| Literature DB >> 23042009 |
Murat Mermerkaya1, Berk Burgu, Nurullah Hamidi, Seher Yüksel, Zeynep B Özçakar, Ayşe Sertçelik, Fatoş Yalçinkaya, Tarkan Soygür.
Abstract
Mayer-Rokitansky-Küster-Hauser anomaly originates from agenesis of the Müllerian duct including agenesis of the uterus and the vagina because of abnormal development of the uterine ducts. This syndrome may be accompanied by the upper urinary tract anomalies such as unilateral renal agenesis, ectopia of 1 or both kidneys, renal hypoplasia, horseshoe kidney, and hydronephrosis. We report a 16-year-old girl, with unilateral renal agenesis, herniating ovary, and renal cell carcinoma in her solitary kidney, associated with Mayer-Rokitansky-Küster-Hauser syndrome-the first case in the literature to our knowledge.Entities:
Mesh:
Year: 2013 PMID: 23042009 DOI: 10.1097/MPH.0b013e3182707321
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289