UTERUS DIDELPHYS WITH UNILATERAL HEMATOCOLPOS, IPSILATERAL RENAL AGENESIS AND MENSES - A CASE-REPORT AND LITERATURE-REVIEW
- 1 January 1987
- journal article
- review article
- Vol. 32 (1) , 47-58
Abstract
A 13-year-old girl with signs and symptoms of an acute abdomen was found to have uterus didelphys, unilateral hematocolpos, ipsilateral renal agenesis and menses. A review of the literature in English revealed 115 reported cases. This complex congenital anomaly is seen most commonly in adolescents with dysmenorrhea of progressive severity, adbominal pain and a pelvic mass.This publication has 10 references indexed in Scilit:
- Uterus Didelphia with Left Hematocolpos and Ipsilateral Renal AgenesisJournal of Urology, 1982
- COMPLETE DUPLICATION OF THE UTERUS AND CERVIX WITH A UNILATERALLY IMPERFORATE VAGINA1982
- DOUBLE UTERUS WITH AN UNILATERAL BLIND VAGINA - A REPORT OF 3 CASES1981
- The double uterus associated with an obstructed hemivagina and ipsilateral renal agenesisAmerican Journal of Obstetrics and Gynecology, 1980
- Uterus Didelphys with Unilateral Imperforate Vagina: A Rare Cause of Acute Urinary RetentionJournal of Urology, 1979
- Lateral communicating double uterus with unilateral vaginal obstructionAmerican Journal of Obstetrics and Gynecology, 1976
- GENITAL ANOMALIES ASSOCIATED WITH SOLITARY KIDNEY1966
- UTERUS DEDELPHYS WITH UNILATERAL IMPERFORATE VAGINA - REPORT OF 4 CASES1963
- EMBRYOLOGY OF MULLERIAN DUCT SYSTEM - REVIEW OF PRESENT-DAY THEORY1962
- UTERUS DIDELPHYS AND SEPTATE VAGINA - REVIEW - REPORT OF A CASE WITH GYNATRESIC RIGHT VAGINA AND ASSOCIATED HEMATOCELES1956