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子宫内膜异位症导致的血尿。

Hematoureter due to endometriosis.

机构信息

Atlanta Center for Minimally Invasive Surgery and Reproductive Medicine, Atlanta, Georgia.

Atlanta Center for Minimally Invasive Surgery and Reproductive Medicine, Atlanta, Georgia.

出版信息

Fertil Steril. 2014 Jun;101(6):e37. doi: 10.1016/j.fertnstert.2014.02.049. Epub 2014 Mar 26.

Abstract

OBJECTIVE

To report the laparoscopic management of a rare case of hematoureter due to endometriosis in a young woman with multiple genitourinary anomalies.

DESIGN

Video demonstration of a surgical technique and review of genitourinary endometriosis.

SETTING

Hospital.

PATIENT(S): A 17-year-old nulliparous woman with multiple genitourinary anomalies presented with pelvic pain and unilateral retroperitoneal mass. The patient had uterine didelphys, a history of left nephrectomy, and partial ureter resection as an infant. She had a partial resection of a left transverse vaginal septum due to hematocolpos at age 12. A preoperative magnetic resonance imaging (MRI) scan revealed a left retroperitoneal mass with extension to the paravesical region, reaccumulation of the hematocolpos behind the partially resected left transverse vaginal septum, and a dilated left uterine horn with hematometra.

INTERVENTION(S): Laparoscopic management of hematoureter due to intrinsic endometriosis.

MAIN OUTCOME MEASURE(S): Intraoperative findings showed uterus didelphys with dilated left horn, normal right horn, and normal right and left fallopian tubes and ovaries. The left transverse vaginal septum was resected vaginally, and the hematocolpos and hematometra drained. The left uterine horn and cervix were laparoscopically resected. The left-side serpiginous retroperitoneal mass was dissected from the pelvic sidewall, ligated, and transected, with spillage of thick, brown liquid. The pathology of the mass wall was smooth muscle and transitional epithelium consistent with ureter, in addition to hemorrhage and glandular structures consistent with endometriosis. Endometriosis was also present in the serosa of the left uterine horn. Thus, the left retroperitoneal mass was the left ureter remnant, which acquired endometriosis and collected menstrual debris, resulting in hematoureter.

CONCLUSION(S): Two major pathologic types of ureteral endometriosis have been described: intrinsic, as occurred in this patient, and extrinsic. Women with müllerian anomalies, vaginal obstruction, or imperforate hymen are at higher risk of endometriosis. Prior urogenital surgery can further complicate and distort the anatomy. Thus, a preoperative understanding of the patient's urogenital anomalies is important to consider the differential diagnoses and anticipate surgical needs.

摘要

目的

报告一例罕见的子宫内膜异位症致血尿输尿管的腹腔镜治疗。

设计

手术技术的视频演示及妇科泌尿生殖系子宫内膜异位症的回顾。

设置

医院。

患者

一名 17 岁的未婚未育妇女,有多种泌尿生殖系统异常,表现为盆腔疼痛和单侧腹膜后肿块。患者有双子宫,曾于婴儿期行左肾切除术和部分输尿管切除术,12 岁时因阴道横隔完全性闭锁行阴道横隔部分切除术。术前磁共振成像(MRI)扫描显示左腹膜后肿块延伸至旁矢状区,部分切除的左侧横隔阴道后血肿再次积聚,左子宫角扩张伴积血。

干预

腹腔镜治疗内在性子宫内膜异位症引起的血尿输尿管。

主要观察指标

术中发现双子宫,左子宫角扩张,右子宫角正常,双侧输卵管和卵巢正常。阴道横隔完全性闭锁行阴道横隔切除术,引流积血和积血。腹腔镜切除左子宫角和宫颈。左侧蛇形腹膜后肿块从骨盆侧壁分离、结扎和横断,有大量棕色粘稠液体溢出。肿块壁的病理为平滑肌和移行上皮,与输尿管一致,还有出血和与子宫内膜异位症一致的腺体结构。左子宫角的浆膜也有子宫内膜异位症。因此,左侧腹膜后肿块是左输尿管残端,获得了子宫内膜异位症并收集了月经碎片,导致血尿输尿管。

结论

已描述了两种主要的输尿管子宫内膜异位症病理类型:内在型,如本例患者;和外在型。有米勒管畸形、阴道梗阻或处女膜闭锁的妇女发生子宫内膜异位症的风险较高。先前的泌尿生殖系统手术可进一步使解剖结构复杂化和变形。因此,术前了解患者的泌尿生殖系统异常对于考虑鉴别诊断和预期手术需求很重要。

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