BICORNUATE UTERUS WITH CERVICAL ATRESIA AND VAGINAL AGENESIS ASSOCIATED WITH OVARIAN ENDOMETRIOSIS - A CASE REPORT
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This case report describes a 29-year-old woman with a bicornuate uterus, cervical atresia, and vaginal agenesis who presented with severe endometriosis, highlighting the association between these Mullerian duct anomalies and progressive ovarian endometriosis.
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Abstract
Vaginal agenesis combined with a functional uterus is a rare type of Mullerian duct anomaly. Only 7-8% of patients with vaginal agenesis have a functional uterus. Women born with vaginal agenesis, cervical atresia combined with a functioning endometrium typically present with hematometra, disabling pelvic pain and progressively worsening endometriosis. Almost all need an abdominal hysterectomy for relief. We report a case of severe endometriosis in a 29 years old woman having a bicornuate uterus with cervical atresia and vaginal agenesis.
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