An incidental coexistence of Mayer-Rokitansky-Kuster-Hauser syndrome with pelvic ectopic kidney and perirenal endometrioma.
This case report details a 17-year-old patient with Mayer-Rokitansky-Kuster-Hauser syndrome incidentally found to have a pelvic ectopic kidney and a perirenal endometrioma.
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This 2008 case report describes a 17-year-old patient with primary amenorrhea in whom Mayer-Rokitansky-Kuster-Hauser syndrome coexisted with a centrally located pelvic ectopic kidney and a perirenal retroperitoneal cyst containing endometrial tissue. After imaging showed absent uterus, normal ovaries, and a large right adnexal/retroperitoneal cyst adjacent to the ectopic kidney, laparoscopy/laparotomy led to extirpation of an 8×11 cm smooth perirenal cyst, with pathology demonstrating endometrial tissue and hemorrhage. The main limitation is that, as an incidental single-patient case report, it provides no generalizable evidence beyond this unique coexistence. This paper is centrally about endometriosis—specifically a perirenal endometrioma identified in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome and pelvic ectopic kidney.
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Cited by (7)
- Age‐dependent phenotypes of ovarian endometriomas 2022
- The Presence of Endometriosis in the Human Fetus 2020
- Müllerian duct anomalies coincident with endometriosis: a review 2020
- Endometriosis in MRKH cases as a proof for the coelomic metaplasia hypothesis? 2019
- Renal endometriosis mimicking complicated cysts of kidney: report of two cases 2017
- Embryologic origin of endometriosis: Analysis of 101 human female fetuses 2011
- Pre-natal exposure of mice to bisphenol A elicits an endometriosis-like phenotype in female offspring 2010
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