Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is characterized by congenital agenesis of vagina, a rudimentary uterus and normal fallopian tubes and ovaries
the definitive risk of benign and malignant neoplasms development in uterine remnants and ovaries in patients with MRKH syndrome is still unknown
there have been case reports of ovarian cancer, endodermal sinus tumor of the ovary and immature teratoma that have been associated with MRKH
a case report of a dysgerminoma associated with MRKH has been described (1)
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