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.
Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
homolateral renal
8
[complete utero-vaginal
4
utero-vaginal duplication
4
duplication hematocolpos
4
hematocolpos homolateral
4
renal agenesis]
4
agenesis] relate
4
relate observation
4
observation rare
4
rare case
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!