Lamarca Marta, Navarro Ricardo, Ballesteros María Eugenia, García-Aguirre Salvador, Conte María Pilar, Duque José Antonio
Department of Assisted Reproduction, Miguel Servet University Hospital, Zaragoza, Spain.
Fertil Steril. 2009 Mar;91(3):931.e13-5. doi: 10.1016/j.fertnstert.2008.08.132. Epub 2008 Oct 18.
To describe a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome associated with bilateral myomas in uterine remnants.
Case report.
University hospital.
PATIENT(S): A 35-year-old woman with MRKH syndrome and pelvic pain, in whom leiomyomas were diagnosed by imaging techniques.
INTERVENTION(S): Diagnostic laparoscopy followed by excision of leiomyomas and uterine remnants by laparotomy.
MAIN OUTCOME MEASURE(S): Resolution of symptoms and histologic confirmation of the clinic diagnosis.
RESULT(S): After a 6-month follow-up period, the patient was asymptomatic. The histologic examination confirmed MRKH syndrome associated with multiple myomas in both rudimentary uteri.
CONCLUSION(S): This is an unusual case of MRKH syndrome associated with bilateral leiomyomas. The excision of the tumors with the adjacent uterine remnants is indicated when they are symptomatic.
描述一例 Mayer-Rokitansky-Küster-Hauser(MRKH)综合征合并子宫残端双侧肌瘤的病例。
病例报告。
大学医院。
一名 35 岁患有 MRKH 综合征且伴有盆腔疼痛的女性,通过影像学技术诊断出患有平滑肌瘤。
诊断性腹腔镜检查,随后通过剖腹手术切除平滑肌瘤和子宫残端。
症状缓解及临床诊断的组织学确认。
经过 6 个月的随访期,患者无症状。组织学检查证实为 MRKH 综合征合并双侧残角子宫多发肌瘤。
这是一例罕见的 MRKH 综合征合并双侧平滑肌瘤的病例。当肿瘤有症状时,建议切除肿瘤及相邻的子宫残端。