. A 13-year-old girl complained of difficulty in urination and lower abdominal pain during the menstruation. Detail urological examinations revealed left renal agenesis and intravesical cystic mass. The mass was located in the left vesical lateral wall, obstructing the vesical outlet and containing dark-brown-coloured fluid in it. She finally suffered from urinary retention following the menstruation and underwent a resection of the mass together with a part of the vesical wall. During the operation, the uterus was found to be a bicornate one. The resected mass was diagnosed as an endometriosis based on the histological findings. Eighteen months after the operation she is free from any symptoms during the menstruation and recurrence of endometriosis.
机译:膀胱内膜异位症合并单侧肾发育不全的报道。一名13岁女孩抱怨月经期间排尿困难和下腹部疼痛。详细的泌尿科检查发现左肾发育不全和膀胱内囊性肿块。该肿块位于左侧膀胱侧壁,阻塞了膀胱出口,并在其中包含了暗褐色的液体。月经后,她最终遭受尿suffered留,并切除了肿块和部分膀胱壁。手术中发现子宫是双角形的。根据组织学检查结果,切除的肿块被诊断为子宫内膜异位。术后十八个月,她在月经和子宫内​​膜异位症复发期间没有任何症状。

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