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Background Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare syndrome affecting one out of 4500 women. It is characterized by utero-vaginal aplasia with normal development of secondary sexual characteristics and normal 46, XX karyotype. Case Report A 65-year unmarried female has presented with high grade endometrioid carcinoma of left ovary with capsular invasion. Discussion Ovary is usually...
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