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A case of vesical endometriosis associated with Wunderlich syndrome

机译:膀胱内异症合并Wunderlich综合征1例

摘要

A case of vesical endometriosis associated with unilateral renal agenesis and uterus didelphys (Wunderlich syndrome) is reported. A 20-year-old unmarried woman visited the gynecologic department with dysmenorrhea. She was referred to us because a bladder mass was detected on abdominal ultrasonography. She had no episode of gross hematuria. Cystoscopy revealed a finger tip-sized cystic mass dark red to dark blue in color. Computerized tomography and magnetic resonance imaging demonstrated right renal agenesis and uterus didelphys. The mass was located at the ureterovesical pouch and protruded into the bladder. Partial cystectomy, right hysterectomy and right salpingo-oophorectomy were performed. Histopathological diagnosis was endometriosis. The patient was treated with 400 mg danazol for 6 months has had no recurrence and regular menstruation.
机译:据报道一例与单侧肾发育不全和子宫双侧子宫相关的膀胱内膜异位症(Wunderlich综合征)。一名20岁未婚妇女因痛经来到妇科。她之所以被转介给我们,是因为腹部超声检查发现了膀胱肿块。她没有严重的血尿发作。膀胱镜检查显示出指尖大小的囊性肿块,呈深红色至深蓝色。电脑断层扫描和磁共振成像显示右肾发育不全和子宫双眼。该肿块位于输尿管囊袋处,并伸入膀胱。进行部分膀胱切除术,右子宫切除术和右输卵管卵巢切除术。组织病理学诊断为子宫内膜异位。该患者接受400 mg达那唑治疗6个月,未复发且月经规律。

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