Abstract
We report a case of uterine duplicity with blind hemivagina, hematocolpos and ipsilateral renal agenesis that manifested in adulthood with a cystic lesion in the pelvis. Uterine duplicity is a mesonephric or Wolffian anomaly inducing alterations in the fusion and resorption of the Müllerian duct during embryonic development, resulting in the presence of blind hemivagina and ipsilateral renal agenesis.The clinical manifestations of these anomalies are highly varied and range from asymptomatic patients, with good obstetric outcomes, as in the present case, to women with dramatic symptoms and extremely poor reproductive prognosis.
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