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首页> 外文期刊>Case Reports in Obstetrics and Gynecology >Endometriosis in a Patient with Mayer-Rokitansky-Küster-Hauser Syndrome
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Endometriosis in a Patient with Mayer-Rokitansky-Küster-Hauser Syndrome

机译：Mayer-Rokitansky-Küster-Hauser综合征患者的子宫内膜异位症

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Objective. To report a case of Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) in which there were two nonfunctional rudimentary uteruses with the presence of ovarian endometrioma, corroborating that there are valid alternative theories to the existence of endometriosis, rather than Sampson’s theory alone, such as the coelomic metaplasia theory.Design. A case report.Setting. A tertiary referral center, which is also a university hospital.Patient. A fifteen-year-old patient with MRKH syndrome and endometriosis.Intervention. Laparoscopic approach for diagnostic confirmation and treatment of the endometrioma.Results. Evidence of endometriosis in a patient with no functional uterus.Conclusions. This case report and a few others that are available in the literature reinforce the possibility that coelomic metaplasia could be the origin of endometriosis. Patients with müllerian agenesis and pelvic pain should be carefully evaluated, and the presence of pelvic endometriosis should not be excluded.
机译：目的。为了报告一例Mayer-Rokitansky-Küster-Hauser综合征（MRKH），其中有两个伴有卵巢子宫内膜异位的非功能性基本子宫，证实存在子宫内膜异位症存在的有效替代理论，而不是仅凭Sampson的理论，例如腔室化生理论。病例报告。三级转诊中心，也是大学医院。患者。一名15岁的MRKH综合征和子宫内膜异位症患者。腹腔镜方法用于子宫内膜瘤的诊断确认和治疗。无功能子宫的患者子宫内膜异位的证据。结论。该病例报告和文献中的其他一些文献都增强了冠状​​化生可能是子宫内膜异位症起源的可能性。患有苗勒氏发育不全和骨盆疼痛的患者应仔细评估，不应排除骨盆子宫内膜异位症的存在。

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