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一名患有 Rokitansky-Kuster-Hauser 综合征患者的子宫内膜异位症。

Endometriosis in a patient with Rokitansky-Kuster-Hauser syndrome.

作者信息

Cho Moon Kyoung, Kim Cheol Hong, Oh Sung Tack

机构信息

Department of Obstetrics and Gynecology, Chonnam National University Medical School, Gwangju, Korea.

出版信息

J Obstet Gynaecol Res. 2009 Oct;35(5):994-6. doi: 10.1111/j.1447-0756.2009.01025.x.

Abstract

Endometriosis in Rokitansky-Kuster-Hauser syndrome has been reported only once previously. We present here a case of endometrioma in a patient with Rokitansky-Kuster-Hauser syndrome. A 26-year-old patient with Rokitansky-Kuster-Hauser syndrome presented with abrupt pain in the left iliac quadrant. A mass was confirmed by sonography. Laparoscopic inspection revealed no uterus. The mass was removed laparoscopically. Endometriosis was confirmed histologically. If endometrioma in a patient with Rokitansky-Kuster-Hauser syndrome is associated with a small rudimentary unicornis uterus with a small endometrial cavity, endometriosis can be assumed to have developed by retrograde menstruation theory. Because the patient did not have a functioning endometrium, her endometrioma is assumed to have arisen from coelomic metaplasia.

摘要

罗-库-豪综合征(Rokitansky-Kuster-Hauser syndrome)合并子宫内膜异位症此前仅有过一例报道。我们在此呈现一名罗-库-豪综合征患者发生卵巢巧克力囊肿(endometrioma)的病例。一名26岁的罗-库-豪综合征患者出现左下腹突发疼痛。超声检查证实有一个肿块。腹腔镜检查发现没有子宫。通过腹腔镜手术切除了肿块。组织学检查证实为子宫内膜异位症。如果罗-库-豪综合征患者的卵巢巧克力囊肿与一个带有小子宫内膜腔的小残角单角子宫相关,那么可以假定子宫内膜异位症是根据经血逆流理论发展而来的。由于该患者没有功能正常的子宫内膜,她的卵巢巧克力囊肿被认为是由体腔化生引起的。

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