Double urethra, double bladder, left renal agenesis, persistent hymen, double vagina, and uterus didelphys: A case report

M. Singh, J. P. Gearhart, J. A. Rock

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

A patient with a suspected mullerian anomaly was evaluated with an intravenous pyelogram (IVP), vaginoscopy, laparoscopy, cystoscopy, and vaginal exploration. The patient was noted to have a double urethra, double bladder, left renal agenesis, persistent hymen, double vagina, and uterus didelphys. She was managed conservatively with removal of the persistent hymen and vaginal septum. A review of similar anomalies is discussed and a plausible embryological explanation for this anomaly is offered.

Original languageEnglish (US)
Pages (from-to)99-101
Number of pages3
JournalAdolescent and Pediatric Gynecology
Volume6
Issue number2
DOIs
StatePublished - Jan 1 1993
Externally publishedYes

Fingerprint

Hymen
Vagina
Urethra
Uterus
Urinary Bladder
Cystoscopy
Urography
Laparoscopy
Hereditary renal agenesis

Keywords

  • Double bladder
  • Double urethra
  • Double vagina
  • Left renal agenesis
  • Persistent hymen
  • Uterus didelphys

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology

Cite this

Double urethra, double bladder, left renal agenesis, persistent hymen, double vagina, and uterus didelphys : A case report. / Singh, M.; Gearhart, J. P.; Rock, J. A.

In: Adolescent and Pediatric Gynecology, Vol. 6, No. 2, 01.01.1993, p. 99-101.

Research output: Contribution to journalArticle

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