Open AccessA Rare Case of Recurrent Vaginal Wall Abscess in Communicating Bicornuate Uterus with Renal Agenesis
Author(s) -
Deepti Shrivastava,
Sindhu Bhute,
Deepika Rani,
Shatavisa Mukherjee
Publication year - 2011
Publication title -
journal of south asian federation of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.108
H-Index - 8
eISSN - 0975-1920
pISSN - 0974-8938
DOI - 10.5005/jp-journals-10006-1119
Subject(s) - bicornuate uterus , medicine , uterus didelphys , presentation (obstetrics) , cervix , agenesis , renal agenesis , gynecology , mullerian ducts , infertility , uterus , pregnancy , surgery , kidney , cancer , biology , genetics
Clinical presentation of müllerian anomalies vary widely. We are reporting here a case of müllerian anomaly, had suffered from secondary infertility and purulent vaginal discharge for last two years. After thorough clinical examination and systematic investigations, her proper diagnosis of communicating bicornuate uterus (H shaped) with partial agenesis of left cervix and total agenesis of right cervix and right kidney was made and patency of right tube was restored, so that not only her symptoms were resolved but she had successful pregnancy too.