[Complete utero-vaginal duplication with hematocolpos and homolateral renal agenesis].

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.

• Authors: Aissia Nizar Ben, Sami Battar, Med F Gara
• Journal: La Tunisie medicale (Tunis Med) Vol. 80 Issue 6 Pg. 356-8 (Jun 2002) ISSN: 0041-4131 [Print] Tunisia
• Vernacular Title: Duplicité utéro-vaginale complète avec hematocolpos et agénésie rénale homolatérale.
• PMID: 12534051 (Publication Type: Case Reports, English Abstract, Journal Article)

Topics

• Abnormalities, Multiple (diagnosis, embryology, epidemiology, surgery)
• Adult
• Dysmenorrhea (etiology)
• Female
• Hematocolpos (diagnosis, etiology)
• Humans
• Kidney (abnormalities)
• Magnetic Resonance Imaging
• Mullerian Ducts (embryology)
• Uterus (abnormalities)
• Vagina (abnormalities)
• Wolffian Ducts (embryology)