Fujimoto V Y, Klein N A, Miller P B
Department of Obstetrics and Gynecology, University of Washington School of Medicine, Seattle, WA 98105, USA.
J Reprod Med. 1998 May;43(5):465-7.
Noncommunicating uterine horns are rare, occasionally presenting with functional endometrial cavities. Surgical removal of the noncommunicating horn is commonly performed to prevent endometriosis in these patients.
A 41-year-old woman with a unicornuate uterus and noncommunicating uterine horn presented with a three-month history of right-sided pelvic pain. She had previously undergone multiple assisted reproductive technique attempts with superovulation and supraphysiologic serum estradiol levels and no apparent symptomatology or evidence of hematosalpinx during laparoscopy. Shortly after completing a donor oocyte recipient cycle, she developed acute right-sided pelvic pain. Diagnostic laparoscopy and subsequent laparotomy confirmed a right hematosalpinx and hematometra of the noncommunicating horn, with stage III endometriosis.
Consideration of prophylactic resection of a noncommunicating uterine horn with a cavity should be considered in an asymptomatic, reproductive-age patient with this rare müllerian anomaly.
非交通性子宫角罕见,偶尔会出现功能性子宫内膜腔。通常会进行手术切除非交通性子宫角以预防这些患者发生子宫内膜异位症。
一名41岁的双角子宫合并非交通性子宫角女性,出现右侧盆腔疼痛3个月。她此前曾多次尝试辅助生殖技术,进行了超排卵且血清雌二醇水平高于生理值,腹腔镜检查时未出现明显症状或输卵管积血迹象。在完成一次供体卵母细胞受者周期后不久,她出现了急性右侧盆腔疼痛。诊断性腹腔镜检查及随后的剖腹手术证实为右侧输卵管积血及非交通性子宫角积血,并伴有III期子宫内膜异位症。
对于患有这种罕见苗勒管异常的无症状育龄患者,应考虑对有腔的非交通性子宫角进行预防性切除。