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Scholars Journal of Medical Case Reports | Volume-5 | Issue-09
Bicornuate Bicollis Uterus Presenting as Heavy Mentrual Bleeding - A Case Report
Geeta Katheit, Chaya Budhwani
Published: Sept. 30, 2017 |
153
186
DOI: 10.36347/sjmcr.2017.v05i09.006
Pages: 534-536
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Abstract
Congenital anomaly of the uterus results from varying degree of failure of fusion of the mullerian ducts. Bicornuate uterus (BU) is a congenital uterine anomaly with a prevalence of 0.4% in the general population. We report a case of 35 years old p1L1 woman who had heavy mentrual bleeding since 3-4 years. Her USG showed bicornuate uterus with bilateral normal adnexa. Failing medical management total abdominal hysterectomy with left salpingoopherectomy was done. On cut section two separate uterine cavities with two cervical canal were seen.