Author/Authors :
Al-Jaroudi, Dania H. King Fahad Medical City - Women’s Specialized Hospital - Department of Reproductive Medicine Unit, Minimally Invasive Gynecologic Surgery,, Saudi Arabia , Nasser, Ayda M. King Fahad Medical City - Women’s Specialized Hospital - Department of Obstetrics and Gynecology, Saudi Arabia
Abstract :
Mayer-Rokitansky-Kuster-Hauser Syndrome in association with hyperprolactinemia is very rare. An 18-year-old, Saudi, single, virgin female was accompanied by her mother seeking medical advice regarding absent menses. She had normal breasts, normal axillary and pubic hair, normal vulva, urethra, and labial folds, however, the vagina was blind, approximately 2 cm length. Pelvic magnetic resonance imaging showed normal appearing ovaries, a small uterus and small cervix and vagina. Investigations showed initial high serum prolactin of 1,517 mIU/L. Cranial MRI was normal. The patient was diagnosed as mullerian hypoplasia class I American Fertility Society. After an extensive literature search, we present a unique case of concomitant occurrence of MRKH, in the form of mullerian hypoplasia, and hyperprolactinemia.
