Troncon Júlia Kefalás, Zani Ana Carolina Tagliatti, Vieira Andrea Duarte Damasceno, Poli-Neto Omero Benedicto, Nogueira Antônio Alberto, Rosa-E-Silva Júlio César
Ribeirão Preto School of Medicine, University of São Paulo, Avenida Bandeirantes, 3900 Ribeirão Preto, SP, Brazil.
Case Rep Obstet Gynecol. 2014;2014:376231. doi: 10.1155/2014/376231. Epub 2014 Dec 30.
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.
目的。报告一例迈耶-罗基坦斯基-库斯特-豪泽综合征(MRKH)病例,该病例存在两个无功能的残角子宫且伴有卵巢子宫内膜异位囊肿,证实除了桑普森理论外,还有其他关于子宫内膜异位症存在的有效替代理论,如体腔上皮化生理论。设计。病例报告。地点。一家三级转诊中心,也是一所大学医院。患者。一名15岁患有MRKH综合征和子宫内膜异位症的患者。干预。采用腹腔镜方法进行诊断确认和治疗子宫内膜异位囊肿。结果。在无功能子宫的患者中发现子宫内膜异位症的证据。结论。本病例报告以及文献中其他一些病例报告强化了体腔上皮化生可能是子宫内膜异位症起源的可能性。对于患有苗勒氏管发育不全和盆腔疼痛的患者应进行仔细评估,不应排除盆腔子宫内膜异位症的存在。