Abstract
We relate one observation about a rare case of genital malformation, where is on association of unilateral hematocopos, bicorn uterine and homolateral renal agenesis. The diagnostic was suspected upon the association with a progressive dysmenorrhe and vaginal mass. II was confirmed by ethnographie and IRM. The treatment has been conservative and consisted only in the section of the vaginal partition.
Publication types
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Case Reports
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English Abstract
MeSH terms
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Abnormalities, Multiple / diagnosis*
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Abnormalities, Multiple / embryology
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Abnormalities, Multiple / epidemiology
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Abnormalities, Multiple / surgery
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Adult
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Dysmenorrhea / etiology
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Female
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Hematocolpos / diagnosis*
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Hematocolpos / etiology*
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Humans
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Kidney / abnormalities*
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Magnetic Resonance Imaging
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Mullerian Ducts / embryology
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Uterus / abnormalities*
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Vagina / abnormalities*
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Wolffian Ducts / embryology