Deligeoroglou Efthimios, Kontoravdis Antonios, Makrakis Evangelos, Christopoulos Panagiotis, Kountouris Apostolos, Creatsas George
Second Department of Obstetrics and Gynecology, University of Athens, Aretaieion Hospital, Athens, Greece.
Fertil Steril. 2004 May;81(5):1385-7. doi: 10.1016/j.fertnstert.2003.09.067.
To describe two cases of leiomyoma development in patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome).
Case report.
Second Department of Obstetrics and Gynecology, University of Athens, Aretaieion Hospital, Athens, Greece.
PATIENT(S): A 42-year-old woman with MRKH syndrome presented with lower abdominal pain, and a 38-year-old woman with MRKH syndrome presented with an asymptomatic left adnexal mass.
INTERVENTIONS(S): Clinical examination, transabdominal ultrasonography, IV urography, laparoscopy.
MAIN OUTCOME MEASURE(S): Ultrasound.
RESULT(S): In both cases, laparoscopy revealed a leiomyoma originating from the left uterine remnant. The leiomyomas and the adjacent uterine remnants were laparoscopically excised.
CONCLUSION(S): In rare cases, leiomyomas can originate from the fibromuscular tissue of uterine remnants in patients with MRKH syndrome.
描述两例患有迈耶-罗基坦斯基-库斯特-豪泽综合征(MRKH综合征)的患者发生平滑肌瘤的情况。
病例报告。
希腊雅典阿雷泰翁医院雅典大学妇产科第二科室。
一名42岁患有MRKH综合征的女性出现下腹部疼痛,一名38岁患有MRKH综合征的女性出现无症状的左附件肿块。
临床检查、经腹超声检查、静脉肾盂造影、腹腔镜检查。
超声检查。
在两例病例中,腹腔镜检查均发现平滑肌瘤起源于左侧子宫残端。通过腹腔镜切除了平滑肌瘤及相邻的子宫残端。
在罕见病例中,MRKH综合征患者的平滑肌瘤可起源于子宫残端的纤维肌组织。